field_job_employment_type

job_industry

field_job_occupational_field_parents_all

job_organization_name

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position SummaryThe PDO Business Operations Team is seeking a highly motivated and experienced Business Operations Leader to join our team. The Director of Product Development (PD) Operations, reporting into the Senior Director of PDO Business Operations, will be part of a small, collaborative team focused on answering key business questions across the enterprise.&nbsp; In this role, the Director of PD Operations is responsible for the creation, development, and deployment of a global and comprehensive Continuous Improvement (CI) strategy for Product Development (PD), across all functions, modalities, and sites.&nbsp; The director will define the value proposition for CI within a research environment and among a diverse scientific community within PD. The director will also lead the development and implementation of operational excellence (OpEx) programs and strategies, through close partnership with senior leaders across PD, Global Product Development &amp; Supply, and other BMS divisions to align on and deliver short and long-term financial and strategic goals. The director plays a crucial role in enhancing processes, ensuring efficiency, and maintaining high standards of quality.&nbsp; The director also serves as the matrix leader for all CI and OpEx strategies and initiatives across PD.Key Responsibilities<ul><li>Accountable for the creation and development of a global PD Continuous Improvement (CI) strategy, in alignment with PD’s goals and objectives. Defines and implements programs to deploy the strategy.</li><li>Leads CI projects focused on process optimization.&nbsp; Identify, analyze, and improve existing processes to enhance efficiency, reduce waste, and increase productivity.&nbsp; Drive implementation of CI via matrix teams.</li><li>Establish CI performance metrics and benchmarks to measure the success of improvement initiatives.</li><li>Serves as the PD key point of partnership for the GPS OpEx group for alignment on strategies, best practices, training and support models. Serves as a core member of the GPS Operational Excellence (OpEx) community of practice. Translates and prioritizes GPS OpEx objectives in alignment with PD goals and objectives.</li><li>Develops and nurtures a CI and OpEx mindset across the global PD community.&nbsp; Coaches and mentors CI leaders within the PD functions. Develops and delivers training programs to educate employees on CI methodologies and best practices.</li><li>Drive stakeholder management through effective communication focused on gaining stakeholder buy-in and support for CI efforts.&nbsp;</li><li>Interacts with senior leader to deliver strategies and goals across R&amp;D, GDD, GPS, PD LT and PD SLT.&nbsp; Communicate progress, challenges, and success to senior management and other stakeholders.</li></ul>Qualifications &amp; Experience<ul><li>Bachelor’s degree in engineering, Life Sciences, Pharmacy, Business Administration, or relevant scientific discipline.&nbsp; Advanced degree (MBA or equivalent) a plus.&nbsp; Lean Six Sigma Certification a plus.</li><li>Significant experience (15+ years) in the pharmaceutical, biotechnology, or life sciences industry, with a strong understanding of pharmaceutical development processes.</li><li>Proven experience (5+ years) in leading CI and OpEx transformations, initiatives, process optimization, and implementing methodologies. Business Process Management (BPM) experience a plus.</li><li>Strong influencing/persuasive skills with a demonstrated ability to influence different styles at different levels in organization.&nbsp; Demonstrated ability to successfully influence and interact with senior leaders.</li><li>Experience with matrix leadership, project management, and managing stakeholders at all levels.&nbsp;</li><li>Excellent cross functional communications skills and a decisive yet collaborative leadership style.</li><li>Strong analytical and problem-solving skills.</li></ul>#GPSProdDevIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb

Director, PD Operations (Continuous Improvement)

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position SummaryThe Senior Director of Clinical Quality Audit strategy is responsible for defining the development and implementation of audit strategy for all clinical processes, vendors and therapeutic areas. The position provides leadership for the identification and resolution of critical quality risks and issues that may affect BMS. The Senior Director, Clinical Quality Audit strategy is also responsible for effectively engaging with Strategic Sourcing, Procurement and other key stakeholders in BMS. The Senior Director will partner with internal and external vendors to promote a culture of quality, risk management and compliance excellence. The Senior Director will also play a crucial role in assessing, managing and integrating quality throughout mergers, acquisitions and integrations.Key Responsibilities:<ul><li>Define and lead the strategic vision for Clinical Processes and Clinical Vendor Oversight, aligning it with organization goals and regulatory expectations to support high quality clinical trial execution.</li><li>Oversee vendor quality oversight activities and manage external quality (e.g., quality agreements with vendors).</li><li>Oversee GCP process quality oversight activities.</li><li>Oversee the incorporation of new technology and innovation in clinical trials ensuring reliability of trial results.</li><li>Design and implement the Clinical Audit Strategy for various Therapeutic Areas.</li><li>Partner with Risk, Governance, Operations (RGO) in the development of the Quality Narrative, in particular with contributions for the audit and inspection portion.</li><li>Design and develop a risk-based audit program.</li><li>Oversee due diligence, integration and/or acquisition activities.</li><li>Incorporate global regulatory trends and changes into the organization as applicable.</li><li>Promotes high standards of quality, compliance, and process excellence through oversight of procedure development/enhancement as well as by leading or contributing to strategic initiatives to ensure delivery of business goals.</li><li>Engage with RGO and cross functional business partners to identify areas of greatest compliance risk and obtain information and feedback relevant to process improvement and lead issue resolution.</li><li>Continually evaluate the strategic approach, drive changes in RDQ processes, and modify the RDQ program to meet the changing needs of the organization, regulatory environment and industry best practice</li><li>Ensure rapid communication of quality issues, to business partners and senior management</li><li>Act as the primary quality representative in high level discussions with vendors and other external stakeholders, addressing complex issues and negotiating resolutions.</li><li>Lead the development of quality integration plans for newly acquired entities, coordinating closely with GQ and R&amp;D.</li></ul>Qualifications &amp; Experience:<ul><li>University Graduate, Advanced life Sciences degree preferred. Equivalent relevant professional experience may be considered.</li><li>Minimum 10 years QA experience or relevant experience in medical quality management, biomedical science, clinical development, or regulatory compliance</li><li>Demonstrated strong knowledge of ICH/GCP, data integrity, regulatory guidelines/directives, clinical research processes and principles of Quality Assurance</li><li>Proven track record of building/ maintaining high-performance teams/organizations and influencing/ motivating global teams to achieve results—delivering on business and program goals</li><li>Exemplary leadership / influence management skills with ability to foster partnerships in the matrix organization across functional/ geographic/ cultural/partner boundaries</li><li>Broad understanding of digitalization including AI, automation, natural language processing</li><li>Communicates a clear and compelling vision and strategy for the business</li><li>Demonstrated experience with budgeting and planning</li><li>Extensive experience in regulatory inspection preparation, management, and related follow-up</li><li>Strong understanding of financial/budgeting and resourcing principles and utilization of this knowledge to make sound business decisions</li><li>Demonstrated analytical and conceptual capability—including capacity to develop/translate long-range strategic plans into short-range operational processes/systems/goals and ability to make sound decisions/recommendations with global perspective</li><li>Proven problem-solving skills to prevent and overcome complex process and quality related issues during clinical program implementation and execution</li></ul>#LI-HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior Director, Clinical Quality Audit Strategy

