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

Quality Assurance Opportunity in Pharmaceutical Manufacturing

Proclinical is seeking dedicated 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 the 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. 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.

Key Skills and Requirements

For the Experienced Quality Associate

• 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.

For the Junior Quality Associate

• Native German speaker.
• 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.