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