QC Microbiology Associate II – cGMP Lab Ops

RXinsider LTD.

Marlborough (MA)

On-site

USD 32,000 - 101,000

Full time

13 days ago

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Benefits offered by this job

Healthcare
Well-being programs
Family planning benefits
Paid time off
Savings & investments
Location-specific perks

Job summary

Moderna is seeking a candidate based at our Marlborough, MA site to support cGMP microbiology methods for QC raw materials, plasmid, drug substance, stability, and finished product testing for mRNA products, plus environmental and critical utilities monitoring.

You will contribute to non-testing projects and activities as needed, including document certification and monthly biosafety cabinet cleaning, while working a 10-h shift in a collaborative and fast-paced environment dedicated to advancing

Qualifications

  • BS in a relevant scientific discipline with 0–2 years (or MS with 1 year) QC experience in a cGMP environment.
  • Excellent troubleshooting and ability to communicate issues clearly.
  • Familiarity with electronic databases (LIMS, SAP, LMS or equivalent).
  • Strong written and oral communication, and organizational skills.

Responsibilities

  • Execute compendial microbiological testing and other methodologies as needed.
  • Perform methods such as Endotoxin, Bioburden, Environmental Monitoring, Microbial identification, Culture Purity.
  • Support testing for in-process samples, drug substance, and drug product for clinical studies.
  • Assist in development, implementation, and maintenance of laboratory systems in accordance with cGMP requirements.
  • Perform general lab support activities including reagent prep, equipment maintenance, and cleaning of biosafety cabinets.

Skills

Troubleshooting
Communication
Project prioritization
Scientific knowledge
Documentation

Education

BS in a relevant scientific discipline
MS in a relevant scientific discipline

Tools

LIMS
SAP
LMS

Job description

Moderna is seeking a candidate based at our Marlborough, MA site to support cGMP microbiology methods for QC raw materials, plasmid, drug substance, stability, and finished product testing for mRNA products, plus environmental and critical utilities monitoring.

You will contribute to non-testing projects and activities as needed, including document certification and monthly biosafety cabinet cleaning, while working a 10-h shift in a collaborative and fast-paced environment dedicated to advancing

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