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Vice President, General Manager & Campus Lead, Devens


Job Location:

Devens, MA - USA

Yearly Salary: USD 330690 - 400722
Posted: 1 October 2026 (10 hours ago)
Application Deadline: 29 December 2026
Vacancies: 1 Vacancy

Job Summary

At Bristol Myers Squibb our employees often ask Who are you working fora question that fuels collaboration accountability and urgency in our work. Our purpose-driven culture inspires us to discover develop and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work opportunities for growth and a supportive environment that values inclusion wellbeing flexibility and comprehensive benefits. This is work that transforms the lives of patients and the careers of those who do it.




Position Summary

The General Manager Devens is the senior leader accountable for the end-to-end performance compliance and strategic direction of BMSs large-scale commercial biologics Global Business Unit (GBU) operations at Devens and serves as the Campus Lead for the full Devens site spanning both the GBU Biologics organization and the Cell Therapy business unit.

This role oversees all GBU Biologics site operations at Devens from cell culture and manufacturing sciences & technology (MS&T) to large-scale commercial drug substance production with full accountability for talent development safety quality regulatory compliance supply reliability and cost management across the Biologics organization.

As Campus Lead the General Manager also owns end-to-end site services and shared infrastructure Site Engineering Environmental Health & Safety Security and Facilities that support both the GBU Biologics and Cell Therapy business units operating on the Devens campus ensuring both organizations have the capacity capabilities and infrastructure to deliver on their respective missions.

A defining focus of this role over the next several years is leading the transformation and integration of the GBU Biologics and Cell Therapy business units at Devens building a single unified campus operating model governance structure and culture that harmonizes site services talent and ways of working across both modalities. This includes championing innovative digitally enabled and AI-driven transformation advanced analytics automation digital twins and other Industry 4.0 capabilities to reimagine site processes accelerate integration and establish Devens as a smart campus that delivers sustainable competitive advantage.

The General Manager also serves as the primary representative of the Devens campus both within the global manufacturing network (driving adoption of world-class standards and sharing best practices across BMSs network of manufacturing sites) and externally (engaging with regulatory authorities government officials industry partners and the local community to uphold the Companys reputation and advance strategic initiatives).

This position is pivotal in ensuring that the Devens campus remains a world-class innovative biologics and cell therapy manufacturing hub that reliably delivers life-saving medicines to patients while successfully transforming into a single integrated future-ready campus.

Key Responsibilities

In this role the General Manager will provide strategic technical and operational leadership across a broad range of functional domains and both business units at Devens. Key responsibilities include:

  • Strategic & Enterprise Leadership: Develop and execute Devens long-range strategy in alignment with BMSs global manufacturing network GBU pipeline plans and Cell Therapy growth objectives. Ensure the sites capabilities evolve in step with enterprise needs including readiness for new biologics modalities and Cell Therapy platform expansion. Represent Devens in Product Development and Supply (PDS) and Cell Therapy governance forums and in enterprise-wide manufacturing network forums (e.g. Factory Level Optimized Work (FLOW) best practice standardization). Anticipate industry trends and build site-level strategies and contingency plans that maintain a competitive edge for both business units.
  • Biologics Manufacturing Operations & Technical Excellence: Oversee all GBU Biologics drug substance manufacturing operations at Devens ensuring reliable supply of high-quality biologics to meet commercial demand and clinical pipeline needs. Maintain rigorous standards for safety quality and efficiency across cell culture purification and manufacturing sciences & technology (MS&T) operations. Drive effective technology transfer and scale-up of new processes enabling rapid industrialization of new biologic therapies while minimizing risk and optimizing time-to-market.
  • Campus Leadership & Cross-Business Unit Governance: Serve as the Campus Lead for the full Devens site with end-to-end accountability for shared infrastructure and services Site Engineering EHS Security and Facilities that enable both the GBU Biologics and Cell Therapy business units to operate safely reliably and efficiently. Establish and chair a unified campus governance model and leadership forum that brings GBU Biologics and Cell Therapy leadership together to align priorities resolve cross-business unit resource and capacity trade-offs and represent one Devens voice to the enterprise.
  • Site Transformation & Business Unit Integration: Lead the multi-year transformation and integration of the GBU Biologics and Cell Therapy business units at Devens into a single unified campus operating model. Design and execute the integration roadmap covering organizational structure ways of working shared services talent and culture in close partnership with GBU and Cell Therapy senior leadership. Serve as the primary change agent for the transformation building momentum managing risk and ensuring business continuity for both business units throughout the integration period.
  • Quality EHS & Regulatory Compliance: Champion a world-class safety and quality culture across the full Devens campus. Ensure full compliance with global GMP standards EHS regulations and all regulatory requirements across biologics and cell therapy manufacturing processes. Serve as the sites executive sponsor during regulatory inspections and audits maintaining a state of constant inspection readiness. Model and enforce behaviors that prioritize patient safety product quality and a safe working environment aiming for zero safety incidents and the highest levels of regulatory confidence.
  • Digital Transformation & AI-Driven Innovation: Lead Devens journey toward becoming a smart digitally enabled campus. Drive the adoption of AI/ML predictive analytics automation robotics and other Industry 4.0 technologies to improve manufacturing efficiency agility and reliability and to accelerate the sites transformation and integration agenda. Champion AI and advanced analytics for predictive maintenance yield optimization and proactive deviation management. Partner with BMS Digital and IT teams to pilot and scale enterprise digital initiatives ensuring the workforce is trained and adaptable to new digital tools.
  • Capital Projects & Operational Excellence: Spearhead the planning and execution of major capital projects and technical upgrades at the Devens campus integrating modular facility design single-use technologies and automation to increase flexibility and throughput for both business units. Oversee operational readiness for new facilities and equipment from commissioning to validation and ramp-up. Continuously improve operational processes through a Lean and Six Sigma approach driving productivity improvements cost reduction and waste elimination while protecting product quality and supply consistency.
  • Talent & People Leadership: Foster a high-performance inclusive culture that attracts develops and retains top talent across both business units. Lead and mentor the sites multi-disciplinary leadership team ensuring all functional areas work toward common goals. Build a future-ready workforce with strong technical expertise in biologics and/or cell therapy and digital proficiency. Act as a role model for BMSs values and leadership behaviors promoting cross-functional collaboration and a culture of innovation especially through the integration period.
  • Financial & Business Accountability: Manage the sites P&L and financial performance for GBU Biologics operations and oversee the shared campus services budget supporting both business units. Develop and oversee annual operating budgets and long-range financial plans setting ambitious yet achievable targets. Rigorously track the return on investment (ROI) for capital projects digital innovations and integration initiatives ensuring robust financial controls and forecasting.
  • External Engagement & Stakeholder Management: Serve as the key liaison between the Devens campus and external stakeholders including government officials regulatory agencies industry associations and the local community. Proactively engage with health authorities to build trust and ensure open communication. Champion BMSs reputation in the community by supporting corporate social responsibility initiatives and upholding high standards of environmental stewardship and ethical operation.


