Engineering Document Control Specialist (BBBH28048) Cork, Republic of Ireland
LSC have a great contract opportunity for a Document Controller to join a Cork based Biopharmaceutical company. The site manufactures low volume bulk API for Phase III clinical trials, initial product launch and long-term market support. The team on site grow, purify, formulate, and bulk fill mammalian cell culture derived APIs for medicines intended for human use.
If you have 3+ years of experience in Document Control within a GMP environment and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
* Control and maintenance of the Engineering Documentation Control Centre.
* Control, issuance and archiving of Project & Site Drawings.
* Control and issuance of the numbering system for Commissioning & Restart Documents.
* Prepare and draft controlled documents through Veeva and Trackwise.
* Ensuring compliance within Engineering for removal of documentation from the Engineering Documentation Control Centre.
* Control of Engineering documents and Vendor documents to and from the Engineering Documentation Control Centre.
ABOUT YOU - ARE YOUR SKILLS A MATCH
* BA/BS degree in sciences, engineering or equivalent.
* At least 3 years of experience in Document Control or a related function such as Engineering, in a global Pharmaceutical and/or Biotechnology Company.
* Outstanding interpersonal and communication (written and verbal) skills is required.
* Proficient with computer and standard software programs.
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please understand that we are unable to provide visa sponsorship. Thank you for your understanding.
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