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Process Scientist

Job in Wrexham, Wrexham County, LL13, Wales, UK
Listing for: Ipsen Biopharm Ltd
Full Time position
Listed on 2026-06-01
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 GBP Yearly GBP 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Title

Process Scientist

Company

Ipsen Biopharm Ltd

About Ipsen

Ipsen is a mid‑sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas:
Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K., we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries.

We build a workplace that champions human‑centric leadership and fosters a culture of collaboration, excellence and impact.

Location

Wrexham

Job Description

Join Ipsen Wrexham at an exciting time, where you’ll contribute to the manufacture of novel and innovative oncology therapies. This is a unique opportunity to advance cutting‑edge treatments, working at the forefront of science to deliver life‑changing medicines for patients worldwide. We’re looking for a proactive and scientifically driven Process Scientist to join our Manufacturing Science & Technology (MS&T) team. In this role, you’ll support process optimisation, continuous improvement, and technology transfer activities across drug product manufacturing.

You’ll play a key role in introducing new products. This is a temporary role until the end of Dec‑2027.

Key Responsibilities
  • Generate documentation including SOPs, protocols, reports, batch manufacturing instructions and training materials.
  • Lead and support process optimisation and continuous improvement projects to enhance manufacturing performance.
  • Design, execute, and document experimental protocols to generate high‑quality data.
  • Analyse and interpret data, delivering clear and accurate technical reports.
  • Support technology transfer and new product introduction into commercial manufacturing.
  • Collaborate cross‑functionally to deliver MS&T objectives and resolve process challenges.
Knowledge, skills and experience
  • Experience from a relevant department with an understanding of pharma manufacturing e.g. MS&T, Quality, Production, Engineering.
  • Experience with documentation in a GMP environment e.g. protocols, reports, SOPs and batch records.
  • Some lab/pilot plant knowledge to trial manufacturing processes when necessary.
  • Ability to deal with ambiguity and pivot at pace.
EEO Statement

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve.

This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.

Additional Information

Apply today and help drive innovation and excellence. #LI-Hybrid

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