Scientist Jobs in Bern
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Scientist • bern
Senior Scientist QA Operations
LHHBern area, Switzerland, Bern area, Switzerland, SwitzerlandFull-Stack Developer With Leadership Skills
SWISSTRAFFIC AGIttigen, CHIT System Administrator / IT System Engineer 80-100%
nanoTRONIC AGLyss, Canton of Bern, SwitzerlandSpécialiste I + D et Data Scientist
Services du parlement SPBern, CHFlow Cytometry Specialist
Kanton BernBernScientist Stability Program QC
Bavarian Nordic Berna GmbHThörishaus, CHDevOps Engineer Entry Control
Die Schweizerische PostBern or Lausanne and home office (Berne), CHData Scientist
Alliance SwissPassBern, CH- Gesponsert
Data Scientist
WhatJobsBern, SchweizScientific Expert QC Excellence LIMS
Real StaffingBern, SwitzerlandData Scientist
Alliance SwissPassBern, CH- Gesponsert
Data Scientist
WhatJobsBern, Schweiz(Junior) Scientist - Pharma - Bioassays
EurofinsBern, BE, CHData Scientist
Universität BernBern, CHOperational Support Scientist
CSLEMEA, CH, Kanton Bern, Bern, CSL BehringData Scientist
Universität BernBern, CHData Scientist Energiesysteme
BKW Energie AGOstermundigen, CHDevOps Engineer Entry Control
Post CH AGBern oder Lausanne und Homeoffice, Region Bern, SwitzerlandÄhnliche Suchanfragen
Senior Scientist QA Operations
LHHBern area, Switzerland, Bern area, Switzerland, SwitzerlandNow Hiring : Senior Scientist QA Operations – Biologics Manufacturing
Are you ready to take your quality assurance expertise to the next level in a cutting-edge pharmaceutical environment? We’re looking for experienced QA professionals to join a high-impact team at a world-class biologics manufacturing site in Bern area, Switzerland.
The Opportunity
We currently have three open contractor positions for Senior Scientist QA Operations roles. The initial contract duration is six months, with a strong possibility of internalization for top performers. This is your chance to contribute to the production of life-changing therapies — and potentially secure a long-term future with a leading organization.
Key Responsibilities
- Ensure compliance with cGMP and pharmaceutical regulations across manufacturing activities
- Perform batch record reviews, deviation assessments, and change control evaluations
- Support technical batch release and provide on-the-floor QA oversight
- Review and approve key documentation such as SOPs, working instructions, and impact assessments
- Drive continuous improvement initiatives and support APQR execution
- Promote and uphold data integrity principles (ALCOA+)
Qualifications
Why Apply?
This is more than just a contract — it’s an opportunity to be part of a purpose-driven team helping to deliver high-quality medicines to patients worldwide. Contribute your expertise and grow your career in an innovative and collaborative environment.
Apply now and take the next step toward meaningful, mission-driven work.
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