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- Tasks: Develop and optimise pharmaceutical processes from design to technology transfer.
- 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 36000 - 60000 £ per year.
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iO Associates – UK/EU provided pay range
This range is provided by iO Associates – UK/EU. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
Direct message the job poster from iO Associates – UK/EU
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
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.
Seniority level
-
Seniority level
Mid-Senior level
Employment type
-
Employment type
Contract
Job function
-
Job function
Manufacturing
-
Industries
Pharmaceutical Manufacturing
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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 employers. This can help you gain insights into the latest trends and job openings.
✨Tip Number 2
Familiarise yourself with the specific technologies and processes mentioned in the job description, such as PFDs, P&IDs, and validation protocols. Being able to discuss these topics confidently during interviews will demonstrate your expertise and enthusiasm for the role.
✨Tip Number 3
Consider reaching out to current employees at iO Associates or similar companies on platforms like LinkedIn. Ask them about their experiences and any tips they might have for standing out in the application process.
✨Tip Number 4
Stay updated on regulatory changes and advancements in pharmaceutical manufacturing. Showing that you are proactive about your professional development can set you apart from other candidates and highlight your commitment to the field.
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 from your past roles to demonstrate your expertise.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention how your background aligns with the key responsibilities outlined in the job description, such as your experience with commissioning and qualification activities.
Highlight Technical Skills: Clearly outline your technical skills related to the position, such as your familiarity with validation protocols (DQ, IQ, OQ, PQ) and any hands-on experience with FAT/SAT. This will show that you have the practical knowledge needed for the role.
Showcase Problem-Solving Abilities: Include examples of how you've identified inefficiencies and implemented improvements in previous roles. This is crucial for demonstrating your analytical and problem-solving skills, which are essential for a Process Engineer.
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 validation protocols like DQ, IQ, OQ, and PQ. Highlight specific projects where you successfully implemented these processes, as this will demonstrate your hands-on knowledge and suitability for the role.
✨Understand Regulatory Standards
Familiarise yourself with cGMP, FDA, and EMA standards before the interview. Be ready to explain how you've ensured compliance in past roles, as this is crucial for a Pharmaceutical Process Engineer.
✨Emphasise Collaboration Skills
Since the role involves working within multidisciplinary teams, share examples of how you've effectively collaborated with others. Discuss any challenges faced and how you overcame them to deliver integrated design solutions.
✨Prepare for Problem-Solving Questions
Expect questions that assess your analytical and problem-solving skills. Think of specific instances where you identified inefficiencies and implemented improvements, and be ready to discuss the outcomes of those actions.
