Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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:
Be part of our Quality Control team at Thermo Fisher Scientific, where you'll contribute by ensuring the quality and reliability of products that help make the world healthier, cleaner and safer. You'll perform the set-up of stability study's, and report the results to support the development of innovative therapeutic products. You'll conduct the outsourced quality control testing of in-process samples, finished products and stability samples by managing the shipments to the external party. You'll document and analyse outsourced test results, participate in investigations, and contribute to continuous improvement initiatives. This role offers opportunities for professional growth while working with skilled colleagues who share our commitment to excellence and innovation.
REQUIREMENTS:
• Bachelor's degree. 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
• Experience with microbiological testing methods and aseptic techniques
• Ability to follow 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
• Knowledge of relevant pharmacopeia standards and regulatory requirements
• Ability to manage multiple priorities effectively
• Flexible scheduling may be required