About Our Opportunity
We are a service provider collaborating with organizations worldwide for over 25 years.
Job Overview
This role will support our Pharmaceutical Manufacturing Operations and Technical groups to:
* Manage document revisions and ensure timely approval
* Develop and improve facility/process procedures and business processes
* Create and update Manufacturing Batch Records
* Design and generate Operations Area Logbooks
* Produce and update Training Documentation
* Enhance EH&S systems and documentation
* Design and generate PQ Protocols
* Improve other documentations associated with large molecule manufacturing
* Manage documents in our site documentation management system in line with our quality assurance program and standard operating procedures
Key Responsibilities
Some of the key responsibilities include supporting a dynamic Large Molecule manufacturing environment, developing a key understanding of core manufacturing principles, involvement in New Product Introductions (NPI), and delivering innovative results in various manufacturing functions.
Requirements
* Relevant engineering/science qualification or operational experience
* Masters 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
* Self-motivated/proactive approach with the ability to operate without close supervision
* Problem-solving skills and commitment to meeting deadlines
* 'Right first time' attitude and demonstrated technical writing skills
* Good planning and organization skills essential
We value diversity and equality, and recognize the collective strength found in the diverse backgrounds, skills, and experiences of our team members.