Sobre este puesto de Senior Scientist en Bristol Myers Squibb
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.
MS&T is a science-driven organization dedicated to building deep scientific and technical knowledge of our products and processes across the full pharmaceutical lifecycle. The organization supports both internal and external manufacturing and packaging networks, ensuring robust, compliant, and efficient supply.
The Senior Scientist, Drug Product & Packaging is an experienced individual contributor who provides strong scientific and technical expertise in support of drug product and packaging processes for commercial and late-stage products. The role focuses on execution, problem solving, and technical depth within defined project scopes and operates with a high degree of autonomy while aligning with strategies and priorities set by senior MS&T leadership.
The Senior Scientist is expected to independently handle complex technical assignments, contribute significantly to cross-functional teams, and apply sound scientific judgment to support reliable product supply, compliance, and continuous improvement.
Duties/Responsibilities
- Serve as a subject matter contributor for drug product and packaging processes
- Contribute to standards and SOPs
- Support investigations and root cause analysis
- Contribute to CQAs, CPPs, and control strategies
- Design and execute technical and validation studies
- Technology Transfer & Lifecycle Management
- Support DP and packaging tech transfer
- Ensure knowledge capture via TPT
- Support lifecycle improvements
- Project & Documentation Responsibilities
- Own defined technical workstreams
- Author and review GMP documentation
- Support CMC submissions
- Scientific Excellence & Continuous Improvement
- Maintain scientific expertise
- Drive continuous improvement
Qualifications
Specific Knowledge, Skills, Abilities:
- Good working knowledge of QA, cGMP, and the Pharmaceutical Regulatory framework.
- Good knowledge of various types of pharmaceutical packaging processes/technologies.
- Good knowledge of Technology Transfer and validation.
- Working knowledge Lean and 6 Sigma methodologies.
- Good leadership skills and ability to influence and work across organizational boundaries.
- Effective communication skills, good command of English and preferably another European language.
Education/Experience/ Licenses/Certifications:
- Minimum bachelor’s degree in Process/Packaging Engineering/Technology, Process/Packaging Development, or similar education in this field.
- 5-8 years of experience in the Pharmaceutical/Cosmetics/Food industry.
- Experience in the development/application design and their implementation.
- Knowledge and experience of pharmaceutical packaging materials.
- Demonstrated project leadership. Experience of multi-site/cross-site project management.
We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.
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 [email protected]. 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/
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If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with 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.
