GMP QA Specialist – On-Site Production & Compliance

Haybury; Bern; On-site; CHF 75,000 - 105,000; Full time

Job summary

Haybury is supporting a leading biopharmaceutical manufacturer in Bern, Switzerland, by recruiting Quality Assurance professionals for long-term assignments. These hands-on, operational QA roles will closely interact with manufacturing to uphold GMP standards and product quality on-site in Bern.

Responsibilities include floor QA oversight, reviewing batch documentation, supporting change controls, GMP documentation maintenance, monitoring aseptic activities, and GMP training.

Qualifications

• QA experience in GMP-regulated manufacturing.
• Willingness to work early 05:00 starts or late shifts after 22:00.
• On-site role based in Bern, commuting availability essential.
• German proficiency suitable for GMP documentation work.

Responsibilities

• Provide quality oversight on the manufacturing floor.
• Review production and batch documentation.
• Support change controls.
• Review and maintain GMP documentation.
• Monitor aseptic manufacturing activities.
• Support GMP training.
• Work with production teams to resolve quality issues.

Skills

Quality Assurance

Documentation

Attention to detail

German language

GMP awareness

Education

Scientific degree or equivalent

Tools

Excel

Word

Job description

Haybury is supporting a leading biopharmaceutical manufacturer in Bern, Switzerland, by recruiting Quality Assurance professionals for long-term assignments. These hands-on, operational QA roles will closely interact with manufacturing to uphold GMP standards and product quality on-site in Bern.

Responsibilities include floor QA oversight, reviewing batch documentation, supporting change controls, GMP documentation maintenance, monitoring aseptic activities, and GMP training.