via Indeed · 18. September 2026 ·vor 1 Tag

Technicien laboratoire contrôle qualité GMP (H/F/X)

Ekkiden
Lengnau BE Vollzeit
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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
What we are looking for:
  • 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

What we offer:

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.

You can also find all our job openings on our website

https://jobs.ekkiden.com/

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24 offene Stellen · Basel, Bern, Genève, Köln, Lengnau BE +5

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