GMP Manufacturing Process Improvement Professional

Vor 4 Tagen


Visp, Schweiz Capgemini Engineering Vollzeit

Capgemini Engineering is seeking a GMP Manufacturing Process Improvement Professional to join our team. As a key member of our pharmaceutical manufacturing operations, you will be responsible for identifying areas for process improvement and implementing changes to ensure efficient production and compliance with Good Manufacturing Practices (GMP) guidelines.

About the Job

The successful candidate will have extensive experience in bioprocesses, including monitoring, troubleshooting, and improving process efficiency. A strong background in biotechnology or a related field, as well as excellent problem-solving and analytical skills, is required. If you are passionate about process improvement and GMP, we encourage you to apply.

  • Main Responsibilities:
  • Identify areas for process improvement and implement changes to ensure efficient production and compliance with GMP guidelines.
  • Monitor and troubleshoot bioprocesses to identify areas for improvement.
  • Collaborate with cross-functional teams to develop and implement best practices.

Required Skills and Qualifications:

  • Bachelor's or Master's degree in Biotechnology, Bioprocess Engineering, Biochemistry, or a related field.
  • Extensive experience in bioprocesses, including monitoring, troubleshooting, and improving process efficiency.
  • Excellent problem-solving and analytical skills.

Why Join Us?

  • A permanent contract with a leading engineering consulting firm.
  • A multi-stage model with career opportunities through specialization prospects with over 250,000 consultants worldwide.


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