R&D Quality Administrator

Job Ref: J32269
Sector: Science
Sub-sectors: Biotech/Life Sciences, Pharmaceuticals, Medical Devices
Job Type: Permanent
Date Added: 10 June 2019
  • Halewood, Merseyside, England, UK Halewood Merseyside UK L24 8RB
  • Competitive
    ANNUM
  • Behruz Sheikh
  • 0161 868 2202
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An opportunity for a Quality Administrator/Document Controller to move into an international Biopharmaceutical company.

R&D Quality Administrator II Permanent North West England

I am currently working with a global Biopharmaceutical company who are looking to recruit a R&D Quality Administrator into their Quality Assurance team. The company have a portfolio of innovative leading brands spanning from eye care and dermatology to regenerative products with this site in North West England being their R&D site with a drive to innovate and develop even more.

This is the perfect opportunity for anyone with quality documentation experience within a ISO/GMP setting to move into a R&D Biopharma company into their QA team. The role will be fast paced and involve the movement from paper based documentation to electronic systems.

Benefits -8% bonus -10% contributory pension -Flexible working hours

Requirements: The successful candidate should have industry experience of working with Quality Documentation within a regulated industry e.g. cGMP, ISO 13485. They should have good knowledge of; writing SOP's, quality system applications, compliance documents and archived documentation.

If you would like to register your interest for this position and get further information, please use the link provided. Else please email a copy of your CV to Tyler Datlen at Tyler.Datlen@srg.co.uk.

If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit www.srg.co.uk to view our other vacancies. SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

Keywords: GMP, cGMP, ISO 13485, documentation, QA, QAO, SOP, batch documentation, logbook, QMS, quality management systems, master files, audit, document control, quality administrator, quality assurance, archive, medical device, pharmaceutical, biopharmaceuticals

SRG
10/07/2019 15:24:13
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