Tech Writer
Job Description
Supporting Pharmaceutical Manufacturing Operations and Technical groups to;
· 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.
Opportunity to:
· 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)
Requirements:
· 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