Technical Writer (BBBH28339) Cork, Republic of Ireland
LSC has a great contract opportunity for a Technical Writer 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 grows, purifies, formulates, and bulk fills mammalian cell culture derived APIs for medicines intended for human use.
If you have 2 years of experience in a GMP regulated environment and are ready for your next challenge, this could be the perfect project for you!
About the Project - Key Responsibilities:
1. Manage the authoring and drafting of all types of External Quality documentation.
2. Support document updates and manage timelines for cross-functional projects.
3. Act as a SME/Superuser on the Controlled Document System to facilitate the processing and approval of documents.
4. Organize and facilitate Document Round Table meetings with cross-functional teams as required.
5. Support quality metric management for external quality and partner teams.
6. Coach and train colleagues in Documentation System and GDP queries.
About You - Are Your Skills a Match?
* 2+ years of experience in technical writing.
* Proficient in data analytics and data visualization.
* Working knowledge of Regulations, GMP, and GDP.
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or Stamp 4 visa. Please note we are unable to provide visa sponsorship. Thank you for your understanding.
Apply via this advert or contact Sarina Abdulha at LSC on 021-4777329 if you have any questions about this opportunity!
Application Details
Name: (Please include your first and last name)
Email: (Please include your email address)
Phone: (Please include your country code)
CV / Resume: (Please attach your CV)
Eligibility to work: (Yes, I am currently eligible to work in the country I am applying to / No, I am not currently eligible)
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