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F

Quality Control Assistant

Frontline Recruitment Group Rothley
28,000 to 29,200
32 - 40 hour


Show Recently closed jobs

    F

    Quality Control Assistant

    Frontline Recruitment Group Rothley
    28,000 to 29,200
    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
    £28,000 to £29,200
    Hours
    32 to 40 hours per week
    Employment type
    permanent

    Job description

    Frontline Recruitment Derby are currently recruiting for a Quality Control Assistant to join our reputable client's Quality team based in Leicestershire, LE7.

    This is an excellent opportunity for someone with experience in quality control, manufacturing, pharmaceutical, food production or another highly regulated environment, who is looking to develop their career within a quality-focused role.

    About the Role

    Reporting to the Quality Manager, you will play an important role in ensuring that products meet the required quality, safety and regulatory standards before they are released.

    You will carry out routine and random quality checks throughout the production process, review documentation and certificates, and complete final product inspections to ensure that finished goods are fully compliant ready for dispatch. You will be working closely with both the production department and personnel ensuring they too meet the required standards in both their duties and their own PPE/Hygiene standards.

    Key Responsibilities

    Carry out random quality checks within production areas, checking works orders, stock and production processes against established quality procedures.

    Complete final production checks at the end of the manufacturing process before products are released to market.

    Review works orders and production instructions to ensure processes have been followed correctly.

    Build and maintain works orders using the ERP system.

    Obtain, review and file batch certificates for production batches.

    Review and verify Certificates of Analysis (COAs) for raw materials, packaging and finished products.

    Ensure 100% of batch documentation is complete, accurate and correctly filed.

    Ensure all required documentation meets internal procedures and relevant regulatory standards.

    Complete final checks on 100% of finished products prior to release.

    Identify discrepancies, quality issues or areas for improvement and communicate findings to the relevant departments.

    Work closely with Production, Operations, Planning, Purchasing, Maintenance and Quality teams to maintain high standards.

    Contribute to a culture of continuous improvement, compliance and quality excellence.

    What We're Looking For

    Essential:

    * Good understanding of Quality Control processes and procedures.

    * Knowledge of GMP (Good Manufacturing Practice), GDP (Good Distribution Practice) and other relevant regulatory standards.

    * Experience carrying out detailed and accurate inspections and quality checks.

    * Ability to review works orders, production documentation, packaging materials and finished products.

    * Experience reviewing and verifying Certificates of Analysis (COAs).

    * Strong attention to detail with a methodical and accurate approach to documentation.

    * Good written and verbal communication skills.

    * Ability to identify and report discrepancies and quality issues.

    * Strong team-working skills, with the ability to work effectively alongside Production, Technical and Quality departments.

    Desirable:

    Previous Quality Control experience within pharmaceutical, food manufacturing or another highly regulated manufacturing environment.

    Knowledge of Root Cause Analysis, CAPA or Fishbone analysis.

    Understanding of workplace health and safety requirements within a manufacturing environment.

    Experience working within an ERP system.

    Why Apply?

    This is a key role within the Quality function of a leading pharma company, helping to ensure products are manufactured correctly, documentation is accurate and complete, and finished goods meet the required standards before release.

    You will work alongside a range of departments and have the opportunity to develop your knowledge and experience within a structured and quality-driven manufacturing environment.

    The client is committed to:

    * Continually improving

    * Enjoying working together, on the same side

    * Having integrity in everything they do!

    Hours of work: Some flexibility in start times so either 7-3 pm or 8 - 4 pm Monday to Friday (37.5 Hour week)

    Salary: Up to £15 ph, overtime at enhanced rates plus company benefits,

    If you have a strong eye for detail, take pride in getting things right and have experience within a quality-controlled or regulated environment, we would love to hear from you
    Salary description

    £28000.00 - £29200.00 per year

    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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