Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

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.

Description

• Support the establishment and operational readiness of the Bio-/Chemical Quality Control (BCQC) unit at the Thermo Fisher Lengnau site in alignment with project timelines and GMP requirements.
• Contribute to the transfer, development, and validation of analytical methods, including qualification of analytical equipment.
• Actively ensure GMP inspection readiness by supporting compliance with applicable quality systems, procedures, and regulatory requirements.
• Participate in internal and external inspections (e.g., regulatory and customer audits), including preparation, support during inspections, and follow-up activities.
• Perform reviews of analytical data to ensure accuracy, completeness, and compliance with GMP and ALCOA+ principles.
• Participate in internal and external QC-related projects, coordinating resources and managing daily operational activities to support efficient laboratory execution.
• Offer opportunities for professional growth while working with skilled colleagues who share our commitment to excellence and innovation.

Requirements

• Preferred Bachelor's degree, no prior experience required. Experience in quality control laboratory environment, preferably in pharmaceutical/biotech industry preferred
• Preferred Fields of Study: Chemistry, Biochemistry, Biology, Molecular Biology or related scientific field
• Strong knowledge of cGMP, GLP, and quality management systems
• Proficiency in Biochemical and chemical analytical techniques such as HPLC, ELISA etc.
• Ability to follow and write SOPs and maintain detailed documentation per GDP requirements
• Strong computer skills including LIMS, Microsoft Office, and analytical software
• Excellent attention to detail and organizational skills
• Strong analytical and problem-solving capabilities
• Ability to work both independently and collaboratively in a team environment
• Clear written and verbal communication skills
• Experience with laboratory equipment maintenance and calibration
• Knowledge of relevant pharmacopeia standards and regulatory requirements
• Ability to manage multiple priorities effectively