Quality Associates - GMP ( x1Jr. / x1 with 3 years Exp.)

Project overview

Are you a German-speaking GMP professional with a passion for quality and compliance in pharmaceutical manufacturing?

Proclinical is seeking Quality Associates to support quality assurance activities within the pharmaceutical industry. This role focuses on ensuring compliance with GMP standards and maintaining high-quality processes in a cardiovascular therapy area. We are hiring for two positions: one junior-level role and one experienced role. Both positions require a proactive approach, attention to detail, and strong collaboration with production teams.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities

• Manage deviations and implement change management processes.
• Conduct quality assurance activities on the production floor.
• Provide training and administrative support to the team.
• Review PRO-QA documentation and batch records.
• Monitor aseptic processes and ensure compliance with GMP standards.
• Utilize IT systems such as Excel, Word, OneNote, and AI tools effectively.

Requirements

For the Experienced Quality Associate:

For the Junior Quality Associate:

If you are having difficulty in applying or if you have any questions, please contact Olivier Worch at [contact removed].

Apply Now:

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• Native German speaker.
• Proven GMP experience in Quality Assurance.
• University degree in Science (Bachelor's, Master's, or PhD).
• Ability to travel to Bern within one hour.
• GMP experience, preferably in Quality Assurance.
• If no scientific degree, at least 5 years of GMP experience required.
• Availability for early morning shifts (starting at 05:00) and/or late evening shifts (after 22:00).
• Strong proficiency in Excel, Word, OneNote, and other IT systems.

Project details

• Start: flexible
• Location: Berne, Switzerland, CH