Quality , Science, Pharmaceutical & Food

QA Documentation/Admin Specialist

  • Contract
  • Remote
  • Dublin North
  • 41950718

PE Global are currently recruiting for a QA Documentation/Administration Specialist on behalf of our client based in Dublin:

11 Month initial contract

 

This role will be responsible for supporting the Quality Department in the management of the site GMP documentation, and in support of the Quality functions in various administrative duties. Ensure that objectives are effectively achieved, consistent with the company requirements to ensure compliance, safety and reliable supply to our customers

 

Key Responsibilities:

  • This position will include a combination of the responsibilities as follows:
  • Supporting the management of the site Documentation / SOP management systems
  • Provides compliance contribution to project teams and leads specific projects.
  • Understands and applies regulatory / compliance requirements to their role together with remaining current on upcoming regulatory and compliance changes.
  • Responds to non-standard requests from customer needs.
  • Makes decisions within guidelines and policies which impact own priorities and allocation of time to meet deadlines.
  • Use standard systems including MS Word, Excel, PowerPoint, Outlook, SAP and various company and industry specific software such as document tracking, work order entry/tracking, procurement, manufacturing entry/reporting, etc.
  • Presentation, compilation and review of data as directed
  • Act as Assistant to Head of Department (part time) with associated diary management activities
  • Scheduling, coordinating and monitoring appointments for department managers and Leads
  • Management of purchase orders and associated activities related to budgets
  • Monitoring of department training due dates in Learning Management System (LMS)

 

Key Experience:

  • A minimum of 1-2 years experience in Quality Control, Quality Assurance or Pharmaceutical or Biological Operations
  • Knowledge of EU/US quality related pharmaceutical regulations
  • Basic computer literacy
  • Strong communication skills
  • High level of technical aptitude & motivation
  • Demonstrated initiative and pays attention to detail
  • Good presentation skills.
  • Excellent knowledge of relevant Quality and GMP Compliance Guidelines

 

Education:

Bachelor’s degree (or higher) in Chemistry, Biology, Microbiology, Automation, Engineering or equivalent

 

 

Interested candidates should submit an updated CV.

 

Please click the link below to apply, call Audrey on 0214297900 or alternatively send an up to date CV to audrey.mccarthy@peglobal.net

 

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

 

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