QC Analyst 3

Lenmar Consulting, Inc.

  • Portsmouth, NH
  • 27 days ago

    Highlights

    This is a senior-level position responsible for analytical testing, equipment troubleshooting, investigations, Data Integrity, and audit readiness, while also providing guidance to junior analysts. The QC Analyst IV will support in-process and final product testing, customer stability studies, and daily QC laboratory operations in a cGMP environment.

    Numbers & Facts

    LocationPortsmouth, NH

    Description

    Title: Senior QC Analyst – Analytical Testing
    Location: Portsmouth, NH (Onsite) 
    Duration: 8 Months Assignment with a Chance of Extension 
     

    Job Summary

    The QC Analyst IV will support in-process and final product testing, customer stability studies, and daily QC laboratory operations in a cGMP environment. This is a senior-level position responsible for analytical testing, equipment troubleshooting, investigations, Data Integrity, and audit readiness, while also providing guidance to junior analysts.


    Key Responsibilities:

    ·       Perform and review analytical QC assays for in-process and final products.

    ·       Support HPLC and Electrophoresis laboratory activities and advanced assays.

    ·       Troubleshoot laboratory equipment and software and coordinate maintenance/calibration activities.

    ·       Support investigations, change controls, work orders, and process improvements.

    ·       Maintain cGMP, Data Integrity, and laboratory compliance.

    ·       Support audit/inspection readiness and serve as a QC SME when needed.

    ·       Collaborate with Manufacturing, QA, MSAT, PV, and QC teams.

    ·       Provide guidance and feedback to junior analysts.

    ·       Complete assigned work accurately, independently, and on time.

     

    Required Qualifications & Skills:

    ·       Bachelor’s degree in Biochemistry or a related science field.

    ·       5–10 years of experience in QC/analytical laboratory functions.

    ·       Pharmaceutical/biopharmaceutical cGMP experience.

    ·       Strong hands-on experience with HPLC/UPLC and analytical testing.

    ·       Experience with assay execution and review.

    ·       Strong understanding of Data Integrity and quality compliance.

    ·       Experience with equipment troubleshooting, investigations, and audit readiness.

    ·       Strong data interpretation, problem-solving, written and verbal communication skills.

    ·       Ability to work independently with minimal supervision.

     

    Preferred / Additional Experience:

    ·       Agilent or Waters HPLC

    ·       Capillary Electrophoresis / PA-800

    ·       Protein Simple iCE3 / icIEF

    ·       SoloVPE / Cary 60

    ·       7500 Real-Time PCR

    ·       KingFisher Flex

    ·       Sysmex CS-2500

    ·       Immunology laboratory experience

    ·       Advanced assay execution/review

    ·       Experience mentoring or guiding junior analysts.

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