Question
FULL_TIME
5-10

Senior Scientist microbiological Quality Control

4/19/2026

The Senior Scientist will coordinate the transfer, development, and validation of analytical methods while ensuring full GMP compliance within the microbiological quality control laboratory. They will also manage projects, oversee laboratory troubleshooting, and provide SME review for protocols and reports.

Working Hours

40 hours/week

Company Size

10,001+ employees

Language

English

Visa Sponsorship

No

About The Company
About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com.
About the Role

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Location/Division Specific Information:

This position is part of the Microbiological Quality Control (MBQC) team from Thermo Fisher Scientific in Lengnau (CH), supporting GMP-regulated manufacturing operations. The role operates within a laboratory environment focused on ensuring microbiological quality and compliance of pharmaceutical products and processes.

Education & Experience:

  • Degree (Master or higher) in the Microbiology or Life Science Area

  • At least 5 years experience in microbiological laboratories including experience in a regulated GMP environment.

A Day in the Life:

  • Coordinate and work on the transfer, development and validation of analytical methods including qualification of equipment needed for analysis.

  • Actively contribute to the GMP Inspection Readiness of QC to ensure the fully compliance of relevant Quality System and Procedural documents.

  • Actively contribute to the QC operational readiness managing projects (external and internal) and the assigned to ressources (including coordination of people daily tasks). Participates in the transfer, development and validation of analytical methods including qualification of equipment needed for analysis.

  • Responsible for development, transfer and validation of analytical procedures professionally and according to timelines.

  • Ensure ready to state activities in the MBQC lab.

  • Collaboration in the solution of MBQC problematic and / or questions (quality problems, government inquiries, etc.).

  • Supporting of laboratory employee during troubleshooting activities.

  • Efficient communication: Informing the MBQC head in a timely manner regarding ongoing business activities, deviations, and problems within the team.

  • Responsible for writing and revision of standard operating procedures (SOPs) and instructions (Wis) professionally and according to timelines.

  • Responsible for SME review and approval of methods, plans, protocols and reports, gap assessments

Knowledge, Abilities:

  • Extensive knowledge of microbiological testing techniques (bioburden, endotoxin, qPCR) and laboratory best practices

  • Strong knowledge of cGMP requirements, method validation/verification, and documentation standards (SOPs, WIs)

  • Ability to troubleshoot microbiological issues, support investigations, and collab orate in cross-functional teams

  • Fluent English (written and spoken), German is a plus

What We Offer:

  • Compensation

  • Competitive Pay

  • Performance Related Bonus where eligible

  • Annual merit performance-based increase

Key Skills
MicrobiologyGMPAnalytical method validationBioburden testingEndotoxin testingqPCRLaboratory troubleshootingSOP writingQuality controlEquipment qualificationRegulatory complianceProject managementDocumentation standardsData analysisCross-functional collaboration
Categories
Science & ResearchManufacturingHealthcare
Benefits
Competitive payPerformance related bonusAnnual merit performance-based increase
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