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position Summary: The Manager, U.S. Label &amp; Launch Operations, USPI Production is responsible for managing the operational processes associated with USPI production in the U.S. market. This role will drive and execute production of the U.S. Prescribing Information and all derivative documents across therapeutic areas to ensure compliance with prescribing information and FDA guidelines.The role works closely with the Proofreading team, Labeling Operations, Commercial Regulatory Affairs, and Worldwide Commercialization Excellence (WCE) on execution of all label updates and launches.The role will be part of a team responsible for the seamless implementation of prescribing information and all derivative labeling documents across all brands.&nbsp;This is an important role within U.S. Commercialization Strategy &amp; Operations Organization and key to Bristol Myers Squibb’s ambition to continue advancing the efficient and expeditious execution of launch and label update operations. In this position, this individual will report directly to the Associate Director, U.S. Label &amp; Launch Operations.Key Responsibilities:<ul><li>Drive the creation of InDesign layouts of USPI documents to ensure all follow FDA and BMS regulations and Brand guidelines.&nbsp;</li><li>Develop Photoshop versions of labeling documents per specifications.&nbsp;</li><li>Develop artwork and illustrations as required for Global Regulatory, Packaging, and R&amp;D.&nbsp;</li><li>Develop and maintain Universal Patient Language Important Safety Information aligned with Brand guidelines and UPL ISI templates.&nbsp;</li><li>Manage multiple projects in tandem and with expedited timing.&nbsp;</li><li>Deliver materials with the utmost quality, while implementing content updates with meticulous eye for detail.&nbsp;</li><li>Develop and maintain strong relationships with key stakeholders.&nbsp;</li><li>Partner with Proofreading team to ensure documents are consistent with regulations and error-free.&nbsp;</li><li>Remediate all U.S. Prescribing Information PDFs for ADA compliance to post to digital platforms.&nbsp;</li><li>Identify opportunities for efficiency and communicate with leadership areas for improvement.&nbsp;</li><li>Develop subject matter expertise in all production areas supported by USPI Production.&nbsp;</li><li>Troubleshoot problem files or processes for seamless support.&nbsp;</li><li>Develop expertise in all guidelines and requirements of USPI Production.&nbsp;</li></ul>Qualifications &amp; Experience:<ul><li>&nbsp;Expertise in Adobe Creative Suite.</li><li>Familiarity with Figma and XD.</li><li>Exemplary skills in remediating complex PDFs.&nbsp;</li><li>Meticulous eye for detail and long-term experience in the InDesign creation of mechanicals with heavy text.&nbsp;</li><li>Experience working in a multi-channel environment and ability to work in a matrix team setting</li><li>Ability to navigate complex and continually evolving organizational environments.</li><li>Strong written and verbal communication and presentation skills.</li><li>Ability to work on multiple projects with competing deadlines.&nbsp;</li><li>Experience working with leadership and communicating directly with senior leaders.&nbsp;</li><li>Ability to learn new technology and systems quickly.</li><li>Pharmaceutical experience required.</li><li>Expert in complex PDF remediation.</li><li>Minimum of 10 years of production experience required </li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Manager, U.S. Label & Launch Operations, USPI Production

