• Prestigious pharmaceutical company
  • Temporary contract until the end of the year (Extension possible)

About Our Client

Our client, a leading global pharmaceutical/biotech company, is currently seeking a QA Specialist to support projects in the Solothurn area, with an initial contract until the end of 2026

Depending on the candidate's expertise and commitment, an extension of the assignment or further opportunities within the organization may be possible.

Job Description

• Responsible for the Quality Management Systems (QMS) across multiple sites.
• Manage and process deviations, CAPAs, and change records in compliance with GMP requirements.
• Act in a global function to support the continuous improvement and harmonization of QMS across different sites.
• Support inspection readiness activities and participate in internal audits.

The Successful Applicant

• 3-5 years of experience in a similar Quality Assurance or QMS-related role.
• Experience in a pharmaceutical or biotech environment with strong knowledge of GMP regulations.
• Hands-on experience in CAPA management, deviation handling, and change control.
• Fluent English; German is an advantage.
• Confident working with digital tools and reporting solutions, such as Power BI.

What's on Offer

Want to join a leading company in the Life Sciences, where you can use your QA Skills?
Looking forward to your application.

Quote job ref

JN-012026-6934787

Job Function

Healthcare & Life Sciences

Specialisation

Biotechnology

Industry

Healthcare / Pharmaceutical

Location

Solothurn

Contract Type

Interim

Job Reference

JN-012026-6934787

Job Nature

Home Office