
Biopharmaceutical Documentation Specialist
20 hours ago
Job Opportunity
We are seeking a highly skilled Technical Document Specialist to join our team in Cork, Ireland. This is an excellent chance to work with a leading Biopharmaceutical company that focuses on creating life-changing products.
The successful candidate will be responsible for creating and updating documentation, Standard Operating Procedures (SOPs), Business Processes Documents (BPDs), Protocols, Reports, Work Instructions (WI) etc. in a compliant manner.
Main Responsibilities:
- Work independently to create and update technical documents.
- Evaluate and create/update SOPs, BPDs, Protocols, Reports, WI etc. in a compliant manner.
- Publish SOPs through VEEVA compliance system.
- Collaborate with relevant teams, Labs, Quality etc.
Key Skills and Qualifications:
- Previous experience with VEEVA is essential.
- Strong technical writing background is required.
- Ability to work independently and collaboratively with cross-functional teams.
- Good attention to detail and ability to gather data, develop reports and track feedback.
- Strong technical understanding of biopharmaceutical industry.
Benefits:
- This role offers the opportunity to work in a state-of-the-art facility.
- Contribute to creating life-changing products.
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