QA Specialist
CK Science
Montrose, Scotland
13d ago
  • Salary : Up to £17.40 per hour
  • REF Number : 00045066
  • Consultant : Abbi Carmody
  • Sector : Pharmaceutical
  • Discipline : Qa / Validation
  • CK Group is recruiting for a QA Specialist to join a company in the Pharmaceutical industry at their site based in Montrose on an initial 12 month contract basis.

    Our client is a global healthcare company who take on some of the world's biggest healthcare challenges. By delivering a sustainable business, they provide health benefits to patients and consumers.

    They have three world-leading businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.

    They are committed to widening access to their products, so more people can benefit, no matter where they live in the world or what they can afford to pay.

    The Location :

    The site is a 45-acre primary manufacturing site by the sea with over 300 permanent staff on-site. At this site Active Pharmaceutical Ingredients are converted into tablets, creams, and inhalers used for the treatment of Asthma, Eczema, AIDS / HIV, Influenza, high blood pressure plus more.

    The site is situated 38 miles north of Dundee between the mouths of the North and South Esk rivers.

    The Role :

    The QA Specialist will drive improvements in GMP and quality system compliance across the site by providing guidance, support and training to Montrose Site.

    To provide metrics, manage and develop Site Quality Systems : Deviation Process CAPA Process Internal Audit Program QIR process Documentation control process Change control process

    Key Duties :

  • Manage the Document control.
  • Manage the internal audit process.
  • Ensure departments compliance to record retention policy.
  • Management of legacy validation documentation.
  • Manage the key Quality Processes such as Change Control.
  • Your Background :

    To succeed in this role you will have worked in a similar role and have experience in quality management within the pharmaceutical industry.

    Excellent communication and IT (SAP) skills. Knowledge of CAPA's, validation and GMP.

    Step 2
    Add to favorites
    Remove from favorites
    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Application form