Laboratory GMP Compliance Coordinator

Thermo Fisher Scientific•New Brunswick, NJ
•$25 - $31•Onsite

About The Position

This is a fully onsite role based at our customer’s site in New Brunswick, NJ. Thermo Fisher Scientific is a leading global contract research organization and world leader in serving science, passionate about enabling customers to make the world healthier, safer, and cleaner. Our Laboratories Functional Service Partnership (FSP) team advances drug development by creating sustained groups of talent within customer organizations. This collaborative approach brings professionals with commitment to excellence, industry knowledge, and operational strength directly into customer environments to enhance capabilities and advance the delivery of life-changing therapies.

Requirements

  • Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’)
  • Experience working in GMP environment- either laboratory setting, manufacturing, or quality/compliance.
  • Must be legally authorized to work in the United States without sponsorship.
  • Must be able to pass a comprehensive background check, which includes a drug screening.
  • Proficient in Microsoft outlook, word, excel, MS team meetings, SharePoint, Learning Management Systems (LMS), Electronic Document Management Systems (EDMS).
  • Able to conduct video conference calls via MS teams 4-6 hours a day with team members at different sites. (flexibility for early AM meetings/calls due to time zones)

Nice To Haves

  • Experience in GMP training management and/or GMP documentation is preferred
  • Writing and reviewing standard operating procedures, experience with change control and deviations/investigation is a plus.
  • Demonstrated ability to successfully manage competing deadlines and balance priorities.
  • Excellent technical writing skills, close attention to detail and excellent follow up.
  • In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Responsibilities

  • Support all aspects of the Documentation and Training Management program for GMP laboratories and supporting functions that support clinical manufacturing.
  • Responsible for ensuring compliance with company requirements for GMP Documentation and Training Management.
  • Manage daily service requests for all training related updates in the Learning Management System.
  • Escalate training related issues promptly and follow through until resolved.
  • Create and maintain training curricula, and training items.
  • Create and manage new hire Learning Plans in collaboration with hiring managers.
  • Support authoring of Documentation and Training content.
  • Manage training impact assessments for standard operating procedures (SOPs).
  • Manage training related documentation and approval workflows in the Electronic Document Management Systems (EDMS).
  • Manage scanning, uploading, and indexing of any paper documentation to the EDMS or submission to documentation storage facility.
  • Support documentation and training compliance requests for laboratory audits and inspections.
  • Calculate department training compliance metrics and communicate to management.
  • Work independently but recognize need to consult stakeholders and keep them informed of progress.
  • A self-starter with an ability to manage electronic systems, MS outlook and office with minimal training and supervision.

Benefits

  • Competitive remuneration
  • Annual incentive plan bonus
  • Healthcare
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO)
  • 10 paid holidays annually
  • Paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave)
  • Accident and life insurance
  • Short- and long-term disability
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
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