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Process Engineer

JR United Kingdom

Stevenage

On-site

GBP 40,000 - 70,000

Full time

Yesterday
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Job summary

An established industry player in the Life Sciences sector is seeking a Process Engineer to join their innovative R&D team in Stevenage. This role involves developing and implementing manufacturing processes that are crucial for producing life-changing solutions in vaccines and therapies. You will collaborate with R&D, Production, and Quality teams to ensure high-quality, scalable solutions are ready for production. If you have a strong background in Process Engineering and a keen eye for detail, this opportunity offers a chance to make a significant impact in a collaborative environment.

Qualifications

  • Strong Process Engineering background with validation expertise.
  • Experience in analytical method validation and process transfer.

Responsibilities

  • Develop and implement new manufacturing processes and equipment.
  • Create and maintain documentation including SOPs and validation reports.

Skills

Process Engineering
Validation Requirements
PFMEA
DMAIC
Lean
Statistical Analysis

Education

HNC in Science/Engineering

Tools

CAD (SolidWorks)
Minitab
Statistical Analysis Tools

Job description

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Our client, a leader in the Life Sciences industry, is looking for a Process Engineer to join their Fibro Membrane Chromatography R&D team at their state-of-the-art facility in Stevenage. You’ll be part of a collaborative and innovative environment, working to develop life-changing solutions used in vaccines, medicines, and cutting-edge therapies.

As a key link between R&D and Manufacturing, you'll support the development, transfer, and implementation of processes and test methods – ensuring that high-quality, scalable solutions are ready for production

What you’ll do:

  • Develop and implement new processes and equipment for manufacturing lines.
  • Create and maintain documentation including SOPs, work instructions, and validation reports.
  • Support Design for Manufacturability (DFM) initiatives using tools like pFMEA and Process Flow Charts.
  • Lead or support qualification activities (FAT, SAT, IQ, OQ, PQ).
  • Carry out method development, validation, and technical reports.
  • Provide statistical analysis of process capability (e.g., CpK/Ppk).
  • Collaborate closely with R&D, Production, and Quality teams.

Who you are:

  • Min HNC (Higher National Certificate) in Science/Engineering discipline.
  • Strong Process Engineering background and a detailed understanding of validation requirements for machine equipment, analytical methods and process.
  • Experienced in PFMEA, DMAIC, 5S, Lean.
  • Strong documentation skills (SOP, work instructions, IQ/OQ, URS, manufacturing plans, experimental reports, validation) with a keen eye for detail
  • Work independently on work packages and collaborate well with many functions within R&D and Production.

It would be a plus if you also possess previous experience in:

  • Experience in analytical method validation and process transfer.
  • Familiarity with CAD (SolidWorks), Minitab, and statistical analysis tools.

Apply now to be part of a team where your work truly matters – to your colleagues, the business, and most importantly, to patients around the world.

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