QA Specialist - Deviations, Change Control & Quality Systems

About the role

Swisslinx AG is recruiting two GMP Compliance Specialists on behalf of its client, an international pharmaceutical company, based in Bern. The role supports deviation management, change control, documentation and risk assessments in a GMP-regulated environment. It is a temporary, part-time position starting on 1 December 2026, lasting about 7 months, with a workload of 41 hours per week; remote work is possible.

Key responsibilities

• Investigate deviations and prepare deviation reports
• Create and coordinate change requests, ensuring timely follow-up of required actions
• Create and update SOPs, procedures and work instructions
• Conduct risk assessments, including FMEA

Required profile

• Degree in Life Sciences (e.g. Pharmacy, Chemistry, Biology) or several years of relevant professional experience
• Initial experience in the pharmaceutical, chemical or food industry within a GMP environment
• Experience in at least one of: deviation management, change control, SOP documentation or risk assessments
• Independent working style, quick learner and ability to adapt to new topics
• Strong communication and teamwork skills, able to engage stakeholders
• German at C2 level or equivalent (mandatory) and good written and spoken English