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QA/OQ Manager position – High end pharmaceutical client in the North East of England!

Location: NORTH EAST ENGLAND, ENGLAND Salary: Salary Negotiable
Sector: Scientific Job Type: Permanent
Shift Type: N/A Applications: N/A
Posted: 2 months ago Reference: 3112422
Have you been a quality lead in the life science or pharmaceutical sector? Do you have experience of project management in production in the pharmaceutical or fine chemical manufacturing sector? My client are recruiting into a permanent role at their site based in the North East of England.

Your day to day responsibilities will be:
• Performance of batch activities (reviews/approvals/audits) relating to pharmaceutical and chemical products.
• To maintain the existing quality management systems in line with relevant quality standards and regulations.
• The performance of OQ duties including change controls on product registrations.
• Co-ordination of validation activities.

You will be right for the role with the following background:
• A degree in a Science (or equivalent, relevant experience).
• 5 or more years of relevant experience in a GMP pharmaceutical production environment.
• Proven ability to maintain quality systems.
• Experience of cGMP regulatory inspections.
• Experience working as part of a multi-discipline team with an appreciation for the commercial aspects of project delivery.

Candidates with a strong background will excel in this role which is seeking candidates to start as soon as possible!

Tell me how you are suitable for the role and send your CV in Word format to paul.mears@reedglobal.com (2 pages maximum, Word document format) by Friday 27th October as the prospects of the role at this leading pharmaceutical company will attract the most desirable candidates in the field.