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Senior Quality Control Analyst

Contract · In Office · Portsmouth, New Hampshire (USA)

$51,000–$69,000 · Posted Aug 17, 2026

Work Options
Seniority Level
Job Type
Position Group
  • Now Hiring: QC Analyst III / IV
  • Location: Portsmouth, NH – 101 International Drive
  • Contract: 6 Months | Potential Extension or Full-Time Conversion
  • Pay Rate: $51.09–$69.34/hour (W2)
  • Benefits: Weekly Pay | Medical | Dental | Vision Insurance
  • Position Overview
  • We are seeking an experienced QC Analyst to join a Quality Control team supporting analytical testing, product release, stability studies, investigations, and continuous improvement within a cGMP-regulated pharmaceutical/biopharmaceutical environment.
  • The ideal candidate will have strong hands-on experience with HPLC/UPLC, electrophoresis, analytical instrumentation, laboratory investigations, data integrity, and quality systems, along with the ability to mentor junior analysts and support cross-functional teams.
  • Key Responsibilities
  • • Perform and review analytical testing using HPLC/UPLC, electrophoresis, spectrophotometry, and other analytical techniques
  • • Support in-process and final product testing and stability studies
  • • Troubleshoot laboratory instruments, software, and analytical processes
  • • Support deviations, investigations, change controls, and continuous improvement initiatives
  • • Coordinate equipment maintenance, calibration, and vendor activities
  • • Support audit readiness and regulatory/customer inspections
  • • Provide technical guidance, training, and mentorship to junior QC analysts
  • • Collaborate with Manufacturing, QA, MSAT, PV, and other cross-functional teams
  • • Ensure compliance with cGMP, SOPs, data integrity, and laboratory safety requirements
  • Required Qualifications
  • • Bachelor's degree in Biochemistry, Chemistry, Biology, or related scientific discipline
  • • 5–10 years of relevant industry experience
  • • Experience in QC laboratory operations and analytical testing
  • • Strong understanding of cGMP and data integrity
  • • Experience with laboratory investigations, documentation, troubleshooting, and quality systems
  • • Hands-on experience with HPLC and/or UPLC
  • Preferred Experience
  • • Stability testing and commercial/clinical manufacturing support
  • • Capillary electrophoresis, icIEF, PCR, or spectrophotometry
  • • QC/Laboratory SME experience during audits
  • • Training or mentoring junior analysts
  • • Continuous improvement, 6S, change controls, and process optimization
  • Key Technologies
  • HPLC | UPLC | Capillary Electrophoresis | icIEF | PCR | Spectrophotometry | SoloVPE | Cary 60 | PA-800 | ProteinSimple iCE3 | KingFisher Flex | Sysmex CS-2500

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Senior Quality Control Analyst

Tailored Management

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