Quality Specialist (m/f/d)

About the job

unisite ag is a service provider in the field of Employer Branding & Talent Management. We provide consulting services to clients in the chemistry, pharmaceutical, biotech, medical device, and life sciences industries.

Our client, Solvias AG, is a global cGMP Contract Research Organization (CRO) with a comprehensive portfolio of analytical services for the pharmaceutical, biotech and life sciences industry.

On behalf of our client, we are currently looking for a:

Quality Specialist (m/f/d) – 100% | 6-9 Months

Location: Kaiseraugst, AG

Duration: ca. 6-9 Monate

Tasks

Manage QC deviations, CAPAs and change controls

Conduct root cause investigations

Maintain and update controlled documents such as SOPs, test methods and forms

Support the implementation of CAPA actions

Ensure data integrity and proper documentation

Perform risk assessments related to QC processes

Monitor quality metrics and deviation trends

Collaborate closely with QC laboratories and QA teams

Qualification

Experience in pharmaceutical Quality Control or contract laboratory services

Strong knowledge of GMP regulations and data integrity principles

Experience conducting investigations and root cause analyses

Familiarity with analytical methods and QC workflows in regulated environments

Strong communication skills and ability to collaborate with QC and QA stakeholders

Structured, proactive and solution-oriented mindset

Excellent documentation and technical writing skills

Very good command of English is required, German or French is a plus

Take this opportunity to shape your future – we look forward to your application!