QC Specialist
Date de publication :
16 avril 2025Taux d'activité :
100%- Lieu de travail :Bulle
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Résumé de l'emploi
Rejoignez UCB à Bulle, Suisse, en tant que spécialiste QC. Une opportunité enrichissante vous attend dans un environnement dynamique.
Tâches
- Agir en tant qu'expert en méthodes analytiques et équipements de laboratoire.
- Soutenir les équipes QC dans les opérations et la résolution technique.
- Contribuer aux investigations, CAPA et révisions de qualité.
Compétences
- Diplôme en biologie, biochimie ou chimie et 5 ans d'expérience QC.
- Connaissance des normes GMP, GLP et pharmacopées.
- Capacité à travailler en équipe avec un style autonome.
Est-ce utile ?
Location: Bulle, Switzerland
Activity rate: 100%
Contract: temporary contract
Start date: 02.06.2025
Duration: 12 months
UCB, one of Switzerland's Best Employers, is an internationally active biopharmaceutical company specialising in the therapeutic areas of neurological disorders and immunology. The Bulle site is home to the company's Swiss sales subsidiary and primarily a biotechnological and chemical production platform for the manufacture and distribution of pharmaceutical specialities for the treatment of allergy, epilepsy and autoimmune diseases.
To support the QC team at UCB's Bulle site in Switzerland, we are looking for a 100% QC Specialist.
Your key responsibilities:
As a QC Biologics Specialist, you will be a key player in supporting laboratory activities, ensuring compliance, and driving continuous improvement across QC processes. Your main responsibilities will include:
- Act as SME for analytical methods and lab equipment
- Support QC teams in daily lab operations and technical troubleshooting
- Lead or contribute to deviations, CAPA, and investigations
- Draft and revise SOPs, reports, specifications, and quality documents
- Participate in the implementation and qualification of new methods/equipment
- Ensure compliance with GMP, GLP, and internal quality standards
- Prepare and support regulatory inspections and internal audits
- Contribute to Product Quality Reviews (PQR) and CPV activities
- Identify improvement opportunities and lead related initiatives
- Collaborate with cross-functional teams (QA, Manufacturing, Supply Chain, etc.)
- Provide input on equipment budgets and investment planning
- Ensure inspection readiness and maintain accurate documentation
- Act as back-up for other QC Specialists when needed
- Help define and implement QC strategies for analytical processes
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qualifications
What will make you successful:
- Bachelor's or Master's degree in Biology, Biochemistry, Chemistry, or related field
- Minimum 5 years' experience in QC within the pharma/biotech industry
- Solid knowledge of GMP, GLP, and major pharmacopoeias (EP, USP/NF, JP)
- Proficiency in analytical techniques: HPLC, UPLC, ELISA, bioassays, microbiology
- Good understanding of statistics, process capability, and problem-solving tools
- Experience with QA processes: deviations, CAPA, investigations
- Fluent in French and English (written and spoken)
- Strong organizational skills: able to plan, prioritize, and meet deadlines
- Team-oriented with a calm, structured, and autonomous working style
- Comfortable leading small projects and training peers when needed
UCB is committed to fostering a diverse, inclusive, and equitable workplace where everyone's talents and perspectives are valued and respected.
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Laetitia Stirer
- Randstad UCB Bulle
