Sr Administrative Coordinator

Thermo Fisher ScientificGreenville, NC
Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges. In this role, you will provide administrative and operational support across document control, compliance management, and inventory coordination within a GMP environment. You will evaluate batch records, ensure regulatory compliance, and serve as a liaison between Production, Quality Assurance, and other departments while maintaining high standards of accuracy and quality.

Requirements

  • High school diploma or equivalent required.
  • 2+ years experience in pharmaceutical manufacturing, compliance, document control, or related field
  • Strong attention to detail and organizational skills
  • Strong Microsoft Office skills (Word, Excel, Outlook)
  • Effective written and verbal communication skills
  • Ability to work independently and within a team
  • Ability to manage multiple priorities in a deadline-driven environment
  • Ability to stand, walk, and stoop periodically
  • Lift/carry 10–35 pounds occasionally
  • Use computer workstation for extended periods
  • Maintain visual focus on detailed documentation
  • Schedule flexibility may be required

Nice To Haves

  • Associate or bachelor’s degree preferred (Business, Science, or technical field)
  • Experience with batch record review and documentation processes preferred
  • Knowledge of GMP and FDA regulations (preferred)
  • Proficiency with enterprise systems (SAP, LIMS, document management systems) preferred

Responsibilities

  • Provide administrative and operational support across multiple functions
  • Review batch records and documentation for accuracy and compliance
  • Ensure adherence to GMP and regulatory requirements
  • Serve as liaison between Production, QA, and cross-functional teams
  • Manage document control processes and tracking systems
  • Support inventory coordination and compliance activities
  • Maintain detailed records and reporting systems
  • Drive accuracy and quality in all documentation processes

Benefits

  • Excellent Benefits Package
  • Medical, Dental, & Vision benefits-effective Day 1
  • Paid Time Off & Holidays
  • 401K Company Match up to 5%
  • Tuition Reimbursement – eligible after 90 days!
  • Employee Referral Bonus
  • Employee Discount Program
  • Recognition Program
  • Charitable Gift Matching
  • Company Paid Parental Leave
  • Career Advancement Opportunities
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