Scientist Stability (m/f/d) – Hybrid Role

Stability testing, Drug Substance/Product, 7-Months contract

Exciting Opportunity in a Global Pharmaceutical Environment
For our client, a leading international biopharmaceutical company, we are currently looking for a motivated and experienced Scientist Stability to join the Global Biopharmaceutical Stability team.

In this role, you will be responsible for stability strategies and oversight of commercial Drug Substance and Drug Product stability programs within a highly collaborative global environment.

Your Responsibilities

• Act as Stability Product Lead for assigned commercial products
• Develop and oversee stability strategies and stability programs
• Author, review, and approve stability protocols and reports
• Support regulatory submissions including CTD dossiers, annual reports, and product renewals
• Participate in product transfers and perform gap assessments against global requirements
• Support Change Controls, CAPAs, OOT/OOS investigations, and quality-related activities
• Coordinate annual commercial stability programs with sample management teams
• Collaborate with cross-functional international teams and external partners
• Support health authority inspections and audits
• Contribute to Operational Excellence initiatives to improve and standardize stability processes

Your Profile

• Bachelor’s degree in Chemistry, Biology, Microbiology, or a related scientific discipline
• Minimum 3–5 years of experience in the pharmaceutical industry
• Strong knowledge of ICH Stability Guidelines (Q1A, Q5C) and cGMP requirements
• Experience with stability studies, quality systems, and regulatory documentation
• Familiarity with statistical software such as JMP or SlimSTAT is an advantage
• Experience with LIMS and Quality Management Systems (e.g., TrackWise or Veeva)
• Strong analytical, organizational, and problem-solving skills
• Ability to work independently in a matrix organization
• Excellent communication skills in French and English