GMP Manufacturing Coordinator Thermo Fisher Scientific Lexington

Title Gmp Manufacturing Coordinator
Date 2020
Company Thermo Fisher Scientific
City Lexington

Short Description :

Supporting groups/vendors Facilities, Scheduling, Cleaning Contractors, etc Provides training to Employees and Contractors for gowning and disinfection, as well trainings required for access into the controlled facilities Work crossfunctionally with support groups such ,…

Full Description :

Job Title: MFG Suite Coordinator
Requisition ID: 114241BR
When you’re part of the team at , you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
Position Description/Summary
Responsible for working closely with Manufacturing and Scheduling Teams to support daily manufacturing operations.
Responsibilities include:

  • Responsible liaison between the Manufacturing group and other supporting groups/vendors (Facilities, Scheduling, Cleaning Contractors, etc.)
  • Provides training to Employees and Contractors for gowning and disinfection, as well trainings required for access into the controlled facilities.
  • Works with the scheduling team to assist in planning manufacturing activities, maintenance and calibration of equipment and instruments and maintaining schedule adherence
  • Prepares materials for manufacturing for both day-to-day and multiple-week outlook
  • Assist in organizing and maintaining inventory to support MFG activities
  • Work cross-functionally with support groups such as Facilities, Engineering, Contamination Control Teams, Quality Control and Quality Assurance
  • Follows verbal and written procedures; accurately completing appropriate documentation
  • Demonstrates ability to troubleshoot basic issues in relation to GDP
  • Ensure cleaning schedule and MFG schedule remain on track by completing and communicating timelines appropriately
  • Support Operations needs that may include but is not limited to ordering of supplies, and backorder reporting, etc.
  • Must be able to work in a fast-paced environment
  • Understands cGMP & GDP requirements
  • A strong attention to detail through a minimum of an 8-hour shift
  • Work towards solutions to given problems and operate under cGMP requirements
  • Qualify to work in aseptic environments to complete required production activities
  • Maintain facility and room inspection readiness
  • Ability to lift at least 50lbs
  • Ability to aseptically gown and/or sterile gown as needed
Work Hours: 8 hours Monday – Friday, may require some flexibility to accommodate vendor support. May require overtime, weekends or holidays, as required to support the site as needed
Additional Responsibilities:
  • Work in accordance with site and company EHS programs
  • Work in accordance with regulations, detailed protocols and SOP’s
  • Written communications may be required to relay activities being performed
Knowledge, Skill and Requirements
Minimum Qualifications:
  • High School diploma and 5-7 years’ industry related experience in cGMP manufacturing
  • Bachelor’s Degree 1-3 years

Preferred Qualifications:
  • The ability to effectively communicate in English and Spanish
  • Experience with SAP and inventory control
  • Skilled in Microsoft office applications

At , each one of our 65,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
Apply today!
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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