Technicien laboratoire contrôle qualité GMP; H/F/X
Listed on 2026-09-21
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Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
International consulting group founded in 2019, Ekkiden brings together an ecosystem of passionate and committed consultants who lead organizational, operational, and technological transformation projects in IT/Digital, Industry/R&D, and sustainability, for large corporations and SMEs, in France, Switzerland, Spain, and Germany.
The role:As part of the strengthening of quality control activities within a pharmaceutical company, you will work as a QC laboratory technician in an environment subject to GMP requirements. You will carry out the analyses required to control raw materials, intermediate products and/or finished products, while ensuring compliance with procedures and regulatory requirements.
Responsibilities:- Perform quality control analyses in compliance with GMP and internal procedures
- Carry out physicochemical analyses on pharmaceutical samples
- Perform or participate in microbiological analyses according to laboratory needs
- Prepare samples, solutions, reagents and media required for analyses
- Use and maintain laboratory equipment
- Participate in investigations in case of atypical or out of specification results (OOS / OOT)
- Document analysis results in quality systems and files
- Ensure traceability and data integrity in accordance with GMP / data integrity requirements
- Participate in qualification, calibration and maintenance activities of laboratory equipment
- Draft and/or update laboratory documents and procedures
- Collaborate with QC, QA, production and engineering teams
- Degree such as CFC laborantin(e), bachelor's/master's in chemistry, biology, microbiology, pharmacy or equivalent qualification
- Minimum 5 to 10 years of experience in a pharmaceutical QC laboratory
- Significant experience in a GMP environment
- Good command of good laboratory practices (GLP)
- Knowledge of data integrity requirements
- Experience in managing OOS/OOT results
- German at operational/intermediate level (french is a plus)
- Rigorous, autonomous and quality oriented profile
- Ability to work in a regulated and documented environment
- Good team spirit and good communication skills
- Join us at the right time to make your mark within a rapidly growing organization
- Varied assignments in a challenging environment that will let you have a real impact on the company
- The opportunity to work autonomously and take initiative to grow together
- A career path tailored to your personality, both in terms of role and location
- Demanding, ongoing training to unlock your full potential
- A performance-driven culture with great results-based bonuses
- Comprehensive health insurance (GEREP) and meal vouchers (Swile card)
What does the recruitment process look like at Ekkiden?
At Ekkiden, we are committed to providing a positive experience for every candidate.
First contact:
Our recruitment team will reach out to discuss your motivations and expectations.
Interviews:
You will have one or two interviews with our business managers, depending on the position you're applying for.
Meeting the client:
Finally, you'll have the opportunity to meet the client.
While this is our standard process, we may adapt it depending on specific circumstances.
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