Pilot Plant Project Coordinator
Full Job Posting
Location
- Macclesfield, UK Function: Chemical Development, PT&D
Make an impact through safe, efficient manufacturing
Are you a scientific or engineering professional who enjoys solving problems, improving processes and bringing different teams together?
As a Pilot Plant Project Co-ordinator , you’ll support the safe and compliant delivery of manufacturing and cleaning activities within our pilot plant.
Working closely with Campaign Managers/Technical Managers, Process Engineers and operational teams, you’ll co-ordinate plans, manage risks and identify opportunities to improve performance.
This is an opportunity to combine technical knowledge with practical project co-ordination in a highly collaborative clinical API manufacturing environment.
What you’ll do
In this role, you will:
Co-ordinate activities supporting COMAH critical task analysis across operations and engineering
Plan and organise critical task assessments, involve key stakeholders and manage associated documentation
Maintain operational metrics and process safety performance information
Align operational and engineering plans, keeping stakeholders informed of progress, risks and priorities
Work with Campaign Managers/Technical Managers to plan and deliver product changeover cleaning activities
Lead improvement activities aimed at reducing changeover times
Co-ordinate the ordering and management of materials required for cleaning and, where appropriate, manufacturing
Prepare relevant SHE and GMP documentation to allow execution of manufacturing and cleaning activities
Collaborate with Process Engineers on relevant engineering change controls
Lead or support investigations, problem-solving activities and deviation management
Share learning and encourage consistent working practices across the pilot plant
Essential experience and capabilities
You will need:
A degree or equivalent experience in a scientific or engineering discipline
Technical or engineering capability gained in a relevant environment
A data-led approach to evaluating process performance and identifying improvement opportunities
The ability to organise priorities and co-ordinate activity across different teams
Clear communication skills and the confidence to raise risks with key stakeholders
A collaborative approach and commitment to safety, quality and compliance
A background in chemistry or chemical engineering would be particularly relevant, although we welcome applicants with equivalent experience from other scientific or engineering disciplines.
Desirable experience
It would be helpful if you also have:
Experience of structured problem-solving
Project or business process management experience
Practical experience within active pharmaceutical ingredient (API) manufacturing
Knowledge or awareness of Good Manufacturing Practice and regulatory requirements
You do not need to meet every desirable criterion to apply. If your experience is relevant and you are motivated to develop your knowledge, we encourage you to consider the opportunity.
Why join us?
You’ll work across technical, operational and engineering teams, helping to improve how activities are planned and delivered. Your work will support safe and GMP compliant manufacturing within a dynamic pilot plant environment, supplying AZ’s exciting pipeline of medicines in development.
If you enjoy taking ownership, working through complex challenges and turning data into practical improvements to deliver products which change patients’ lives, we’d like to hear from you.
About AstraZeneca
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