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Pilot Plant Project Coordinator

AstraZeneca
Macclesfield, GBR
Full-time
Mid
Onsite
Discovered 4 days ago

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.

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