Qualifications & Experience

  • Education: Bachelors degree in Engineering Life Sciences Pharmacy Biochemistry or a related field is required. An advanced degree (M.S. Ph.D. or MBA) is strongly preferred especially with specialization in biotechnology pharmaceutical sciences or business management.
  • Experience: Approximately 15 years of progressive experience in pharmaceutical/biopharmaceutical manufacturing with significant leadership in large-scale biologics drug substance operations. Experience introducing and scaling up new modalities from late-stage development into full commercial production is highly desirable; experience with cell therapy or other advanced/complex therapy manufacturing is a strong plus. A track record of leading large-scale organizational transformations or business unit integrations (e.g. site consolidations combining business units network integrations) is required.
  • Technical & Compliance Knowledge: Deep knowledge of Good Manufacturing Practices (GMP) and regulatory requirements (e.g. FDA EMA and other global health authorities) is essential as is familiarity with EHS regulations and best practices for biologics and cell therapy manufacturing environments. Proven experience hosting or leading regulatory inspections and interacting with regulatory agencies is expected. Experience with large capital project planning and execution including facility expansions or introduction of new production lines is required as well as strong understanding of financial management processes and P&L responsibility for a manufacturing site or business unit.
  • Digital & AI-Driven Transformation: Demonstrated expertise leading innovative digitally and AI-driven transformations including AI/ML implementation in manufacturing operations digital twins and/or simulation technologies predictive analytics automation and robotics. A proven ability to reimagine ways of working through emerging technology and to build the organizational capability needed to sustain a digitally enabled site.
  • Leadership: Demonstrated ability to lead cross-functional multicultural teams and develop well-integrated high-performing organizations across multiple business units. Excellent leadership qualities are needed including strategic thinking results-driven decision making and the ability to influence across executive levels and functions. Exceptional communication skills and stakeholder management capabilities (including engagement with external partners government officials and regulatory bodies) are critical. The ideal candidate will have experience managing multi-site or large complex sites and a strong grasp of the legal cultural and organizational nuances of leading in a global matrixed environment. The role demands a leader who exemplifies a true enterprise mindset prioritizing the success of the broader campus business units and BMS network above any single function with high accountability for performance scientific and technical curiosity a passion for innovation and digital advancement and the ability to inspire and transform organizational culture through complex multi-year change.
  • Enterprise Mindset & Change Leadership: Proven track record leading complex multi-year organizational transformations and business unit integrations with the judgment to sequence change manage ambiguity and sustain safety quality and supply performance through disruption. Skilled at building unified governance and culture across previously separate organizations aligning stakeholders around a shared campus vision and balancing enterprise priorities against individual business unit needs.

We hire for skills and capabilities not just credentials if this role excites you but doesnt perfectly match your resume we encourage you to apply anyway.

Compensation Overview:

$330690 - $400722

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully carefully considering the nature of the role required skills work location schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors and individual team or Company performance.


Benefits:


Subject to the terms and conditions of the applicable plans then in effect you may be eligible to participate in our comprehensive benefit plans including wellbeing support retirement and financial protection benefits and insurance offerings (medical dental vision life and disability).


U.S.-based exempt employees are eligible for Flexible Time Off (FTO) which provides paid time off without a set accrual limit subject to manager approval along with 11 paid company holidays each year.


Non-exempt employees RayzeBio employees and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval) 11 paid company holidays and 3 optional holidays.


Depending on eligibility employees may also have access to additional time-off benefits including paid sick leave up to two paid volunteer days per year summer hours flexibility and leaves of absence for medical personal parental caregiver bereavement or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Years Day.


U.S.-based job seekers can explore full benefit offerings at We Work

Where you work matters because collaboration innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential site-by-design field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application or in any part of the recruitment process direct your inquiries to. Visit access our complete Equal Employment Opportunity statement.


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Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more

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