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position SummaryThe Director of RDQ Operations and Performance Management will primarily be responsible for setting strategic direction and shaping the function by working closely with Global Quality, Global Product Development &amp; Supply (GPS), and Drug Development (DD) to ensure RDQ is well-positioned for long-term growth and success.Will ensure RDQ delivers on Global Quality strategies and initiatives in alignment with overall GPS and DD Strategies.&nbsp;Key Responsibilities<ul><li>Set strategic direction and lead the development of R&amp;D Quality roadmap (final accountability to deliver on the objectivesresides with respective RDQ Pillar Heads) focused on pipeline, performance, and people.</li><li>This will require working closely with senior leaders across GQ, GPS, DD, Early Research, and the R&amp;D Quality Leadership Team.&nbsp;</li><li>Leadthe development and oversight of R&amp;D Quality performance metrics to ensureeffective consolidation and communication to GQ, GPS, DD andEarly Research, as applicable.</li><li>Serve as the primary liaison for Global Quality, Strategy and Business Excellence (SBE), and the Drug Development, Portfolio &amp; Strategy teams to ensure RDQ successfully executes strategic initiatives and projects.</li><li>Create a comprehensive plan that outlines the scope, timeline, resources, and key milestones for strategic initiatives taking into consideration potential risk and mitigations.</li><li>Sets goals for RDQ that are specific, measurable, achievable, relevant, and aligned to the broader GQ/GPS and BMS strategies, and time bounded.&nbsp;</li><li>Foster cross-functional collaboration by working closely with the SB&amp;E pillars, including digital strategy, culture and people, business operations, program management, learning and OpEX.&nbsp;</li><li>Provide coordination and support for R&amp;D Quality Leadership Team meetings, ensuringrigor in cadence, agenda, actions and follow-up.</li><li>Responsible for the oversight and management of R&amp;D Quality Budget and Headcount.</li><li>Work closely with other senior leaders to identify opportunities for growth and improvement, and to ensure that the organization is aligned with its overall mission and goals.</li></ul>Other<ul><li>Champion a Quality Mindset and oversee strategic planning processes such as setting clear initiatives, developing strategic plans, engaging stakeholders, allocation of resources, assigning clear responsibilities, communication, risk management, continuous improvement, etc.&nbsp;</li><li>Provide leadership for program governance, operations, and benefits realization such as but not limited to; successful attainment and utilization of the intended advantages, outcomes, or gains that were identified as part of the project objectives.&nbsp;</li><li>Encourage a culture of continuous improvement and innovation within the pillar and each strategic initiative to adapt to evolving industry trends and challenges.&nbsp;</li><li>Lead communication efforts and serve as a role model for company values.&nbsp;</li><li>Maintaining adoption, connectivity, and alignment with GPS, GQ, DDand Early Research &amp; cross-functional partnership with key stakeholders such as Finance, HR, External Engagement, BIT, Communication, and Change Management.&nbsp;</li><li>Establish strong partnerships with business stakeholders.&nbsp;</li><li>Lead multidisciplinary or cross-functional work/project teams; serve as part of strategic team(s) within the group/discipline.</li><li>Lead and/or contribute to the implementation of large-scale initiatives and/or organizational changes (such as functional optimization) that affect the department.</li><li>Actively share knowledge with others across multiple disciplines and across lines through existing knowledge sharing processes and systems.</li></ul> Qualifications &amp; Experience Education and Experience:<ul><li>B.S. and/or M.S. in engineering, scientific or related field.&nbsp;</li><li>PMP and/or Six Sigma / Lean certifications are preferred.&nbsp;</li><li>Minimum 10+ years in biopharmaceutical/life-sciences industries is preferred.&nbsp;</li></ul>Required Competencies:&nbsp; Knowledge, Skills, and Abilities<ul><li>Proven experience in Operating Excellence, Project Management, and leading operations or continuous improvement teams.&nbsp;</li><li>Demonstrated leadership skills, including the ability to remove roadblocks, establish priorities, and maintain compliance sustainability.&nbsp;</li><li>Leadership experience and effective communication with stakeholders at all levels, along with a keen attention to detail.&nbsp;</li><li>Exceptional strategic thinking abilities, adept at managing complex systems, navigating organizational politics, fostering innovation, and skilled in negotiation and management.&nbsp;</li><li>Possesses a strategic perspective, leading with vision and values, exhibiting global acumen, and displaying a strong leadership disposition.&nbsp;</li><li>Strong customer focus, interpersonal and organizational skills, with a collaborative and teamwork-oriented mindset.&nbsp;</li><li>Proven ability to manage multiple tasks in a fast-paced environment.&nbsp;</li><li>Adept at working effectively across functional groups and teams to achieve objectives.&nbsp;</li><li>Demonstrated competencies in influencing, negotiating, relationship management, and a continuous improvement mindset.&nbsp;</li><li>Budget management experience, possesses an enterprise mindset, making decisions and sharing resources for the greater benefit.&nbsp;</li><li>Change agility, with the ability to navigate ambiguity, take calculated risks, and lead others through change.&nbsp;</li><li>Strong organizational and problem-solving abilities, with a sense of urgency and the capacity to manage priorities and timelines effectively.</li></ul>#HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Director RDQ Operations & Performance Management

