For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Laboratory Specialist - QC Microbiology.
General Information:
- Start Date: 01.04.2026
- Latest Possible Start Date: 01.06.2026
- Planned Employment Duration: 12 months contract with the possibility of extension
- Workplace: Kaiseraugst
- Workload: 100%
- Home Office: not possible, on site presence required
- Team: 20 People
- Department: MMQIAB8H QC mEMT Kaiseraugst
- Working Hours: Standard
About the job:
As a Laboratory Technician Specialist QC Microbiology within the "QC mEMT Kaiseraugst" group of pharmaceutical quality control, you will ensure reliable and efficient microbiological environmental monitoring for our manufacturing customers at the Kaiseraugst site, guaranteeing product safety and, consequently, patient well-being.
The ideal candidate:
Holds a degree in life sciences (e.g., biotechnology, microbiology, or bioengineering) and possesses at least two years of experience in the pharmaceutical industry within a GMP-regulated environment. They have in-depth knowledge of pharmaceutical quality systems, consistently act with a focus on quality and compliance, and demonstrate strategic thinking, the ability to take responsibility, and the capacity to reliably achieve results. Through their structured, team-oriented approach and fluency in German and English, they build trusting relationships and actively contribute to continuous process improvement.
Tasks & Responsibilities:
- Professional execution of special orders as well as general laboratory and service work according to the instructions of the Planning and Coordination Leader (PCL) or Unit Leads and their documentation in accordance with current Good Manufacturing Practice (cGMP) guidelines
- Ensuring competent, efficient, and GMP-compliant analytics by adhering to all relevant guidelines, SOPs, and regulatory and registration requirements
- Planning and controlling workflows for laboratory activities
- Creation and updating of test procedures, SOPs, and other GMP-relevant documents
- Handling of discrepancies (UPE)
- Support in the development and implementation of group strategies and objectives
- Taking on corresponding special tasks
Must Haves:
- Completed degree in the field of life sciences, e.g., biotechnology; microbiology; Bioengineer or comparable degree (Bachelor's or Master's)
- Preferably 2 years of experience in the pharmaceutical industry and in a GMP-regulated environment or comparable (e.g., as a microbiologist; QA Assistant)
- Expertise in pharmaceutical quality systems and standards
- Fluent German and English skills
- Taking responsibility, determination, and achieving expected results
- Building trusting and successful relationships
- Excellent organizational skills, strategic thinking, and the ability to translate strategies into actionable plans
- Team-oriented mindset with a focus on continuous process improvement and the ability to deliver consistent performance.
Nice to haves:
- Training/experience in microbiology and/or sterility assurance
- Strong understanding of quality and compliance and corresponding action.
Sounds interesting? Apply now – we’re looking forward to receiving your applications!
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