Qc Documentation Specialist

: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.Requirements: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.Thermo Fisher Scientific is an Equal Opportunity Employer.
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