For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Laboratory Specialist in QC Microbiology.
General Information:
- Start Date: 01.01.2027
- Latest possible start date: 01.02.2027
- Planned Employment Duration: 6 months with the possibility of extension
- Workplace: Kaiseraugst
- Workload: 65%
- Home Office: Not possible
- Department: MMQIAB8H QC mEMT
- Working Hours: Standard, occasional weekend/holiday shifts
About the job:
As a Laboratory Specialist QC Microbiology in the "QC mEMT Kaiseraugst" group within Pharmaceutical Quality Control, you will ensure reliable and efficient microbiological environmental monitoring for our manufacturing clients at the Kaiseraugst site, safeguarding the quality of our products and ultimately the well-being of patients.
The Ideal Candidate:
The ideal candidate holds a completed degree in life sciences (e.g., biotechnology, microbiology, or bioengineering) and has at least two years of experience in the pharmaceutical industry within a GMP-regulated environment. They bring in-depth knowledge of pharmaceutical quality systems, consistently act with a quality- and compliance-oriented mindset, and demonstrate strategic thinking along with the ability to take ownership and reliably deliver results. Through a structured, team-oriented approach to work and fluent German and English skills, they build trusted relationships and actively contribute to continuous process improvement.
Tasks & responsibilities:
- Initiate and process Deviation Reports (DRs) and assessments, including alignment with relevant cross-functional interfaces and QA.
- Oversee the end-to-end deviation process from initiation upon detection, through Root Cause Analysis (RCA) and 5-Why analysis, to recurrence prevention via implementation of required Corrective and Preventive Actions (CAPA).
- Plan, coordinate, and document Change Requests for processes and methods within the unit.
- Author and update test procedures, SOPs, and other GMP documentation.
- Professionally execute specialized assignments as well as routine laboratory and service tasks according to instructions from the Planning and Coordination Leader (PCL) or Unit Lead, documenting them in accordance with current Good Manufacturing Practice (cGMP) guidelines.
- Ensure competent, high-performing, and GMP-compliant analytics by adhering to all relevant guidelines, SOPs, as well as regulatory and registration requirements.
- Plan, coordinate, and participate in cross-functional projects within QC and in collaboration with manufacturing clients.
- Willingness to work occasionally on public holidays.
Must Haves:
- Completed degree in the life sciences (e.g., Biotechnology, Microbiology, Bioengineering, or equivalent degree; Bachelor’s or Master’s)
- Preferably 2 years of experience in the pharmaceutical industry within a GMP-regulated environment or equivalent (e.g., as a Microbiologist, QA Assistant)
- In-depth knowledge of pharmaceutical quality systems and standards
- Fluent in German and English
- Accountability, decisiveness, and track record of delivering expected results
- Ability to build trusting and successful relationships
- Strong organizational skills, strategic thinking, and ability to translate strategies into actionable plans
- Team-oriented mindset focused on continuous process improvement and consistent performance
Nice-to-Haves:
- Education/experience in microbiology and/or sterility assurance
- Strong understanding of quality and compliance, acting accordingly
Sounds interesting? Apply now – we’re looking forward to receiving your applications!
Application Submission Deadline: 02.11.2026
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