Sr Administrative Service Coordinator

Thermo Fisher Scientific•Greenville, NC
•Onsite

About The Position

As part of Thermo Fisher Scientific, the Sr Administrative Service Coordinator provides administrative and operational support across document control, compliance management, and inventory coordination. The role works in a GMP environment, evaluating batch records, ensuring regulatory compliance, and serving as a liaison among Production, Quality Assurance, and other departments. Responsibilities include document management and review processes and maintaining detailed tracking systems while upholding accuracy and quality standards. The position supports pharmaceutical manufacturing operations and offers the opportunity to develop expertise in a highly regulated industry.

Requirements

  • At least 2 years of experience in pharmaceutical manufacturing, compliance, document control, or a related field.
  • Demonstrated expertise in GMP documentation review and compliance procedures.
  • Strong attention to detail and organizational skills.
  • Proficiency with enterprise software systems, including SAP, One Maximo, and document management systems.
  • Strong computer skills, including Microsoft Office Suite (Word, Excel, Outlook).
  • Effective written and verbal communication abilities.
  • Ability to work independently and as part of a team.
  • Ability to manage multiple priorities in a deadline-driven environment.
  • Experience with record review and documentation processes.
  • Ability to stand, walk, and stoop periodically; lift or carry 10–35 pounds occasionally; use a computer workstation for extended periods; and maintain visual focus on detailed documentation.

Nice To Haves

  • Preferred fields of study: Business, Science, or a Technical Field.
  • Knowledge of FDA regulations and cGMP requirements.

Responsibilities

  • Provide administrative and operational support across document control, compliance management, and inventory coordination.
  • Evaluate batch records and ensure regulatory compliance in a GMP environment.
  • Serve as a liaison between Production, Quality Assurance, and other departments.
  • Manage documents and review processes.
  • Maintain detailed tracking systems while upholding standards of accuracy and quality.
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