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Job ID :
Location :
US - Massachusetts - Andover
Job Description


Project Manager:

  • Coordinate new equipment installation from assessment of lab, utility needs and coordination of vendors
  • Review Pfizer needs and schedule vendors accordingly

Planner/Scheduler role:

  • Escort lab instrument service vendors to work sites and provide locally required trainings to such service vendors.
  • Perform lab asset inventory reconciliation activities in the computerized maintenance management system (CMMS) (EAMS).
  • Support the processing of work orders in the computerized maintenance management system (EAMS) as needed.
  • Provide compliance and quality system management support to help ensure the LIS group is audit ready every day.
  • Maintain a continuous improvement mindset, and identify LIS process improvement opportunities.
  • Provide CAD support for Global Operations upon request.
  • Maintain effective relationships with the customer base.
  • Comply with all company policies and procedures and adhere to company standards.
  • Maintain intermediate to high computer skills necessary to access CMMS work order system, update equipment history and access material inventory management system.
  • Communicate clearly, understand and acknowledge verbal instructions, and be able to read and interpret work from drawings, written work orders, sketches, blueprints, and technical manuals.
  • Understand customer requirements and coordinate interface with other teams for various support requirements.
  • Maintain professional and customer-oriented relationships with team members, internal and external customers and service providers, and building occupants
  • Comply with all company policies and procedures and adhere to company standards.
  • Perform other job-related duties and special projects as requested.


  • Matrix to the Andover LIS Lead
  • WRD Andover Research lines
  • External Lab Instrument Vendors
  • Global Supply/Manufacturing (who owns the R&D facilities at the Andover site)


  • Minimum of 5 to 10 years of experience in the pharmaceutical industry.
  • Previous experience with working in a cGxP environment is required.
  • Must have experience working with typical pharmaceutical R&D lab assets including but not limited to HPLC, GC, Mass Spec, Plate Readers, Plate Washers, PCR, Partical Counters, Tubidimeters, Centrifuges, Incubators, Spectrophotmeters, etc.)


  • Understanding of Pharmaceutical R&D operations.
  • Proficient in using computer applications inclusive of Microsoft Word, Excel, and Outlook.
  • Experience using a CMMS system such as EAMS.
  • Experience in managing assets in a CMMS system.
  • Understanding of quality systems and continuous improvement programs.


  • Sitting for prolonged periods working at computer station.
  • Able to walk considerable distances on any given day (supporting 5 separate buildings across the Andover site).

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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