Quality Control Analyst

Norton, MA, US • Posted 4 days ago • Updated 10 hours ago
Full Time
On-site
USD $40.00 - 45.00 per hour
Fitment

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Job Details

Skills

  • Training
  • HPLC
  • GLP
  • Inventory
  • Test Methods
  • Continuous Improvement
  • Auditing
  • Biology
  • Biochemistry
  • Pharmaceutics
  • Analytical Skill
  • Testing
  • LIMS
  • Data Analysis
  • Documentation
  • Technical Writing
  • Aseptic Technique
  • Chemistry
  • Microbiology
  • Attention To Detail
  • Insurance
  • Quality Control
  • GMP
  • Regulatory Compliance
  • FOCUS

Summary

Quality Control Analyst


Location: Norton, MA (Onsite)


Pay: $40-$45/hr.


Schedule: Friday-Monday, 4x10 (Weekend Coverage)


Shift: 1st Shift (Training Mon-Fri initially)

We are seeking a Quality Control Operations (QCO) Analyst II to support GMP-compliant laboratory operations in a regulated biotech environment. This role focuses on analytical and microbiological testing, data review, and supporting QC lab operations from development through commercialization.

Key Responsibilities:


  • Perform routine and non-routine analytical (HPLC/UPLC) and/or microbiological testing for raw materials, in-process, release, and stability samples

  • Conduct bioburden, endotoxin, environmental monitoring, and aseptic technique-based testing (microbiology-focused work preferred)

  • Support weekend QC lab operations and ensure compliance with GMP/GLP standards

  • Assist with method transfers, validation, verification, and implementation activities

  • Review and qualify analytical data in a timely manner

  • Maintain lab readiness, including reagent prep, inventory, and equipment support

  • Contribute to SOPs, controlled documents, and test method updates

  • Support investigations, data trending, and continuous improvement initiatives

  • Participate in audits, inspections, and regulatory readiness activities


Qualifications:


  • B.S. in Chemistry, Biology, Biochemistry, or related scientific field

  • 4-8 years of experience in GMP QC or biotech/pharmaceutical laboratory environments

  • Strong experience in microbiology (preferred) and/or analytical testing

  • Familiarity with GMP standards and controlled laboratory environments required

  • Experience with LabWare LIMS strongly preferred

  • Strong data analysis, documentation, and technical writing skills


Ideal Candidate Profile:


  • 4-5 years of GMP lab experience (mid-level, not entry or senior)

  • Background in bioburden, endotoxin, environmental monitoring, aseptic technique

  • Chemistry + microbiology blend preferred

  • Strong attention to detail and ability to work in a structured, regulated environment


Employee Benefits


  • Medical, dental, vision, and pet insurance

  • 401(k) Retirement Savings Plans

  • Employee Assistance Program (EAP)

  • Commuter/Parking Accounts

  • People Perks

  • Health Savings Account (HSA)

  • AD & D Insurance


This role is best suited for a QC professional seeking hands-on laboratory work in a fast-paced GMP weekend schedule with a strong compliance focus.

Click "Apply Now" to be considered.



The base pay range listed reflects what we reasonably expect to offer for this role. Actual pay may vary based on location, experience, and performance. Depending on the position, benefits may include medical, dental, and vision coverage; retirement and savings plans; paid holidays and time off; supplemental insurance; and additional wellness or incentive programs.



About Us

Advantage Technical connects top- talent in technology, engineering, and technical fields with forward-looking companies.


Advantage Technical is an equal opportunity employer. All applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other legally protected status. Advantage Technical offers reasonable accommodations for qualified individuals with disabilities; contact your local branch for inquiries. Advantage Technical is an E-Verify employer. See our Privacy Notice for Candidates and Employees/Contractors at By applying, you consent to receive AI-generated and non-AI-generated calls, texts, or emails from Staffmark Group, its affiliates, and partners. Frequency varies and message/data rates may apply. Reply STOP to cancel or HELP for help.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10118370
  • Position Id: 2015386
  • Posted 4 days ago
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