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For Companies At a Glance
- Tasks: Develop and optimise pharmaceutical processes from design to commissioning.
- Company: Join a leading firm in Life Sciences and Pharmaceutical manufacturing.
- Benefits: Enjoy competitive contract rates and career development opportunities.
- Why this job: Work with cutting-edge technologies in a collaborative engineering team.
- Qualifications: Bachelor's in Chemical Engineering and 5 years in GMP-regulated environments required.
- Other info: Experience with sterile processing and regulatory compliance is preferred.
The predicted salary is between 42000 - 84000 £ per year.
Job Description
About the Role
We are seeking an experienced Process Engineer to work in close partnership with the Director of Process Technology, delivering projects for leading Life Sciences and Pharmaceutical manufacturing clients. This role will involve end-to-end process engineering support, from early design through to commissioning, qualification, and technology transfer.
Key Responsibilities
-
Develop pharmaceutical processes, including PFDs, P&IDs, and equipment selection.
-
Collaborate within multidisciplinary project teams to deliver integrated design solutions.
-
Ensure compliance with cGMP, FDA, and EMA standards; support QRA and HAZOP activities.
-
Support process scale-up and technology transfer between development and manufacturing.
-
Identify inefficiencies and implement throughput and process improvements.
-
Oversee Commissioning & Qualification activities: DQ, IQ, OQ, PQ; support FAT/SAT.
-
Liaise with stakeholders to gather requirements and present technical solutions.
-
Recommend sustainable, energy-efficient process improvements.
-
Produce high-quality technical reports, documentation, and compliance records.
Qualifications & Experience
✅ Bachelor's Degree in Chemical Engineering (or related discipline).
✅ Minimum 5 years' experience in a GMP-regulated pharmaceutical/life sciences environment.
✅ Strong understanding of GMP standards, FDA/EMA regulatory frameworks.
✅ Proven experience with validation protocols (DQ, IQ, OQ, PQ).
✅ Ability to design PFDs, P&IDs and participate in equipment selection.
✅ Experience with process scale-up and technology transfer.
✅ Strong analytical and problem-solving skills.
✅ Excellent technical writing and documentation skills.
✅ Strong communication and coordination skills within multidisciplinary teams.
Preferred Skills
⭐ Experience with sterile/aseptic processing, biopharmaceutical manufacturing, or high-containment facilities.
⭐ Knowledge of ATEX compliance, solvent handling, and powder handling in pharmaceutical settings.
⭐ Understanding of biological containment principles.
⭐ Familiarity with key process equipment (reactors, fermenters, filtration units, CIP/SIP systems, cleanroom utilities).
⭐ Hands-on experience with FAT/SAT, commissioning, and equipment qualification.
Why Join?
-
Opportunity to work with leading pharmaceutical and life sciences manufacturers.
-
Gain exposure to cutting-edge process technologies and regulatory compliance frameworks.
-
Join a collaborative, technically strong engineering team with significant career development potential.
-
Competitive contract rates.
Desired Skills and Experience
Pharmaceutical Process Engineer (Contract)
About the Role
We are seeking an experienced Process Engineer to work in close partnership with the Director of Process Technology, delivering projects for leading Life Sciences and Pharmaceutical manufacturing clients. This role will involve end-to-end process engineering support, from early design through to commissioning, qualification, and technology transfer.
Key Responsibilities
Develop pharmaceutical processes, including PFDs, P&IDs, and equipment selection.
Collaborate within multidisciplinary project teams to deliver integrated design solutions.
Ensure compliance with cGMP, FDA, and EMA standards; support QRA and HAZOP activities.
Support process scale-up and technology transfer between development and manufacturing.
Identify inefficiencies and implement throughput and process improvements.
Oversee Commissioning & Qualification activities: DQ, IQ, OQ, PQ; support FAT/SAT.
Liaise with stakeholders to gather requirements and present technical solutions.
Recommend sustainable, energy-efficient process improvements.
