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- 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 significant 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 36000 - 60000 £ per year.
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.41bf1e1f-b16b-4260-a40a-17c77a06fd15
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 set you apart during interviews and discussions with hiring managers.
✨Tip Number 3
Prepare to discuss specific projects you've worked on that relate to the key responsibilities of the role. Highlight your experience with PFDs, P&IDs, and any successful process improvements you've implemented.
✨Tip Number 4
Showcase your understanding of regulatory compliance by being ready to discuss how you've ensured adherence to cGMP, FDA, and EMA standards in your previous roles. This will demonstrate your capability to handle the responsibilities of the position.
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. Emphasise your familiarity with GMP standards, FDA/EMA regulations, and any specific projects that showcase your skills in developing PFDs and P&IDs.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention specific projects or experiences that align with the job description, particularly your experience with commissioning and qualification activities.
Highlight Technical Skills: Clearly outline your technical skills related to process engineering, such as validation protocols (DQ, IQ, OQ, PQ) and your ability to produce high-quality technical reports. This will demonstrate your capability to meet the job requirements.
Showcase Problem-Solving Abilities: Provide examples of how you've identified inefficiencies and implemented improvements in past roles. This will illustrate your analytical skills and your proactive approach to process optimisation.
How to prepare for a job interview at iO Associates - UK/EU
✨Know Your Processes
Make sure you have a solid understanding of pharmaceutical processes, including how to develop PFDs and P&IDs. Be prepared to discuss your experience with equipment selection and how it relates to the role.
✨Familiarise Yourself with Regulations
Brush up on cGMP, FDA, and EMA standards. Being able to demonstrate your knowledge of these regulations during the interview will show that you are well-prepared and understand the importance of compliance in the pharmaceutical industry.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've identified inefficiencies in past roles and implemented process improvements. Highlighting your analytical skills and ability to work within multidisciplinary teams will be key.
✨Communicate Effectively
Strong communication is crucial in this role. Practice articulating your thoughts clearly and concisely, especially when discussing technical solutions or presenting reports. This will help you stand out as a candidate who can liaise effectively with stakeholders.
