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Associate Director, Chemical Development

Job in Macclesfield, Cheshire, SK11, England, UK
Listing for: AstraZeneca
Part Time position
Listed on 2026-02-13
Job specializations:
  • Pharmaceutical
    Drug Discovery, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 80000 - 100000 GBP Yearly GBP 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Associate Director Chemical Developer

Location:

Macclesfield Competitive salary and Benefits Hybrid working 3 days a week in the office About us

At AstraZeneca, we're united by a bold ambition: to push the boundaries of science and deliver life‑changing medicines to patients worldwide. As a global, science‑led biopharmaceutical company, we transform pioneering research into breakthrough treatments across oncology, cardiovascular, respiratory, and rare diseases. Here, your talent will contribute to innovations that truly matter—helping us reimagine healthcare and create a healthier future for all!

Introduction

to role

Are you ready to lead world‑class small molecule chemistry development that turns bold science into reliable medicines for patients? In this role, you will set the technical direction for your team and elevate how we design, scale, and validate robust drug substance processes—reducing risk, shortening timelines, and enabling confident clinical supply and launch!

Small molecule Active Pharmaceutical Ingredients (APIs) remain a powerful modality for tackling disease. The complexity of small molecule therapeutics continues to grow, necessitating innovative and efficient means for their synthesis and manufacture to meet volume, cost and sustainability goals.

We are seeking a highly skilled and motivated leader to join the Chemistry function in AstraZeneca’s Chemical Development department as Associate Director – Chemistry.

You will be responsible for leading a team within the Chemistry function developing synthetic manufacturing processes and supporting regulatory documentation. Working closely with the Senior Director for Chemistry to deliver aspects of the Small Molecule development strategy and drive successful delivery of the projects portfolio through Phase 3‑enabling clinical development to commercialisation. Do you thrive when you can mentor scientists, deliver strategic goals, and see tangible impact on medicines reaching patients faster?

Accountabilities

Lead a team of Synthetic Chemists to deliver the Chemistry contribution to small molecule drug substance projects, with responsibility for:

  • Synthetic process development with associated scale‑up assessment, and control strategy development
  • Technology transfer and support of clinical drug substance manufacture and process validation
  • Delivery of CMC regulatory submissions for clinical and marketing – acting as reviewer
  • Driving effective collaboration with other skill groups to deliver drug substance projects

Line management of Synthetic Chemists, including:

  • Coaching and mentoring to support professional development, including onboarding of new starters
  • Performance management – goal setting and regular feed‑forward to drive impactful contributions
  • Driving SHE and compliance for team
Contribute to the Chemistry development strategy
  • Lead improvement projects to enhance the capability and capacity of the Chemistry function to deliver their contribution to drug substance projects
  • Drive uptake of improved standards and ways of working within the Chemistry function
Essential Skills/Experience
  • Degree or equivalent experience in Chemistry + demonstrated experience in synthetic drug substance process development
  • Evidence of people leadership skills through previous responsibilities, including coaching and mentoring of scientists
  • Track record of leading development and scale‑up of synthetic chemistry to deliver commercially viable manufacturing processes, including understanding of the contribution of analytical chemistry, chemical engineering, and particle science
  • Good understanding of the drug development process, especially late‑stage development to support Phase 3 clinical studies and launch including control strategy development
  • Proven experience in authoring module 3.2 regulatory submissions
Desirable Skills/Experience
  • Previous people management experience, including performance management and individual development
  • Experience of reviewing module 3.2 regulatory submissions
  • Evidence of driving the introduction of digital approaches and new synthetic manufacturing technology
  • Good project management skills and the ability to drive multiple projects…
Position Requirements
10+ Years work experience
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