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.
Apply via this advert or contact Grinne Hodnett at LSC on if you have any more questions about this opportunity!
Skills: Document Control GMP Engineering