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- Tasks: Develop and implement innovative processes for life-changing solutions in a collaborative R&D team.
- Company: Join a leading Life Sciences company making a real impact on human health.
- Benefits: Enjoy a competitive rate, modern facilities, and a supportive work environment.
- Why this job: Be part of a purpose-driven team where your contributions directly benefit patients worldwide.
- Qualifications: HNC or higher in Science/Engineering with experience in process engineering and validation.
- Other info: Opportunity to work with advanced tools and collaborate across various disciplines.
The predicted salary is between 48000 - 60000 £ per year.
Location: Stevenage
Duration: 12 months
Rate: up to £23.08/hour PAYE
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 will 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 will support the development, transfer, and implementation of processes and test methods - ensuring that high-quality, scalable solutions are ready for production.
Key Responsibilities:
- 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.
About You:
- HNC or higher in a Science or Engineering discipline.
- Strong background in process engineering and validation.
- Experienced in PFMEA, Lean methodologies, and quality systems.
- Excellent technical documentation and reporting skills.
- Strong collaboration skills with a proactive approach to problem-solving.
Desirable:
- Experience in analytical method validation and process transfer.
- Familiarity with CAD (SolidWorks), Minitab, and statistical analysis tools.
What's in it for you:
- Join a purpose-driven team developing solutions that positively impact human health.
- Work in a modern R&D facility with advanced tools and equipment.
- Collaborate across disciplines in an environment that fosters growth, learning, and innovation.
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.
Process Engineer in Stevenage employer: Manpower
Contact Detail:
Manpower Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Process Engineer in Stevenage
✨Tip Number 1
Familiarise yourself with the specific processes and technologies used in Fibro Membrane Chromatography. Understanding the nuances of this technology will not only help you during interviews but also demonstrate your genuine interest in the role.
✨Tip Number 2
Network with professionals in the Life Sciences industry, particularly those who work in process engineering. Attend relevant conferences or webinars to connect with potential colleagues and learn more about the latest trends and challenges in the field.
✨Tip Number 3
Brush up on your knowledge of Lean methodologies and quality systems, as these are crucial for the role. Consider taking a short online course or certification to enhance your skills and show your commitment to continuous improvement.
✨Tip Number 4
Prepare to discuss your experience with technical documentation and validation processes in detail. Be ready to provide examples of how you've successfully implemented these in past roles, as this will be key to demonstrating your fit for the position.
We think you need these skills to ace Process Engineer in Stevenage
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in process engineering, particularly in areas like validation and documentation. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the life sciences industry and your specific interest in the Process Engineer position. Mention any relevant projects or experiences that align with the responsibilities outlined in the job description.
Highlight Technical Skills: Emphasise your technical skills related to PFMEA, Lean methodologies, and statistical analysis tools like Minitab. Provide examples of how you've applied these skills in previous roles to solve problems or improve processes.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a role focused on quality and documentation.
How to prepare for a job interview at Manpower
✨Showcase Your Technical Skills
Make sure to highlight your experience with process engineering and validation during the interview. Be prepared to discuss specific projects where you implemented new processes or equipment, as well as your familiarity with tools like pFMEA and Lean methodologies.
✨Prepare for Collaboration Questions
Since the role involves working closely with R&D, Production, and Quality teams, expect questions about teamwork and collaboration. Think of examples where you successfully worked in a team to solve problems or improve processes.
✨Demonstrate Your Problem-Solving Approach
The company values a proactive approach to problem-solving. Be ready to share instances where you identified issues and took the initiative to resolve them, particularly in relation to process development or validation.
✨Know Your Documentation
As documentation is a key part of the role, brush up on your knowledge of SOPs, work instructions, and validation reports. Be prepared to discuss how you ensure accuracy and compliance in your technical documentation.
