QC Associate II

Found in: Appcast Linkedin GBL C2 - 3 weeks ago

Norwood, United States Randstad Life Sciences US Full time

6 Month Contract

Norwood, MA

PR: $25-34/hour


Shifts:

2nd shift = 2pm-12am, Wednesday-Saturday (15% shift differential)

OR

2nd shift = 2nd Shift, 2pm - 12am Sun-Wed (15% shift differential)

OR

3rd shift = 10pm-8am, Wednesday-Saturday (25% shift differential)


Job Summary

Seeking a contract role in Quality Control Sample Management Associate II based at their Norwood, MA site. The individual in this role will perform cGMP QC sample management activities for QC Chemistry, Microbiology, Bioassay, and various Development labs.


Job Responsibilities

  • Sample coordination including cross functional collaboration with internal and external labs
  • Receipt, processing, distribution and shipment of the following sample types:
  • In-Process, DS, Formulation and DP
  • Equipment cleaning
  • Stability
  • Raw Materials
  • Coordinating domestic and international sample shipments
  • Communication with external Contract Test Labs (CTLs)
  • Interact with Development teams in a GMP compliant manner
  • Inspect product and raw material retention samples
  • LIMS (LabVantage) sample logging and result entry
  • AQL visual inspection of drug product
  • Stability program support
  • Controlled temperature unit management, maintenance and troubleshooting
  • Clean room gowning
  • Managing/stocking of QC lab supplies
  • Write/revise SOPs, protocols and reports
  • Complete and maintain cGMP documentation for work performed
  • Participate in authoring quality systems records such as deviations, change controls, CAPAs.
  • Support non-conformance investigations
  • Establish and maintain a safe laboratory working environment
  • This position will support first shift QC Sample Management operations at Moderna, Wednesday through Saturday
  • Additional duties as may be assigned from time to time


Education & Qualifications

  • Education: Bachelor’s degree in a relevant scientific discipline
  • Experience: At least two years in a cGMP laboratory setting
  • Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations.
  • General laboratory operations (Pipette and analytical balance use.)
  • Strong technical writing skill
  • Proficiency with Microsoft Office Programs
  • Quick learner with electronic databases (e.g. LIMS, SAP, LMS)
  • Strong written and oral communication skills as well as organizational skills
  • General knowledge of industry standards and guidelines for quality control laboratory operation
  • Demonstrated ability to work effectively under established guidelines and instructions
  • Ability to collaborate effectively in a dynamic, cross-functional matrix environment.
  • Be able to follow the relevant Standard Operation Procedures as written.
  • Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.
  • A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

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