Document Control Role Cork

Documentation Specialist

  • Posted Last Week
  • Cork
  • Contract
  • VAC-19237

LSC have a great contract opportunity for a Documentation Specialist to join a global Biopharmaceutical company in Cork.

If you have knowledge and experience of GMP, GDP and DI in a pharmaceutical environment and are ready for your next challenge, this could be the perfect project for you!

ABOUT THE PROJECT - KEY RESPONSIBILITIES:

  • Updating/deletion of documents through the MIDAS system.
  • Preparation of change control documentation on TrackWise System.
  • Tracking of GCM tasks on TrackWise System.
  • Processing of documentation through the Change Control System.
  • Regular updates to Tier boards with various metric information such as Incidents, Investigations, CAPAs, GCM tasks, EHS actions, Safety metrics, etc.
  • Generation and control of Purchase Orders on SAP.


ABOUT YOU - ARE YOUR SKILLS A MATCH?

  • Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation (e.g. Manufacturing, Quality, Engineering, Tech Services etc).
  • At least three years experience in the Pharmaceutical industry or a similar regulated environment.
  • Multi-tasking in a fast-paced project environment


Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!

Apply via this advert or contact Siobhan Cummins at LSC on 021-4777329 if you have anymore questions about this QA Rep opportunity!

This could be the perfect project for you! Apply online and we’ll be in contact shortly

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The benefits of contracting with LSC

  • Partners to the world’s top Life Science companies we offer you the best contract opportunities in the industry
  • 95% of LSC contracts are renewed letting you choose contracting as a long term career option
  • LSC’s Consultant Success Programme focuses on skills development & on-site support to help you achieve your career goals!

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