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Temporary Manufacturing Personnel

Location: 
Boston
Date Posted: 
02/05/2020
Employment Type: 
Contract
Job ID: 
10620
Description: 

Job Summary

Responsible for daily GMP operations in the DPF, including the set-up, disassembly, and cleaning, and storage and organization of solid oral manufacturing process equipment.

Key Responsibilities include but are not limited to:

  • Excellent understanding of and strict adherence to cGMP requirements including:
    • Compliance with all on-going training requirements
    • Following SOPs, policies and all other relevant  work instructions to ensure the successful and compliance operation of the drug product facility
  • Interface with cleaning staff, Facilities/Operations, Quality, EH&S, Materials Management and the Release and Stability Lab to ensure facility operation
  • Manage storage and organization of equipment in the facility
  • Order consumables and ensure inventory

Educational Requirements

-    High School or Vocational School Diploma

Basic Qualifications (Min Requirements)

  • Ability to follow verbal and written instructions in English
  • Visual Acuity.
  • Ability to distinguish between the colors red, yellow, blue and green.
  • Ability to lift up to 50lbs.
  • Strong communication skills, as well as excellent documentation skills.
  • Organizational skills (5S or 6 sigma training preferred)
  • Basic computer skills and demonstrated ability to learn new systems and understand new technologies.
  • Experience in a GMP environment preferred