Associate Director: Process Technology Transfer

Bristol Myers Squibb; Harvard (MA); On-site; USD 178,000 - 216,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Comprehensive benefits

Job summary

Bristol Myers Squibb seeks an Associate Director to lead technology transfer and optimize process efficiency at the Devens MA facility. You will oversee multi-disciplinary teams, drive product introductions, and coordinate resources to meet production targets for clinical and commercial products.

Key responsibilities include overseeing changeover, continuous improvement, and manufacturing scheduling while championing safety and regulatory compliance.

Qualifications

• 10+ years in biopharmaceutical manufacturing or equivalent.
• Mastery of SOPs and cGMPs within a regulatory environment.
• Strong leadership and change management capabilities.

Responsibilities

• Leads technology transfer and new product introduction into the manufacturing facility.
• Directs changeover, continuous improvement initiatives, and production scheduling.
• Allocates resources for deviations, defects, and changes to maintain safe production.
• Builds high-performing teams and fosters continuous learning and innovation.
• Maintains performance metrics and drives cost, quality, safety, and service goals.
• Supports health authority inspections and cross-functional collaboration.

Skills

Leadership

Process transfer

Cross-functional collaboration

Regulatory compliance

Project management

Manufacturing automation

Education

Ph.D. in biological sciences / chemical engineering

M.S. in relevant discipline

B.S. in related field

Tools

Process control systems

Job description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a 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.

PRINCIPAL OBJECTIVE OF THE POSITION

Lead and develop multifunctional teams to ensure effective process technology transfer of commercial and clinical products manufactured at the Devens Single Use Facility, resolve process issues, and optimize process and facility efficiency. This role is accountable for maximizing productivity, minimizing costs, and resolving process challenges through leadership, technical expertise, and cross-functional resource coordination.

Major Duties And Responsibilities

• Leads technology transfer and new product introduction into the manufacturing facility. Accountable for providing support to manufacturing teams to achieve production targets for clinical and commercial products.
• Directs activities associated with product changeover, continuous improvement initiatives, project prioritization, and production and maintenance scheduling to meet site metrics.
• Allocates department resources to support deviations, defects, and changes associated with maintaining safe and compliant production.
• Champions the company's, site's, and department's mission, goals, and guidelines, taking action that advances cultural evolution, innovation, and leadership across the organization.
• Promotes and demonstrates safety leadership in pursuit of an injury-free operating environment, ensuring safety investigations and CAPAs are closed promptly.
• Collaborates with Manufacturing staff to identify trends, variances, and bottlenecks in the manufacturing process, and helps develop solutions to maximize productivity, quality, and process efficiency.
• Recruits and develops a high-performing team with diverse backgrounds and talents; coaches and counsels team members to build their skills and fosters an environment of continuous learning, improvement, and innovation.
• Maintains and communicates performance metrics to the team, setting and upholding high performance expectations.
• Establishes an environment that fosters continuous improvement in cost, quality, safety, and customer service.
• Builds and maintains strong relationships inside and outside the organization.
• Supports health authority inspections.

Knowledge And Skills

• B.S. in biological sciences, chemical/biochemical engineering, or a related discipline, with a minimum of 10 years of relevant experience in the biopharmaceutical industry, or equivalent experience; or
• M.S. in the same disciplines, with a minimum of 6 years of relevant experience in the biopharmaceutical industry, or equivalent experience; or
• Ph.D. in biological sciences, chemical/biochemical engineering, or related discipline.
• Mastery of SOPs and cGMPs, with the know-how to work and manage within a regulatory environment.
• Demonstrated aptitude for engineering principles and manufacturing automation systems.
• Demonstrated ability to shift the thinking of, or gain acceptance from, others in sensitive situations.
• Proven leadership ability to make difficult decisions in a logical, rational manner; demonstrated ability to work as a senior management team member and engage and influence team members in a matrixed environment.
• Previous managerial experience demonstrating proficiency in selecting, motivating, and retaining a high-performing team; effectively managing personnel issues; and planning and administering financial resources.
• Adaptable to a fast-paced, complex, and ever-changing business environment.
• Effective communication skills to coordinate with support groups and obtain needed cooperation and support in a timely and effective manner.
• Demonstrated strong track record of change management, including implementation of continuous improvement and OPEX strategies.

Compensation Overview

Devens - MA - US: $178,420 - $216,197

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 Year's Day.

U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

How 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 https://careers.bms.com/ways-of-working.

Supporting People With Disabilities

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 [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: 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: https://careers.bms.com/california-residents/

For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1607685 : Associate Director: Process Technology Transfer