QC Software Specialist

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, No eye contacts allowed; prescriptive glasses will be provided, Office

Job Description

Are you ready to make an exceptional impact in the world of science? Join Thermo Fisher Scientific as a QC Software Specialist in our world-class Quality Control team based at our PSG Large Molecule site in Lengnau. Be a part of our ambitious mission to enable our customers to make the world healthier, cleaner, and safer through flawless execution and innovative solutions.

What will you do?

Discover Impactful Work:

The QC Software Specialist ensures that processes, analytical equipment, and related applications align with health authority requirements. Key responsibilities include:

Want more jobs like this?

Get jobs in Grenchen, Switzerland delivered to your inbox every week.

Get Jobs

Send me The Muse newsletters for the best in career advice and job search tips.

By signing up, you agree to our Terms of Service & Privacy Policy.

• Managing the lifecycle of QC systems, providing first & second-level support to meet customer and health authority expectations.
• Participating in the qualification of analytical equipment, including Computer System Validation (CSV).
• Delivering timely support to QC lab units for the investigation and resolution of OOX, change controls, and deviations.
• Engaging in gap assessments and actions related to inspection/audit readiness for health authorities and customer audits, including active participation during such inspections.

• A Bachelor's or Master's degree in Molecular Biology, Chemistry, Biochemistry, Chemical Engineering, or a related field is required. Equivalent experience in these fields will also be considered.
• Alternatively, an IT/Automation background with proven experience in the pharma industry.

• Proficiency with applications of analytical equipment, including Computer System Validation (CSV)
• Familiarity with Lab Execution Systems such as SM LIMS, Chromeleon, Lab X, Empower, etc. is a plus
• Experience in a GMP laboratory environment including Computer System Validation (CSV) is a plus
• Technical English required, German is a plus.

• Passionate about the digitalization of systems.
• Proficient in working effectively across different functions.
• High attention to detail.
• Ability to work independently with excellent communication and prioritization skills.
• Strong desire to learn new skills and successfully implement them.