Posted: 28 August
Offer description
As a Technical Document Specialist, you will play a vital role in developing and maintaining our Pharmaceutical Manufacturing Operations and Technical groups.
* Develop facility/process procedures and business processes by designing and improving existing documentation.
* Design, generate and update Manufacturing Batch Records and Operations Area Logbooks.
* Create Training Documentation that meets site quality assurance program standards.
* Improve EH&S systems and documentation while designing PQ Protocols.
* Manage documents in the site documentation management system according to local standard operating procedures.
* A dynamic Large Molecule manufacturing environment.
* Key understanding of core manufacturing principles through development and learning.
* Involvement in New Product Introductions (NPI).
* Deliver results in innovative Manufacturing Areas.
* Support multiple manufacturing functions including 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 ability to operate without close supervision.
* Proven ability to deal with unexpected issues using problem solving skills.
* Commitment to meet deadlines.
* Demonstrated technical writing skills in the generation of documents and high level of IT skills.
* Good planning and organisation skills essential.
