QA Specialist - Montrose, Scotland

  • Salary: Up to £17.40 per hour
  • REF Number: 00045066
  • Consultant: Abbi Carmody
  • Contact:
  • Date Published: 25.03.2019
  • Sector: Pharmaceutical
  • Location: Northern Scotland
  • 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.

For more information or to apply for the QA Specialist position, please contact Abbi Carmody on 01246 457708 or Alternatively, please click on the link below to apply online now. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 45066 in all correspondence.

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