Quality Control Analyst
Quality Control Analyst
Posted on :
13-08-2025
Employer Active
1 Vacancy
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Hourly Salary
CHF CHF 40 - 40
Vacancy
1 Vacancy
Posted on :
13-08-2025
Job Description
Quality Control Analyst 6-month Contract) Join a Leading Pharmaceutical Team in Switzerland
Location: Switzerland
Start Date: ASAP
Contract Duration: 6 months
Rate: 40 CHF/hour gross
Position: 1 vacancy
Are you a detail-oriented laboratory professional with hands-on expertise in biochemical methods? Do you thrive in fast-paced, high-quality environments where precision matters? If so, we want to hear from you!
About the Role
As a Quality Control Analyst, you will play a key role in ensuring the highest standards of product quality in a cGMP-regulated pharmaceutical environment. You will perform a variety of biochemical analyses including ELISA, enzyme activity tests, Western Blot, and HPLC while maintaining rigorous compliance with GMP, documentation standards, and safety rules.
Key Responsibilities:
Location: Switzerland
Start Date: ASAP
Contract Duration: 6 months
Rate: 40 CHF/hour gross
Position: 1 vacancy
Are you a detail-oriented laboratory professional with hands-on expertise in biochemical methods? Do you thrive in fast-paced, high-quality environments where precision matters? If so, we want to hear from you!
About the Role
As a Quality Control Analyst, you will play a key role in ensuring the highest standards of product quality in a cGMP-regulated pharmaceutical environment. You will perform a variety of biochemical analyses including ELISA, enzyme activity tests, Western Blot, and HPLC while maintaining rigorous compliance with GMP, documentation standards, and safety rules.
Key Responsibilities:
- Perform biochemical analyses and supervise activities in line with laboratory procedures & GMP/BPD standards.
- Complete documentation in compliance with Good Manufacturing & Documentation Practices (ALCOA .
- Immediately report and document non-compliant or invalid results.
- Conduct laboratory investigations and participate in troubleshooting.
- Qualify and validate reagents, consumables, methods, systems, and equipment.
- Maintain equipment calibration and Kanban real-time management.
- Support continuous improvement and maintain 5S workplace organization standards.
- CFC in laboratory/biology or relevant scientific field.
- Minimum 3 years QC laboratory experience in a cGMP environment.
- Proficiency in Electrophoresis, HPLC, ELISA, or enzymatic activity analysis.
- Strong organizational skills and quality-oriented mindset.
- Fluent in French & technical English.
- Swiss/EU nationality or valid Swiss work permit.
Employment Type
4
Company Industry
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