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QA Document System Controller

Job Seekers Ireland Science Pharmaceutical

Job Summary

  • Dublin
  • Permanent
  • BBBH815224
  • May 09, 2022
  • Competitive
Job Description

I am currently seeking a Quality documentation system administrator to join a Dublin based pharmaceutical company on a 12month FTC.

This role has the opportunity to grow and expand internally in time based on performance and business needs. The primary purpose of this role is to manage and control validation and GMP documentation on site including SOPs, Artworks, QC Records, software change controls and provide general administrative support to the QA department.

For this role you will have 2 years' experience in a regulated pharmaceutical industry within a similar role. Extensive knowledge and experience of quality systems software's such as NextDocs desirable or any quality systems experience. Ability to work independently with strong organisational skills essential.

Responsibilities:

  • System administrator for NextDocs system.
  • Tracking SOP update and implementing new procedures.
  • Ensuring training is completed on systems.
  • Consulting with Artworks to ensure new packaging material specification and artworks are implemented.
  • Ensure documents are returned and filed.
  • Copying and distribution of HBP procedures
  • Complete administrative duties as needed.

If this role is of interest, please 'apply now.'

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.

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Consultant Details

Consultant Details

Aoife O'Driscoll
Aoife O'Driscoll
  • Senior Consultant | Engineering Recruitment
  • +353 (0) 21 2300300
  • aodriscoll@morganmckinley.com