Analytical Development & Gmp Documentation
Thermo Fisher Scientific · Monza, Provincia di Monza e Brianza
Job Description
About the Role
Thermo Fisher Scientific is seeking an Analytical Development & GMP Documentation Specialist to join our team in Monza, Italy. This is an onsite position where you will contribute to challenging work within a team that values performance, quality, and innovation. As part of a growing global organization, you will be encouraged to perform at your best and have the resources to make significant contributions.
Key Responsibilities
- Develop and optimize analytical methods.
- Prepare and review GMP (Good Manufacturing Practice) documentation.
- Ensure compliance with relevant regulations, including controlled drug regulations in Europe.
- Support Research and Development (R&D) activities through analytical expertise.
Requirements
- Experience in Analytical Development.
- Proficiency in GMP documentation and compliance.
- Strong understanding of R&D processes.
- Knowledge of controlled drug regulations in Europe is a plus.
About Thermo Fisher Scientific
Thermo Fisher Scientific is a world leader in serving science, with revenues of more than $40 billion. We enable our customers to make the world healthier, cleaner, and safer. We have the largest investment in R&D in the industry, providing our people with the resources and opportunities to make significant contributions.
✨ This description was enhanced by AI based on the original listing.