QC Specialist - Randstad - HELP
Jobdescription
Location: Bulle,Switzerland
Activity rate:100%
Contract: temporarycontract
Start date:02.06.2025
Duration: 12 months
UCB, one of Switzerland's Best Employers, is aninternationally active biopharmaceutical company specialising inthe therapeutic areas of neurological disorders and immunology. TheBulle site is home to the company's Swiss sales subsidiary andprimarily a biotechnological and chemical production platform forthe manufacture and distribution of pharmaceutical specialities forthe treatment of allergy, epilepsy and autoimmunediseases.
To support the QCteam at UCB's Bulle site in Switzerland, we are looking for a 100%QC Specialist.
Your keyresponsibilities:
As a QC Biologics Specialist,you will be a key player in supporting laboratory activities,ensuring compliance, and driving continuous improvement across QCprocesses. Your main responsibilities willinclude:
- Act as SME for analyticalmethods and lab equipment
- Support QC teams indaily lab operations and technicaltroubleshooting
- Lead or contribute todeviations, CAPA, and investigations
- Draft andrevise SOPs, reports, specifications, and qualitydocuments
- Participate in the implementation andqualification of new methods/equipment
- Ensurecompliance with GMP, GLP, and internal qualitystandards
- Prepare and support regulatoryinspections and internal audits
- Contribute toProduct Quality Reviews (PQR) and CPVactivities
- Identify improvement opportunitiesand lead related initiatives
- Collaborate withcross-functional teams (QA, Manufacturing, Supply Chain,etc.)
- Provide input on equipment budgets andinvestment planning
- Ensure inspection readinessand maintain accurate documentation
- Act asback-up for other QC Specialists whenneeded
- Help define and implement QC strategiesfor analytical processes
Qualifikationen
What will make yousuccessful:
- Bachelor's or Master'sdegree in Biology, Biochemistry, Chemistry, or relatedfield
- Minimum 5 years' experience in QC withinthe pharma/biotech industry
- Solid knowledge ofGMP, GLP, and major pharmacopoeias (EP, USP/NF,JP)
- Proficiency in analytical techniques: HPLC,UPLC, ELISA, bioassays, microbiology
- Goodunderstanding of statistics, process capability, andproblem-solving tools
- Experience with QAprocesses: deviations, CAPA,investigations
- Fluent in French and English(written and spoken)
- Strong organizationalskills: able to plan, prioritize, and meetdeadlines
- Team-oriented with a calm,structured, and autonomous workingstyle
- Comfortable leading small projects andtraining peers when needed
UCB is committed to fostering a diverse,inclusive, and equitable workplace where everyone's talents andperspectives are valued and respected.