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position SummaryReporting to the Senior Director, Executive and Strategic Communications, the Associate Director, Global Technical Services Communications, is responsible for developing and executing strategic communication initiatives that support Bristol Myers Squibb’s Global Technical Services operations. This role involves crafting high-quality written materials, providing strategic communication counsel, managing internal and external communications, and overseeing media relations and issues management.Global Technical Services (GTS) is part of BMS’ Global Product Development &amp; Supply (GPS) organization, and is responsible for enterprise-wide and business-critical technical capabilities, including Environmental Health, Safety &amp; Sustainability (EHSS), Global Sustainability, Capital Service and Solutions (CSS) and Global Engineering and Facilities (GEF).Key Responsibilities<ul><li>Implements internal and external communications strategies to elevate the company’s Global Technical Services function.</li><li>Maintains detailed knowledge and understanding of the company’s Global Technical Services operations, and observes relevant industry and business trends, to develop internal and external communication initiatives that advance the function’s strategic priorities.</li><li>Supports development and implements execution of organizational communications initiatives to promote employee engagement through town halls, employee communications across distinct working environments, internal videos, and other communication channels.</li><li>Manages Global Technical Services external communications initiatives to support BMS enterprise reputation through proactive media relations, digital and social media content; paid sponsorships, awards and rankings, events, speaking engagements and other strategically aligned initiatives.</li><li>Manages issues and special situations that may disrupt GPS operations and pose risk to enterprise reputation and stakeholder relationships.</li><li>Directs internal and external communication workstreams with agency partners in a collaborative manner.</li><li>Manages GPS communications related to the organization’s contributions to enterprise ESG commitments, including close collaboration with the BMS Purpose/ESG team and other key internal stakeholders.</li><li>Actively pursues and participates in professional development opportunities as part of a continual improvement culture.</li><li>Works collaboratively with colleagues to promote a high-performance culture that drives enterprise objectives, emphasizing accountability for results.</li></ul>Key Qualifications<ul><li>Approximately 7 to 10 years of communications experience in the pharmaceutical, life sciences or related industries is preferred, or a combination of professional experience that provides an equivalent career foundation in a large organization or agency setting.</li><li>Bachelor’s degree required, preferably in journalism, communications, public relations, or a related field.</li><li>Demonstrated fluency in ESG (Environmental, Social, and Governance) principles and communications, with the ability to effectively convey complex ESG concepts to diverse stakeholders.</li><li>Ability to interact effectively with colleagues at all levels of the company across a matrixed organization.</li><li>Ability to effectively counsel senior leaders.</li><li>Exceptional collaborative and team-building skills.</li><li>Exceptional writing, presentation, and interpersonal communication skills.</li><li>Strong research and analytical skills, with a keen attention to detail.</li><li>Ability to learn the business quickly and excel in a fast-paced, challenging environment.</li><li>Self-directed with proven ability to meet tight deadlines and balance multiple initiatives with competing priorities.</li><li>Proficiency with digital communications and effective use of social media platforms.</li><li>Understanding of ethical generative AI use in writing and content development.</li><li>Demonstrated ability to manage multiple workstreams, delegate effectively, and ensure appropriate visibility and information sharing occurs across matrixed organizations.</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Associate Director, GPS Communications, Global Technical Services and GPS Strategy

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position Summary: The Senior Manager, U.S. Label &amp; Launch Operations, Channel Operations is responsible for managing the operational processes associated with product labeling updates in the U.S. market. This role will define, drive, and execute the label updates across therapeutic areas to ensure compliance with prescribing information and is responsible for overseeing coherence across tactics of all brands.The role works closely with the Brand Teams, Commercial Regulatory Affairs, Worldwide Commercialization Excellence (WCE) and the cross-functional teams on strategy and execution of all label updates across various channels.The role will manage a team of contingent workers that are responsible for supporting channel operations (channel operation managers). The team will be responsible for the seamless implementation of updated labeling across all active brands.This is an important role within U.S. Commercialization Strategy &amp; Operations Organization and key to Bristol Myers Squibb’s ambition to continue advancing the efficient and expeditious execution of label update strategy and operations. In this position, this individual will report directly to the Associate Director, U.S. Label &amp; Launch Operations.Key Responsibilities:<ul><li>Track day-to-day multi-channel tactics from kick-off to delivery for label updates: Overseeing the execution of label updates across various channels, ensuring adherence to BMS standards.</li><li>Drive strategy and rollout of label updates: Collaborating with Commercial Regulatory Affairs Advisors to create and implement strategies for label updates.</li><li>Champion projects through medical, legal, regulatory review (PReP): Managing label update projects from prioritization to completion, ensuring smooth execution and compliance through the PReP process.</li><li>Create and refine accurate lists of tactics requiring label update: Identifying and managing all relevant tactics across channels for timely label updates.</li><li>Create presentations for key stakeholders: Communicating the strategy and status of operations to senior leadership and cross-functional teams.</li><li>Deliver on the accurate QC and approval of materials: Ensuring that all materials meet quality standards and are approved for production.</li><li>Identify, create, and implement efficiencies and innovations: Continuously improving processes to drive greater efficiencies and innovation within the Label &amp; Launch Operations</li><li>Lead label update communications: Proactively gathering and disseminating information to ensure timely and accurate communications.</li><li>Drive alignment meetings and status updates with agencies, third-party vendors, and stakeholders: Ensuring all parties are aligned and informed about the progress and updates for label-related projects.</li><li>Lead relationship-building with production agencies: Managing day-to-day operations with external partners to ensure smooth workflows and alignment with organizational needs.</li><li>Tightly manage all timelines and ensure creative assets are delivered to the production agency in the correct format and on time: Managing project timelines and ensuring the timely delivery of assets to third-party agencies.</li><li>Manage projects in Veeva Vault: Overseeing the management of label update projects within Veeva, developing systems to streamline workflow for active tactics.</li><li>Prepare strategy and communication decks: Creating decks to communicate strategy, progress, and key dates to stakeholders.</li><li>Actively monitor budgets for multi-channel tactics: Overseeing the financial aspects of label updates, ensuring proper budget tracking during annual, semi-annual, and day-to-day operations.</li><li>Closely manage the approval of estimates and Purchase Orders: Ensuring that all budget-related estimates and Statements of Work (SOWs) are accurately approved and monitored.</li><li>Define roles for Channel Operations Managers team members: Assigning tasks and responsibilities to ensure the effective distribution of workload within the team.</li><li>Create and provide training to Channel Operations Managers: Developing training programs to ensure team members are equipped with necessary knowledge to execute tasks efficiently.</li><li>Lead Label &amp; Launch Operations team in Associate Director’s absence: Acting as the leader for the team in the absence of the Associate Director, ensuring operations continue smoothly.</li><li>Develop subject matter expertise of brands and updates: Becoming the go-to expert on each brand and its updates to prescribing information, facilitating swift review and approval processes.</li><li>Manage master SharePoint Grid: Organizing and managing the master SharePoint Grid to track all relevant information for cross-functional teams.</li></ul>Qualifications &amp; Experience:<ul><li>Exemplary project management background.</li><li>Strong understanding of the key steps involved in the creation of print and digital tactics through multi-channel deployment.&nbsp;</li><li>Experience working in a multi-channel environment and ability to work in a matrix team setting</li><li>Ability to navigate complex and continually evolving organizational environments.</li><li>Excellent project and program management skills.</li><li>Strong written and verbal communication and presentation skills.</li><li>Ability to manage financial budgets for a large portfolio of various marketing tactics, including but not limited to estimates and invoices and ability to efficiently track multiple budgets.</li><li>Strong leadership skills and experience in managing teams through heavy workloads and competing deadlines.</li><li>Experience working with leadership and communicating directly with senior leaders.&nbsp;</li><li>Ability to learn new technology and systems quickly.</li><li>Multi-year experience working in project management systems specific to pharmaceutical companies.&nbsp;</li><li>Minimum level of education: Bachelor’s degree.</li><li>Pharmaceutical experience required </li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior Manager, U.S. Label & Launch Operations, Channel Operations

