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L

Senior QC Reviewer / Planner

L M Manufacturing Limited Weedon Bec
34,000 to 36,000
32 - 40 hour


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    L

    Senior QC Reviewer / Planner

    L M Manufacturing Limited Weedon Bec
    34,000 to 36,000
    32 - 40 hour
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Salary
    £34,000 to £36,000
    Hours
    32 to 40 hours per week
    Employment type
    permanent

    Job description

    Senior QC Reviewer / Planner
    📍 Weedon, Northamptonshire (NN7 4PP)
    💷 £34,000 – £36,000 per annum (depending on experience)
    ⏰ Permanent | Full Time | Monday to Friday
    Benefits
    * 21 days annual leave plus UK bank holidays, with additional annual leave based on length of service (up to 4 extra days).
    * Statutory pension scheme, 7 days paid sick leave, Time Off in Lieu (TOIL) and free parking.
    * Stable long-term career opportunities and development support
    Looking for a secure role in pharmaceutical quality?
    Join LM Manufacturing as a Senior QC Reviewer / Planner supporting our Quality Control function.
    This role is suited to candidates with experience in analytical data review, laboratory planning and compliance within pharmaceutical or regulated laboratory environments.
    Key Responsibilities
    * Review analytical data generated from QC testing activities
    * Support planning and coordination of QC testing schedules
    * Review data from HPLC, UV, FTIR and Karl Fischer analysis
    * Support compliance with ALCOA++ principles, data integrity and GMP requirements
    * Assist with laboratory investigations including OOS, OOT and deviations
    * Review documentation in line with quality and regulatory standards
    * Support method validation and adherence to ICH and 21 CFR requirements
    * Work collaboratively across QC and wider site functions
    What We’re Looking For
    * 5–8 years’ experience in Quality Control review or laboratory support
    * Experience reviewing analytical data in pharmaceutical or regulated laboratories
    * Familiarity with Chromeleon or similar laboratory software desirable
    * Understanding of data integrity, GMP and compliance requirements
    * Strong attention to detail and documentation skills
    * Ability to support planning and prioritisation of QC activities
    Desirable
    * Experience with OOS/OOT investigations
    * Exposure to method validation activities
    * Degree in Chemistry, Pharmacy or related scientific discipline
    Why Join Us?
    * Competitive salary
    * Secure permanent employment
    * Supportive quality team
    * Opportunity to build your career in regulated pharmaceutical manufacturing
    Apply now to join our Quality team
    Salary description

    £34000.00 - £36000.00 per year

    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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    Weedon Bec England

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