Pharmaceutical Process Engineer
Pharmaceutical Process Engineer

Pharmaceutical Process Engineer

Northwich Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Develop and optimise pharmaceutical processes while ensuring compliance with industry standards.
  • Company: Join a leading firm in Life Sciences and Pharmaceutical manufacturing.
  • Benefits: Enjoy competitive contract rates and opportunities for career development.
  • Why this job: Work with cutting-edge technologies in a collaborative engineering team.
  • Qualifications: Bachelor's in Chemical Engineering and 5 years' experience in GMP environments required.
  • Other info: Experience with sterile processing and regulatory frameworks 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

Pharmaceutical Process Engineer employer: IO

As a leading employer in the pharmaceutical sector, we offer an exceptional opportunity for Process Engineers to engage with top-tier life sciences clients while working in a collaborative and innovative environment. Our commitment to employee growth is evident through our focus on career development, exposure to advanced technologies, and adherence to the highest regulatory standards, ensuring that you can thrive both professionally and personally. Join us to be part of a dynamic team that values sustainability and efficiency in process engineering.
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Contact Detail:

IO 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 the latest trends and technologies in process engineering.

Tip Number 2

Familiarise yourself with the specific regulatory frameworks such as cGMP, FDA, and EMA standards. Being well-versed in these regulations will not only enhance your knowledge but also demonstrate your commitment to compliance during interviews.

Tip Number 3

Prepare to discuss your experience with validation protocols like DQ, IQ, OQ, and PQ in detail. Be ready to provide examples of how you've successfully implemented these processes in past roles, showcasing your hands-on expertise.

Tip Number 4

Highlight any experience you have with multidisciplinary teams. Emphasise your communication and coordination skills, as collaboration is key in delivering integrated design solutions in this role.

We think you need these skills to ace Pharmaceutical Process Engineer

Pharmaceutical Process Development
PFD and P&ID Design
Equipment Selection
cGMP Compliance
FDA and EMA Regulatory Knowledge
Validation Protocols (DQ, IQ, OQ, PQ)
Process Scale-Up
Technology Transfer
Analytical Skills
Problem-Solving Skills
Technical Writing
Documentation Skills
Communication Skills
Coordination within Multidisciplinary Teams
Energy-Efficient Process Improvements
Commissioning and Qualification Activities
FAT/SAT Experience
Knowledge of Sterile/Aseptic Processing
Understanding of Biological Containment Principles
Familiarity with Key Process Equipment

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 familiarity with GMP standards, FDA/EMA regulations.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the pharmaceutical industry and your specific achievements in process engineering. Mention any experience with commissioning and qualification activities, as well as your ability to work within multidisciplinary teams.

Highlight Technical Skills: In your application, emphasise your technical writing abilities and experience with validation protocols (DQ, IQ, OQ, PQ). Provide examples of how you've implemented process improvements or supported technology transfers in previous roles.

Showcase Problem-Solving Abilities: Include specific instances where you've identified inefficiencies and successfully implemented solutions. This will demonstrate your analytical skills and your proactive approach to process engineering challenges.

How to prepare for a job interview at IO

Showcase Your Technical Expertise

Be prepared to discuss your experience with PFDs, P&IDs, and validation protocols. Highlight specific projects where you successfully implemented these skills, as this will demonstrate your capability to handle the technical demands of the role.

Understand Regulatory Standards

Familiarise yourself with cGMP, FDA, and EMA standards before the interview. Be ready to discuss how you've ensured compliance in past roles, as this knowledge is crucial for the position.

Demonstrate Problem-Solving Skills

Prepare examples of how you've identified inefficiencies and implemented process improvements in previous roles. This will show your analytical abilities and your proactive approach to engineering challenges.

Communicate Effectively

Since collaboration is key in this role, practice articulating your thoughts clearly and concisely. Be ready to discuss how you've worked within multidisciplinary teams and how you liaised with stakeholders to gather requirements.

Pharmaceutical Process Engineer
IO
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  • Pharmaceutical Process Engineer

    Northwich
    Full-Time
    36000 - 60000 £ / year (est.)

    Application deadline: 2027-08-27

  • I

    IO

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