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PRODUCT RELEASE SPECIALIST/ Quality Control; Medical Devices

Job Title: PRODUCT RELEASE SPECIALIST/ Quality Control; Medical Devices
Contract Type: Contract
Location: Keighley, West Yorkshire
Industry:
Salary: £20000 - £22000 per annum
Reference: J904323_1579270456
Contact Name: Tom Hammond
Contact Email: tom.hammond@russell-taylor.co.uk
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.

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