Celgene International SaRL Posted September 11, 2026

Senior Scientist

Boudry, Switzerland Full time
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Celgene International SaRL is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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  adastaffingsupport@bms.com . 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/

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  TAEnablement@bms.com 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.

R1606196 : Senior Scientist

Job details

Seniority
Senior
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Boudry, Switzerland
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 508 comparable Senior Manufacturing & CMC roles across 69 biopharma companies.

508Comparable roles tracked
446Currently active
69Companies hiring similar roles
29Countries represented

Salary context

198 of 508 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Sr Manufacturing Technician · Genz. Therap Product LP $2,400/yr – $3,200/yr
Highest disclosed · Associate Director / Director, CMC Product Development · AbbVie $160,500/yr – $305,000/yr
Peer group range $2,800 – $232,750 (median $146,150)

Where these roles are based

Top locations among the 508 comparable roles

United States323
India45
Ireland15
Netherlands15
Singapore11
China's Mainland10

+ 23 more countries

Seniority mix

508 of 508 peers have a known seniority level

Senior319
Principal99
Associate Director90

Therapeutic area mix

0 of 508 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Roche Rotkreuz, Zug, Switzerland Senior
Same function Same seniority Same country
60%similar
Roche Rotkreuz, Zug, Switzerland Senior
Same function Same seniority Same country
60%similar
Roche Basel, Basel-City, Switzerland Senior
Same function Same seniority Same country
60%similar
Roche Basel, Basel-City, Switzerland Senior
Same function Same seniority Same country
60%similar
Incyte Yverdon-les-Bains, Switzerland Senior
Same function Same seniority Same country
60%similar
Roche Basel, Basel-City, Switzerland Senior
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Senior Project Lead MSAT
Roche · Rotkreuz, Zug, Switzerland · Senior
Function Therapeutic area Seniority Country
60%
MSAT Senior Process Expert USP
Roche · Basel, Basel-City, Switzerland · Senior
Function Therapeutic area Seniority Country
50%
Senior/Principal Associate in Pharmaceutical Technical Development – Drug Product Formulation & Process Development - fixed term for 2 years
Roche · Basel, Basel-City, Switzerland · Principal
Function Therapeutic area Adjacent seniority Country
45%
Senior Associate Proteins Bioanalytics with Mass Spectrometry Expertise (m/f/d
Roche · Penzberg, Bavaria, Germany · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.