QC Analyst
QC Analyst
- Art der Anstellung: Vollzeit
- 73.000 CHF – 100.500 CHF (von XING geschätzt)
- Hybrid
- Zu den Ersten gehören
QC Analyst
Über diesen Job
- Job type: Contract
- Discipline: Good Manufacturing Practice (GMP)
- Location: Switzerland
Proclinical is seeking a QC Analyst to support quality control activities in a pharmaceutical laboratory setting. This role involves performing analyses and sampling within a GMP-compliant environment, contributing to the establishment of a new production facility. You will play a key role in ensuring compliance with procedures, safety guidelines, and quality standards while supporting continuous improvement initiatives.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Conduct laboratory analyses and approvals following applicable procedures, cGMPs, and pharmacopoeias.
- Adhere to SOPs and maintain accurate documentation in line with Good Manufacturing Practices (GMP).
- Report non-conformities or invalid results promptly and initiate quality events as required.
- Ensure compliance with EHS (Environmental, Health, and Safety) regulations and actively promote adherence among colleagues.
- Execute qualification protocols for reagents, consumables, methods, systems, and equipment.
- Perform data entry, result supervision, and reconciliation of controlled documents.
- Support equipment maintenance, calibration, and troubleshooting activities.
- Participate in continuous improvement initiatives, risk analyses, and periodic system reviews.
- Train team members on equipment and GMP practices, acting as a backup trainer when needed.
- Collaborate with external partners, suppliers, and internal departments to ensure quality standards are met.
- Present expertise during inspections or audits and contribute to regulatory submissions.
Key Skills and Requirements:
- Background in microbiology or equivalent experience in the pharmaceutical or biotechnology industry.
- Familiarity with laboratory methods, cGMP standards, and data integrity principles.
- Proficiency in standard office software (e.g., Microsoft Office) and technical English (B2 level minimum).
- Strong organizational skills, teamwork orientation, and effective communication abilities.
- Commitment to upholding company values such as honesty, integrity, fairness, and perseverance.
- Fluency in French and technical English is essential.
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.
Apply Now:
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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