Quality Assurance Specialist - Pharma

☞ Consultys CH

View: 179

Update day: 14-04-2024

Location: Bern Bern BE

Category: Quality Assurance / Quality Control Production / Operation Consulting / Customer Service

Industry: Business Consulting Services Biotechnology Research Pharmaceutical Manufacturing

Position: Associate

Job type: Full-time

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Job content

Consultys is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry.

Since 2005, Consultys has been working on technical projects with some of the most sophisticated, innovative, and successful Life Sciences companies.

Our 650 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, France and Canada.

Thanks to our excellent team, we support manufacturers in all stages of drug development.

Respect, transparency, and gratitude.

These are the values that made Consultys one of the most high-performing Life Sciences consulting companies.

Do you want to be part of a human-sized company that values every individual?

Do you want to work on long-term innovative projects, working closely with global Life Sciences product companies in the world?

Join us!

We offer an attractive salary and benefits. You will work in a stimulating environment, with a lot of opportunities for your professional and personal development.

Your tasks:

  • Within the quality operations department, the Quality Assurance Expert assures that all operations meet or exceed cGMP regulations ensuring the quality of Drug Substance
  • Responsible for root cause analysis and corrective action for product and process-related deviation / non-conformances related to the biotech production
  • Responsible for quality operations including Change Control review, Batch records review, review/audit of data and reports as specified by Standard Operating Procedures

Your profile:

  • Bachelor’s degree or Master’s degree is needed, preferably in a scientific topic (Pharmacy, Chemistry, Biology, Biotechnology, etc.)
  • At least 1 year of experience in Quality Assurance/Quality Operations in the pharmaceutical or biotech industry
  • Excellent knowledge of regulatory requirements, including GMP guidelines
  • Previous experience with systems like Trackwise, MES
  • Excellent knowledge of English
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Deadline: 29-05-2024

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