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Title:Associate Director, Program Management, Global Operations (Inline Asset Program Management)Location: Princeton Pike, NJ, Summit NJ, or Seattle, WAWithin the Cell Therapy Development and Operations (CTDO) division, the Portfolio Strategy and Operations (PSO) team focuses on the cell therapy pipeline as well as shaping product strategy throughout the lifecycle of a cell therapy asset. The organization encompasses the project managers, programs managers, portfolio management professionals and technical writing all of whom contribute to defining strategies for both early-and late-stage pipeline cell therapies enabling global regulatory approval and launches.&nbsp;The Associate Director, Program Management plays an important role in organizing, managing, and communicating the portfolio of projects aligned to the CTDO goals and objectives for specific asset/s, as well as providing project management skills and leadership for Inline products. This role will lead the execution of Global Operations (GO) brand team and management of the life cycle management (LCM) strategic portfolio and critical programs/projects. Assignments include operational responsibilities for governance and teams. Lead and direct complex, cross-functional, multi-site teams and workstreams, ensuring comprehensive planning and optimal execution of plans. Ensure interactions and timely collaboration with CTDO ecosystem, functional and site Project Management Offices (PMOs), key stakeholders and supporting functions. Proactively identify and facilitate risks, mitigations, resolution and escalation of issues, tracking and communicating status to stakeholders including leadership team.&nbsp; Leading program/projects and teams with passion, innovation, speed and accountability.The successful candidate will be a demonstrated leader with the breadth of professional experience and the drive to work with both internal and external partners to define and implement effective project management solutions. Key Responsibilities:<ul><li>Lead planning and execution of integrated, complex plans and teams for strategic CTO team programs &amp; projects, tech transfer governance, or GO team program management and other critical initiatives as defined by CTD/O management. Programs/Projects may include, but are not limited to, those identified during the annual book of work (BOW) prioritization and refresh process, strategic run-the-business initiatives, transformation, due diligence, business continuity, product launches, major change management, Quality &amp; Compliance, Operations, Product Development, Supply Chain, and significant regulatory activities.</li><li>Leads GO team operations including recurring status meetings, reporting, risk tracking, steering committee meetings, and conflict resolution, lead GO team BOW and ad hoc projects as necessary.</li><li>Develop and own execution plan for pre-launch, launch and post-launch activities aligned with asset/s strategy in partnership with the Product leader.</li><li>Coordinate across GO sub-teams to align, organize and provide direction aligned with strategy.</li><li>Prepare and manage governances until final decision and implementation.&nbsp; </li><li>Leads and guides BOW for asset/s across CTDO based on prioritization for respective GO team/s.</li><li>E2E operational management including budget, forecasting, performance against targets, facilitate key investment decision preparation / discussions in partnership with the Program leader. &nbsp;</li><li>Support preparation of business case/s for LCM strategic discussions (including strategy, operational plan, resource and budget component).</li><li>Develop and drive detailed plans, identifying critical path and timing while meeting strategic intent and achieving key milestones.</li><li>Ensure problem solving and decision making addressing major risks and issues by identifying, documenting, establishing mitigation plans, resolving, communicating or escalating to senior leadership when appropriate.</li><li>Collaborate with key stakeholders to manage expectations.&nbsp;</li><li>Drive consistency in project management tools and templates in line with CTDO PS&amp;O PMO best practices.</li><li>Plan/Execute change management strategy and plan.</li><li>Influence key stakeholders, develop project communications strategy, approach and plan.</li><li>Proactively drive scenario analyses to manage potential impact on plans and timelines and recommend strategic direction to management.</li><li>Foster diverse/inclusive high-performance teams and maintain strong relationships with operational and functional leadership.</li><li>GO team program management responsibilities (in addition to major responsibilities above): </li><li>Develop and provide performance oversight and reporting of GO Team goals and objectives.</li><li>Establish the approved brand project portfolio, working with sponsors to define scope and deliverables, define project team and project management resource requirements and work within the PMO ecosystem to identify project managers, coaching and mentoring less experienced PMs when needed.</li><li>Provide disciplined project prioritization and oversight to the GO Team BOW as defined by the SPL, GO Team and related sub-teams.</li><li>Manage the GO Team project portfolio and “change-space.”&nbsp; Support development, approval, execution and reporting of portfolio projects.</li><li>Provide program-level leadership and direction to project managers.&nbsp; Coordinate interactions, ensure timely and optimal execution of projects, and effectively collaborate with key stakeholders.</li><li>Provide project management expertise for GO Team/s operations, e.g., meeting scheduling, agendas, minutes, etc.</li><li>Support product life cycle strategy management, including due diligence, alliance management, launch planning and execution, and technology transfer.&nbsp; </li><li>Guide &amp; influence Integrated Development, GO and Market Launch Teams in creating robust life cycle management plans.</li><li>Work with key GO Team members to ensure continuity of supply, end-to-end optimization, comprehensive change management, and effective management of technology and regulatory issues.&nbsp; </li></ul>Qualifications &amp; Experience:<ul><li>B.S. in Engineering, Pharmacy, science or technical discipline, advanced degree preferred.</li><li>PMP certification highly desirable.</li><li>Understanding of cGMPs and regulatory CMC.</li><li>A minimum of 10 years in BioPharma operational or development discipline, including demonstrated experience managing complex projects.</li><li>Experience in project/program management of complex projects involving cross-functional, multi-site, international teams.</li><li>Experience with manufacturing sites and staff.</li><li>Proficiency with project management and Microsoft tools e.g. Project, Excel, PowerPoint, SharePoint.</li></ul><ul><li>Ability to achieve results and exercise influence across a global matrix organization (e.g., operations, manufacturing technology, quality, supply chain, finance, R&amp;D). </li><li>Ability to work independently with high level of accountability.</li><li>Excellent verbal, written and presentation skills and have the ability to deal effectively with all levels of management. </li><li>Strong analytical skills, well organized and capable of managing multiple projects with respect to priorities. </li><li>Ability to exercise discretion, discernment and to be comfortable to operate when erroneous decisions will have serious impact on the overall success of operations.</li></ul><ul><li>Ability to interact internally and externally with executive level management, requiring negotiation of potentially difficult and sensitive matters to influence policy making bodies both internally and externally.</li><li>Familiarity with financial principles, core business concepts, and business and operations management. </li><li>Ability to develop business analysis and reporting.</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.The starting compensation for this job is a range from $156,000 - $195,000 (if based in NJ) and $166,000 - $208,000 (if based in WA), plus incentive cash and stock&nbsp;opportunities (based on eligibility).&nbsp; The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided based on demonstrated experience.&nbsp;Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS&nbsp; Career Site.&nbsp; Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical,&nbsp;pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP).&nbsp;Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental&nbsp;health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays,&nbsp;Global Shutdown days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick&nbsp;time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and&nbsp;surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like&nbsp;tuition reimbursement and a recognition program.&nbsp;#LI-HybridBMSCARTVETERANIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Associate Director, Program Management, Global Operations (Inline Asset Program Management)

