Document Development Specialist
Skill in Document Management Systems and Strong Technical Writing Skills are essential for this role.
Key Responsibilities Include:
* 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.
Opportunities to Develop Key Understanding of Core Manufacturing Principles and Involvement in New Product Introductions (NPI).
The Ideal Candidate Will Have:
* A relevant engineering/science 3rd level qualification or operational experience.
* A master's in engineering/science is desirable.
* Previous pharma production, operations/projects/process experience.
* Strong customer focus and teamwork skills.
* Demonstrated flexibility and willingness to take on different job tasks.
* A self-motivated/proactive approach with ability to operate without close supervision.
* Proven problem-solving skills.
* Good planning and organisation skills essential.
This Role Offers a Chance to Work in a Dynamic Large Molecule Manufacturing Environment Supporting Multiple Functions Including Engineering, Chemistry, QA, EHS, Micro.