Job Title: Document Controller
About the Project:
The Document Controller will be responsible for maintaining and controlling engineering documentation at a biopharmaceutical manufacturing site in Cork. The team on site grows, purifies, formulates, and bulk fills mammalian cell culture derived APIs for medicines intended for human use.
* 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:
We are seeking a highly organized and detail-oriented individual with a degree in sciences, engineering or equivalent. The ideal candidate will have at least 3 years of experience in Document Control or a related function such as Engineering, in a global Pharmaceutical and/or Biotechnology Company.
* 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
* Proficient with computer and standard software programs
* Stamp 1G or Stamp 4 visa required for applicants interested in contracting opportunities within the pharmaceutical sector in Ireland