Product Release Quality Coordinator - West London

  • Salary: Up to £26 per hour Paye
  • REF Number: 00046016
  • Consultant: Julie Marshall
  • Contact: 01438 842964
  • Date Published: 09.07.2019
  • Sector: Pharmaceutical
  • Location: London, South East
  • Discipline: Qa/Validation

CK Group is recruiting for a Product Release Quality Coordinator to join a company in the pharmaceutical industry at their site based in Brentford on a contract basis for 12 months. Rate will be up to £26 an hour max. (PAYE) dependant on level of experience.

The Company:

Our client is a global healthcare company who take on some of the world's biggest healthcare challenges. They provide health benefits to patients and consumers and have three world-leading businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.

The Location:

Brentford is located at the confluence of the rivers Brent and Thames. The area is well served by public transport from central London, Waterloo station and surrounding areas.

The Role:

Key Responsibilities: To lead, prioritise and provide an effective Product Release Service which ensures that all products released for sale or further processing have a quality appropriate to their intended use i.e. comply with Company GMP standards, Product Quality Specifications and Regulatory requirements. Generate and review product related technical documents such as Product Quality Reviews and Quality Agreements. Collate and interpret data and information such as analytical results/trends, regulatory/validation/engineering information. Lead and direct investigative work into products failing to meet requisite standards (and regulatory issues). Develop and agree corrective actions arising from such incidents. Investigate and report product customer complaints. Lead deviation investigation clinics.

Your Background:

You will have either HNC, Degree in Chemistry or equivalent in a science subject. Candidates must have background in Quality Assurance, with knowledge of GMP (and regulatory) requirements and ideally with the following skills and experience: Ability to manage multiple activities concurrently as roles are within high volume, complex areas. Able to demonstrate clear, reliable & timely decision making skills. Demonstrated written and verbal communication skills. Ability to demonstrate leadership would be an advantage as depending on knowledge and experience, the individual may be required to lead a small shift team.

For more information or to apply for this position, please contact Julie on 01438 723500 or email pharmacontracts@ckagroup.co.uk. 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 46016 in all correspondence.

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