Quality Assurance Associate

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

We're supporting a leading biopharmaceutical manufacturing organisation in Bern with the appointment of Quality Assurance professionals for a long-term assignment.

These are hands-on, operational QA positions, working closely with manufacturing colleagues to maintain GMP standards and product quality.

The work may include

• Providing Quality oversight on the manufacturing floor
• Reviewing production and batch documentation
• Supporting change controls
• Reviewing and maintaining GMP documentation
• Monitoring aseptic manufacturing activities
• Supporting GMP training
• Working closely with production teams to resolve quality issues
• Experience working within a GMP-regulated environment
• QA experience for the experienced position
• Scientific degree or equivalent relevant experience depending on profile
• Strong documentation and attention to detail
• German proficiency appropriate to working with production teams and GMP documentation
• Confidence using common business IT systems including Excel and Word

For our more operational profile, candidates must also be comfortable spending considerable time within manufacturing areas and be able to accommodate early starts from 05:00 and/or late shifts after 22:00.

The position is based on site in Bern, Switzerland, so practical commuting availability is important.

If your background is in pharmaceutical QA, quality operations or GMP manufacturing and you're interested in a production-facing Quality role, we'd be pleased to hear from you.