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position SummaryThe Director Global Policy and Business Strategy Integration is responsible for developing and implementing a Global Policy Strategy aligned with the business priorities with direct accountability for Oncology and Hematology TAs, and overall corporate goals.This role is accountable to ensure that Policy &amp; Government Affairs insights are fully integrated into commercial business planning to support the success of BMS’s product portfolio and commercial strategy and will participate as a member of the Worldwide Oncology and Hematology TAs leadership team.The Director will work in partnership with the prioritized markets to advance key policy initiatives aligned with the Global Policy Strategy.This position requires strong leadership skills, matrix influence, and provide guidance to senior leadership. Key Responsibilities Global Policy and Business Strategy Coordination:Leadership in Strategic Alignment: Lead efforts to ensure that global policy strategies are synchronized with commercial priorities and enterprise goals, driving the success of the Oncology and Hematology TAs.Joint Objective Setting: Effectively collaborate with cross-functional teams, including commercial, market access, medical, and R&amp;D, to set and execute joint objectives, linking policy initiatives to therapeutic and product goals.Policy Integration into Business Planning:Strategic Integration: Ensure that Policy &amp; Government Affairs insights are integrated into the business planning processes for the Oncology and Hematology TAs, and the broader enterprise strategy.Cross-Functional Engagement: Collaborate across functions such as commercial, market access, medical, and R&amp;D to ensure that policy insights are factored into product launch plans, market access, lifecycle management and portfolio prioritization strategies.Market and Therapeutic Area Support:Direct Market Support: Offer hands-on guidance and strategic support to key markets on high-priority projects designed to drive Oncology and Hematology TAs strategic objectives, adapting global strategies to local needs.Therapeutic Area Focus: Ensure policy strategies are adapted to address the specific challenges and opportunities of Oncology and Hematology TAs, such as access, regulatory approvals, and reimbursement frameworks.Leadership and Matrix Influence:Matrix Leadership: Lead and influence across a complex global matrix organization, ensuring Global Policy strategy alignment with business priorities.Executive Presence: Represent the GPIGA function within senior leadership settings, including the Worldwide Oncology and Hematology TAs, leadership team.Policy Advocacy and External Engagement:Advocacy Leadership: Develop and implement Policy Advocacy initiatives by engaging with external stakeholders, including government bodies, regulatory agencies, and industry organizations, to support policy outcomes that advance business goals.Stakeholder Engagement: Foster long-term external multistakeholder relationships to shape favorable policy environments for Oncology and Hematology TAs.Performance Monitoring and Reporting:Impact Monitoring: Develop and establish systems to track and evaluate the impact of policy initiatives on Oncology and Hematology TAs and business outcomes, with regular reporting to senior leadership.KPIs and Metrics: Define and monitor key performance indicators (KPIs) to measure the effectiveness of global policy strategies in advancing business outcomes. Qualifications &amp; Experience Education:Advanced degree in business, public policy, political science, law, or a related field. MBA or JD preferred.Experience10 years of experience in public policy, government affairs, marketing, market access, strategy, or a related field, with significant experience in the pharmaceutical or healthcare industry.Proven track record of organizational leadership and management experience, the ability to motivate others to advance goals, and the ability to effectively manage multiple projects or roles in a rapidly evolving environment.Proven track record of influential leadershipIn-depth understanding of the pharmaceutical industry, therapeutic area dynamics, and business strategy.Skills:Communication Skills: Excellent communication skills and executive presence to engage with senior leaders.Consensus building: Demonstrated skills in leading consensus-building processesLeadership and Influence: Strong leadership skills with the ability to drive coordination in a matrixed environment across diverse global teams and Global-to-markets and ability to lead and influence senior-level policy discussions both internally and externally.Global Perspective: ability to navigate in&nbsp; complex global regulatory, policy and business environments.Strategic Thinking: Understands the long-term business strategy and related internal and external challenges while creating operational plans that help execute the longer-range plan. Ability to coordinate policy efforts with broader business strategies to achieve long-term goalsRole based in NJ Travel as required#LI-HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Director, Global Policy and Business Strategy Integration – Oncology and Hematology Therapeutic Areas

