PRODUCT RELEASE SPECIALIST/ Quality Control; Medical Devices

Job Title: PRODUCT RELEASE SPECIALIST/ Quality Control; Medical Devices
Contract Type: Contract
Location: Keighley, West Yorkshire
Salary: £20000 - £22000 per annum
Reference: J904323_1579270456
Contact Name: Tom Hammond
Contact Email:
Job Published: January 17, 2020 14:14

Job Description

PRODUCT RELEASE SPECIALIST/ Quality Control; Medical Devices

Location: North Yorkshire

Type: FTC 12 months (has the potential to go permanent but not guaranteed)

Salary: upto £22,000 DOE (overtime available)

Additional Benefits: 3% 6% pension contribution, 25 days + BH holidays, share save scheme etc

Our Client, a leading Medical Devices company is looking to recruit for a Product Release Specialist who will work at their modern site in North Skipton; alongside working at this massive -impressive facility, this person will gain furthered career development working within a GMP, 13485 accredited QMS.

The Role:

Reporting to the Product Release Team Leader this person will:

Generation of certificates for export products & regulatory requirements

  • Generate batch reviews and release for various products across biocides & wound management, including sterile batch reviews.
  • Providing active support to operations for correcting paperwork in a timely manner.
  • Complying with site Health and Safety procedures at all times.
  • Ensuring compliance with company GDP policy and general GLP, cGMP principles.
  • Primary point of contact for batch release queries.
  • Liaising with other departments regarding priority release.
  • Assist in deviation investigations.
  • Documentation reviews and updates including those associated to periodic reviews
  • Generation of department metrics and monthly reports.
  • Acting as deputy for the Product Release Team Leader as required/ deputising if needed.
  • Working with Quality colleagues on improvement projects related to the role.
  • Taking ownership of Product Release processes.
  • Trainer - Competent to provide training in product release processes.

The Person:

  • Will ideally hold a Degree in a Scientific Discipline but not essential
  • Will have worked in a highly regulated environment in a Pharmaceutical, Contract Testing or Pharmaceutical setting (GMP, iso 13485, GDP any one of these)
  • Ideally will have SAP experience
  • 'Can do attitude', while maintaining outstanding attention to detail
  • Strong organizational skills are essential
  • Prioritization skills
  • Computer Literate (SAP, MRP, Excel, Outlook etc)
  • Ability to balance the need to work as an effective team member while proactively working on own initiative when required.

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k

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