Become Thermo Fisher Scientific Inc.'s Sr Administrative Services Coordinator in a dedicated team improving global health and safety.
Typical work hours for this role will be either 7:00am - 3:30pm or 8:00am - 4:30p. There will also be mandatory OT on Saturdays as needed by the business.
Job Responsibilities
Provide direct support to Production, ensuring strict adherence to Good Manufacturing Practice (GMP) standards.
Evaluate batch record documentation and collaborate with Production and Quality Assurance to resolve any discrepancies in compliance with current GMP (cGMP) requirements.
Assure regulatory compliance and process improvement by assessing production processes, operations, and materials.
Act as a GMP resource for internal collaborators, avoiding regulatory liabilities and preserving client happiness.
Conduct detailed analysis on batch record data, tracking errors and improving process flow for efficiency and accuracy.
Uphold a safe workplace, adhering strictly to all safety protocols and training requirements.
Requirements
High School diploma or equivalent minimally required.
Minimum experience required is 2 years of GMP pharmaceutical batch record processing; Four years of relevant experience is preferred
Knowledge, Skills, Abilities:
Outstanding attention to detail and organizational skills.
Self-sufficient, reliable, and skilled at managing multiple tasks in a fast-paced environment.
Strong verbal and written communication skills.
Collaborative great teammate capable of leading and contributing effectively.
Physical Requirements
Ability to perform ordinary ambulatory skills and physical coordination.
Capable of lifting, carrying, and moving weights of 10-35 pounds periodically.
Prolonged periods of standing, walking, stooping, kneeling, and crouching.
Proficient in keyboard and computer operations, with the ability to sit, reach, talk, and hear for extended durations.
Join us and make a difference with your outstanding skills and dedication!