Produce high-quality technical reports, documentation, and compliance records.
Qualifications & Experience
✅ Bachelor's Degree in Chemical Engineering (or related discipline).
✅ Minimum 5 years' experience in a GMP-regulated pharmaceutical/life sciences environment.
✅ Strong understanding of GMP standards, FDA/EMA regulatory frameworks.
✅ Proven experience with validation protocols (DQ, IQ, OQ, PQ).
✅ Ability to design PFDs, P&IDs and participate in equipment selection.
✅ Experience with process scale-up and technology transfer.
✅ Strong analytical and problem-solving skills.
✅ Excellent technical writing and documentation skills.
✅ Strong communication and coordination skills within multidisciplinary teams.
Preferred Skills
⭐ Experience with sterile/aseptic processing, biopharmaceutical manufacturing, or high-containment facilities.
⭐ Knowledge of ATEX compliance, solvent handling, and powder handling in pharmaceutical settings.
⭐ Understanding of biological containment principles.
⭐ Familiarity with key process equipment (reactors, fermenters, filtration units, CIP/SIP systems, cleanroom utilities).
⭐ Hands-on experience with FAT/SAT, commissioning, and equipment qualification.
Why Join?
Opportunity to work with leading pharmaceutical and life sciences manufacturers.
Gain exposure to cutting-edge process technologies and regulatory compliance frameworks.
Join a collaborative, technically strong engineering team with significant career development potential.
Competitive contract rates.
Pharmaceutical Process Engineer employer: iO Associates - UK/EU
Contact Detail:
iO Associates - UK/EU Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmaceutical Process Engineer
✨Tip Number 1
Network with professionals in the pharmaceutical and life sciences sectors. Attend industry conferences, webinars, or local meetups to connect with potential colleagues and learn about job openings that may not be advertised.
✨Tip Number 2
Familiarise yourself with the latest trends and technologies in pharmaceutical process engineering. Being knowledgeable about cutting-edge processes can help you stand out during interviews and discussions with hiring managers.
✨Tip Number 3
Prepare for technical interviews by reviewing common questions related to GMP standards, validation protocols, and process design. Practising your responses will help you articulate your experience and expertise more confidently.
✨Tip Number 4
Showcase your problem-solving skills by preparing examples of past projects where you identified inefficiencies and implemented improvements. This will demonstrate your ability to contribute effectively to multidisciplinary teams.
We think you need these skills to ace Pharmaceutical Process Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in pharmaceutical process engineering. Focus on your skills in developing PFDs, P&IDs, and your understanding of GMP standards. Use specific examples to demonstrate your expertise.
Craft a Strong Cover Letter: Write a cover letter that addresses the key responsibilities outlined in the job description. Explain how your background aligns with their needs, particularly your experience with commissioning and qualification activities.
Highlight Technical Skills: In your application, emphasise your technical writing and documentation skills. Mention any experience you have with validation protocols and process scale-up, as these are crucial for the role.
Showcase Team Collaboration: Since the role involves working within multidisciplinary teams, include examples of past collaborations. Highlight your communication skills and how you've successfully liaised with stakeholders to deliver projects.
How to prepare for a job interview at iO Associates - UK/EU
✨Showcase Your Technical Expertise
Be prepared to discuss your experience with PFDs, P&IDs, and equipment selection. Highlight specific projects where you successfully developed pharmaceutical processes, as this will demonstrate your technical capabilities.
✨Understand Regulatory Standards
Familiarise yourself with cGMP, FDA, and EMA standards. Be ready to explain how you've ensured compliance in previous roles, as this is crucial for the position.
✨Demonstrate Problem-Solving Skills
Prepare examples of how you've identified inefficiencies and implemented process improvements. This will show your analytical skills and ability to enhance productivity.
✨Communicate Effectively
Since collaboration is key in this role, practice articulating your thoughts clearly. Be ready to discuss how you've liaised with multidisciplinary teams and stakeholders to deliver integrated design solutions.