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position SummaryThe Director Global Policy and Business Strategy Integration is responsible for developing and implementing a Global Policy Strategy aligned with the business priorities with direct accountability for Immunology, Cardiovascular and Neuroscience TAs, and overall corporate goals.This role is accountable to ensure that Policy &amp; Government Affairs insights are fully integrated into commercial business planning to support the success of BMS’s product portfolio and commercial strategy and will participate as a member of the Worldwide Immunology, Cardiovascular and Neuroscience TAs leadership team.The Director will work in partnership with the prioritized markets to advance key policy initiatives aligned with the Global Policy Strategy.This position requires strong leadership skills, matrix influence, and provide guidance to senior leadership. Key Responsibilities Global Policy and Business Strategy Coordination:Leadership in Strategic Alignment: Lead efforts to ensure that global policy strategies are synchronized with commercial priorities and enterprise goals, driving the success of the Immunology, Cardiovascular and Neuroscience TAs.Joint Objective Setting: Effectively collaborate with cross-functional teams, including commercial, market access, medical, and R&amp;D, to set and execute joint objectives, linking policy initiatives to therapeutic and product goals.Policy Integration into Business Planning:Strategic Integration: Ensure that Policy &amp; Government Affairs insights are integrated into the business planning processes for the Immunology, Cardiovascular and Neuroscience TAs, and the broader enterprise strategy.Cross-Functional Engagement: Collaborate across functions such as commercial, market access, medical, and R&amp;D to ensure that policy insights are factored into product launch plans, market access, lifecycle management and portfolio prioritization strategies.Market and Therapeutic Area Support:Direct Market Support: Offer hands-on guidance and strategic support to key markets on high-priority projects designed to drive Immunology, Cardiovascular and Neuroscience TAs strategic objectives, adapting global strategies to local needs.Therapeutic Area Focus: Ensure policy strategies are adapted to address the specific challenges and opportunities of Immunology, Cardiovascular and Neuroscience TAs, such as access, regulatory approvals, and reimbursement frameworks.Leadership and Matrix Influence:Matrix Leadership: Lead and influence across a complex global matrix organization, ensuring Global Policy strategy alignment with business priorities.Executive Presence: Represent the GPIGA function within senior leadership settings, including the Worldwide Immunology, Cardiovascular and Neuroscience TAs, leadership team.Policy Advocacy and External Engagement:Advocacy Leadership: Develop and implement Policy Advocacy initiatives by engaging with external stakeholders, including government bodies, regulatory agencies, and industry organizations, to support policy outcomes that advance business goals.Stakeholder Engagement: Foster long-term external multistakeholder relationships to shape favorable policy environments for Immunology, Cardiovascular and Neuroscience TAs.Performance Monitoring and Reporting:Impact Monitoring: Develop and establish systems to track and evaluate the impact of policy initiatives on Immunology, Cardiovascular and Neuroscience TAs and business outcomes, with regular reporting to senior leadership.KPIs and Metrics: Define and monitor key performance indicators (KPIs) to measure the effectiveness of global policy strategies in advancing business outcomes. Qualifications &amp; Experience Education:Advanced degree in business, public policy, political science, law, or a related field. MBA or JD preferred.Experience10 years of experience in public policy, government affairs, marketing, market access, strategy, or a related field, with significant experience in the pharmaceutical or healthcare industry.Proven track record of organizational leadership and management experience, the ability to motivate others to advance goals, and the ability to effectively manage multiple projects or roles in a rapidly evolving environment.Proven track record of influential leadershipIn-depth understanding of the pharmaceutical industry, therapeutic area dynamics, and business strategy.Skills:Communication Skills: Excellent communication skills and executive presence to engage with senior leaders.Consensus building: Demonstrated skills in leading consensus-building processesLeadership and Influence: Strong leadership skills with the ability to drive coordination in a matrixed environment across diverse global teams and Global-to-markets and ability to lead and influence senior-level policy discussions both internally and externally.Global Perspective: ability to navigate in&nbsp; complex global regulatory, policy and business environments.Strategic Thinking: Understands the long-term business strategy and related internal and external challenges while creating operational plans that help execute the longer-range plan. Ability to coordinate policy efforts with broader business strategies to achieve long-term goalsRole based in NJ Travel as required#LI-HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Director, Global Policy and Business Strategy Integration – Immunology, Cardiovascular and Neuroscience Therapeutic Areas

