Associate Scientist (H/F) - CDI
MERCK SERONO SA Vacant since: 06.05.2026 Number of jobs: 1 1809 Fenil-sur-Corsier (VD) 100% Immediately Permanent Registration requirement
The Biotech Development Center (BDC) is our Company's flagship biotech investment in line with the ambition to stay the Vibrant Science and Technology Company. The BDC is integrating analytical technologies of the future with high‑tech automatized and digital laboratories, in a flexible, agile and highly collaborative environment.
Your role: Reporting to the “Analytical Operations & Quality Control Lab Manager” in the Global Analytical Development organization, this role represents an opportunity to significantly contribute to high‑tech GMP analytical laboratories in the BDC, by proactively designing/executing new workflows in a cross‑functional set up. You liaise with peer QA, QC and manufacturing colleagues and you allow smooth analyses execution as well as documentation management and troubleshooting eager to develop in a context of growth, simplification, and changes to ensure the delivery of our specialty innovator Biotech pipeline to patients.
Key Responsibilities
Conduct routine analytical testing and method qualification, including stability, independently in at least two areas: Liquid Chromatography, Capillary Electrophoresis, and MS‑based methods.
Deliver high‑quality data treatment/elaboration and analytical reports in a digitally agile manner.
Interact with customers as needed to discuss results or coordinate routine/validation activities.
Work autonomously on routine or non‑routine activities within established procedures, applying specialized technical knowledge (e.g., stability).
Demonstrate strong expertise in a GMP environment.
Validate GMP methods including analysis and documentation; method validation knowledge is mandatory.
Actively seek, share, and re‑apply knowledge within own field; lead analytical workflow improvement initiatives in a cross‑functional setting.
Present and defend topics during health authority inspections; write GMP documentation (URS, protocols, reports, SOPs, deviations, CAPA, CCP actions).
Who You Are
Degree: CFC or Master in Chemistry, Pharmacy, Biology, or Biotechnology; ≥5 years in a GMP analytical lab.
Proficient with (L)LIMS; Empower and/or Waters Connect a plus.
Comfortable writing GMP analytical protocols, reports, and SOPs.
Strong knowledge of Liquid Chromatography and/or Mass Spectrometry (routine testing, troubleshooting, cleaning).
Knowledge of CMC NBE/ADC development; ADC knowledge is a strong asset.
Familiar with GMP/Quality Systems and international guidelines (ICH, Pharmacopeias).
Capable of performing routine and non‑routine analyses; able to sort deviations, CAPA, and lead investigations for QC.
Team player with solid English; French a plus; curious about new tools/tech; proactive in proposing solutions and driving improvements; on‑call duties; 6S experience; strong planning.
Work Details
Work location 1809 Fenil-sur-Corsier (VD)
Workload 100%
Employment start Immediately
Employment duration Permanent
Qualification skilled
Work experience More than 3 years
Education Vocational education and training with the Swiss Federal VET Diploma or equivalent
English (orally) Very good knowledge
English (written) Very good knowledge
Application method Online form
To apply: https://careers.merckgroup.com/global/en/job/MQAMKDGLOBAL298824EXTERNALENGLOBAL/Associate-Scientist---All-Genders
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