Laboratory Employee Quality Control (m/w/d)

Sei unter den ersten Bewerbenden.
TN Germany
Penzberg
EUR 40.000 - 65.000
Sei unter den ersten Bewerbenden.
Gestern
Jobbeschreibung

Penzberg, Germany

At Roche, we embrace individuality and foster a culture of open dialogue, where everyone is valued and respected. Our mission is to prevent, stop, and cure diseases, ensuring access to healthcare for all, now and in the future. Join Roche, where your voice matters.

About Roche in 50 Words

Our goal is a healthier future through innovation. We advance science to provide essential healthcare, creating a world where we spend more time with loved ones. That is what makes us Roche.

What You Can Expect

In Pharma Biotech Penzberg, the Quality Control Virus & PCR department is responsible for in-process control and release of biotechnological active substances. As a Laboratory Technician (m/w/d) in Quality Control, your tasks typically include:

  1. Performing and documenting GMP-compliant molecular biological PCR analyses and cell-based virus detection methods for QC release of biotechnological products from European and Asian production sites.
  2. Developing, GMP-optimizing, and validating PCR/NAT and virus detection methods, including documentation, possibly in collaboration with other units.
  3. Participating in process transfers, process validations, method transfers, reagent qualification, troubleshooting, and regulatory submissions.
  4. Providing timely and accurate support for discrepancies, planned changes, and improvement measures.
  5. Implementing quality assurance measures and supporting laboratory organization, including reagent qualification, system maintenance, training, calibration, and equipment cleaning.

Who You Are

For this position, you should have:

  • A completed scientific education, preferably as a biology or chemistry laboratory technician (m/w/d), CTA (m/w/d), BTA (m/w/d), or comparable qualification.
  • Ideally, experience in pharmaceutical quality control.
  • Practical experience in cell culture, molecular biology, microbiology, and hygiene is advantageous.
  • Familiarity with GMP environments and a positive attitude towards working in such settings.
  • Proficiency with standard IT systems and good English skills.
  • Enjoyment of teamwork, motivation, and the ability to work independently, responsibly, and conscientiously.

This position is fixed-term for two years. Please upload only your CV online; no cover letter or certificates are needed at this stage. We look forward to your application!

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