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Our BMS pipeline is a core catalyst for achieving sustained growth through 2030 and will benefit millions of patients with cancer and other serious diseases.&nbsp; To deliver this promise, we require an R&amp;D operating model that is efficient, resilient, and flexible in the face of a rapidly evolving external and internal landscape.&nbsp; Our R&amp;D Strategy Implementation &amp; Operational Excellence team is comprised of industry and strategic change execution experts who will navigate and guide the R&amp;D organization through our journey and transformation.&nbsp; We provide members of our team the opportunity to work on high priority, challenging, and personally fulfilling strategic initiatives.Position SummarySupport the development and execution of Drug Development’s (DD) Innovation strategy in partnership with DD Leaders, Process Council, and Business Insights &amp; Technology (BIT) partners.&nbsp; This role will support our DD business in translating business needs into an overall set of priority imperatives and executing initiatives to deliver meaningful cycle time, quality, and cost benefits.&nbsp; The role will require experience with Innovation, emerging technologies, product development / roadmaps, transformational / change leadership, and executive facilitation.&nbsp; Our team works across a variety of key partners in a highly matrixed organization and, therefore, must excel in cross-functional collaboration, stakeholder management, an influencing without authority.Key ResponsibilitiesInnovation Initiative Strategy Execution: Drives the lifecycle of an innovation project which includes scoping, goal setting, solution designing, implementation, full realization, and close-out for the most impactful cross-functional initiatives.&nbsp; Project chartering, team mobilization, project planning, risk/issue management, change planning, and communications are all part of the day-to-day responsibilities.Innovation Program Governance and Portfolio Management: Will provide support to the Innovation Program Sponsor and Innovation Strategy Implementation Lead in governance committee and portfolio management operations.&nbsp; This may entail agenda setting, preparations, facilitation, and close-out of governance meetings.&nbsp; This also entails providing the necessary project details and presentations to support portfolio and project-level reviews.Innovation Adoption: Manage work streams or tactics within our overarching Innovation Adoption strategy to elevate the DD org’s overall understanding, receptivity, and adoption of new and innovative ways of working.&nbsp; These are broader scale change and learning tactics above the learning tactics developed for specific projects.Innovation Strategy Formulation: Will support the Innovation Program Sponsor and Innovation Strategy Implementation Lead in the development of an overarching Innovation strategy.&nbsp; Specific assignments/tasks may include synthesizing business leader perspectives and translating into key requirements or imperatives, aligning priorities across functions and stakeholder groups, establishing measurable goal/outcome statements for our priorities, and partnering with our BIT and DD SMEs colleagues to develop solution blueprints and business cases endorsed by DD leaders.Innovation External Partnerships: In coordination with DD and enabling function partners (BIT, BD, Procurement), may participate in external scans/sourcing for external innovation and partnerships to advance our business imperatives (as needed).Qualifications &amp; ExperienceBS/BA Degree in Business Management or related field required; advanced degree in&nbsp;related discipline preferred (e.g., Degree in Life Sciences&nbsp;(MBA, MS, PhD, Pharm D).7+ years of combined experience in all or majority of the following areas: <ul><li>Innovation management, digital strategy development and product development / management</li><li>Pharma R&amp;D experience, preferably Clin Dev’t, Trial Operations, Biostatistics, Regulatory, Safety, etc</li><li>Transformational change leadership (certifications a plus but not required)</li><li>Operational excellence and/or process improvement (certifications a plus but not required)</li></ul>Excellent communication and interpersonal skills, with the&nbsp;ability to interface with a broad range of internal and external&nbsp;stakeholders at all levels of the&nbsp;organization. &nbsp;​ This includes the ability to listen, understand requirements, and convey information clearly and concisely. Ability to lead and motivate teams, facilitate discussions, and influence stakeholders to drive initiatives. This includes the ability to inspire and empower others, resolve conflicts, and foster a culture of continuous improvement.High proficiency in and demonstration of critical thinking,&nbsp;problem-solving, and decision&nbsp;making.Anticipates needs and assesses and manages business and&nbsp;organizational&nbsp;risks.Demonstrated innovation, flexibility, open-mindedness, and&nbsp;adaptability to meet objectives in a rapidly changing&nbsp;environment with shifting&nbsp;priorities.Has proven track record on delivering resultsIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

36 Procurement / Operations Jobs in New Jersey