Quality Control Analyst, I

Cambridge, Massachusetts

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Type: Contract

Experience: 0

Category: Scientific & Clinical

Contractor Work Model: Onsite

Brand: Joulé

Compensation Range: 32.00 - 38.00 Per Hour

Job ID: 346606

Date Posted: 02/19/2026

Shortcut: http://jobs.systemone.com/Kg966g


Title: Quality Control Analyst, I
Location: Cambridge MA moving to Burlington MA
Duration: 6 month contract to hire
Start: ASAP
Schedule: Monday thru Friday (flex start) 40 hour work week
Salary: $32 to $38/hr based on experience



Education:
BS plus 0-2 years’ industry experience in cGMP lab environment, OR AS, 2-4 years’ industry experience OR
HS Diploma, 4+ years’ industry experience in cGMP lab environment, or equivalent

Qualification:
Basic working knowledge of cGMP regulations and/or lab experience

Preferred Qualifications:
1 year of experience in a cGMP lab environment.
Proficient in Outlook, MS Word, Excel and lab based data management systems (LIMs).
Experience with microbiological testing or environmental monitoring

Experience in biotech, pharmaceutical or other regulated industry

Responsibilities:

  • Perform routine QC testing for raw materials, in-process, DP, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, plate reader, etc. in accordance with SOPs and cGMP guidelines.
  • Perform cell culture microbial and/or molecular assays.
  • Perform routine Environmental Monitoring and utilities testing.
  • Perform microbial limits, Bioburden testing, and identifying and trending microorganisms.
  • Lab support including but not limited to glass washing, autoclaving, etc.
  • Assist in the review of QC data and provide summaries to management as needed.
  • Report out-of-specification or out-of-trend results in a timely manner to ensure appropriate actions are taken.
  • Performance of QC general laboratory equipment calibration and maintenance, laboratory housekeeping and preparation of the laboratory for audits.
  • Participate in transfer methods from support groups to the QC laboratory.
  • Coordinate departmental systems (i.e. inventory, documentation, equipment maintenance).
  • Author and conduct periodic review to QC documents, including SOPs, protocols and forms as needed.
  • Initiate deviations and lab investigations as needed.


#MS558


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