
Technical Writer - Pharma
- Cork
- Permanent
- Full-time
- Own document revision and routing on document management system and drive on time approval
- Design, update and improve facility/process procedures and business processes.
- Design, update and improve Manufacturing Batch Records.
- Design, generate and update Operations Area Logbooks
- Design, generate and update Training Documentation
- Design, update and improve EH&S systems and documentation.
- Design and generate PQ Protocols
- Design update/improve other documentations associated with the large molecule business.
- Managing documents in the site documentation management system in line with the site quality assurance program and local standard operating procedures.
- Support a dynamic Large Molecule manufacturing environment.
- Develop/learn key understanding of core manufacturing principles.
- Involvement in New Product Introductions (NPI).
- Deliver in innovative Manufacturing Areas.
- Support multiple manufacturing functions (Eng, Chemistry, QA, EHS, Micro)
- Relevant engineering/ science 3rd level qualification or operational experience
- Master's in engineering / science is desirable
- Previous pharma production, operations/ projects/process experience
- Strong sense of customer focus and teamwork
- Previously demonstrated flexibility and willingness to take on different job tasks
- Self-motivated/ proactive approach with the ability to operate without close supervision
- Proven ability to deal with unexpected issues using problem solving skills
- Commitment to meet deadlines
- 'Right first time' attitude.
- Demonstrated technical writing skills in the generation of documents and high level of IT skills
- Good planning and organisation skills essential