
QC Documentation Specialist
- Monza
- Tempo indeterminato
- Full time
- Collaborate with the team to review, draft, and issue the necessary specifications to ensure production quality.
- Manage internal change control processes to ensure seamless operations.
- Prioritize and complete assigned training to maintain the highest level of expertise and adherence to current procedures.
- Produce relevant documentation based on team needs and assigned priorities.
- Strictly adhere to data integrity rules and ensure all activities and data are in compliance.
- Bachelor's degree in scientific fields (CTF, Biology, Biotechnology, etc.).
- Minimum of 5 years of experience in pharmaceutical or biotech industries with a focus on documentation and good knowledge of GMP.
- Proficiency in Microsoft Office, PC usage, and document management systems.
- Good command of the English language.
- Ability to outline processes and documents.
- Knowledge of TrackWise and Documentum systems is preferred.
- Strong analytical skills
- Outstanding attention to detail
- Ability to work collaboratively in a team-oriented environment