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- Tasks: Oversee critical process evaluations in API manufacturing and ensure compliance with production requirements.
- Company: Join a leading global pharmaceutical company at the forefront of manufacturing advancements.
- Benefits: Enjoy a long-term opportunity with state-of-the-art technology and a focus on production efficiency.
- Why this job: Be a key player in a major expansion project that impacts global health standards.
- Qualifications: Degree in Chemical or Process Engineering; experience in API manufacturing and CQV principles required.
- Other info: Hands-on experience with instrumentation systems is essential for this role.
The predicted salary is between 36000 - 60000 £ per year.
ENG Bauen is supporting a leading global pharmaceutical company in delivering a major expansion project, requiring an experienced Process Engineer to oversee critical process evaluations within an API manufacturing environment. This is an opportunity to play a key role in a high-value investment program, ensuring that Commissioning, Qualification, and Validation (CQV) activities align with production requirements.
Our client is making significant investments in state-of-the-art manufacturing technology to enhance production efficiency and maintain world-class pharmaceutical standards. As part of this strategic expansion, they require a Process Engineer to act as a key interface between CQV teams, Quality Assurance, and production operations, ensuring all process changes comply with regulatory and operational standards. This is an excellent long-term opportunity within a company at the forefront of pharmaceutical manufacturing advancements.
Key Responsibilities:- Act as the voice of production in evaluating CQV activities, ensuring new systems and modifications meet operational needs.
- Pre-approve qualification documents, verifying compliance before final QA sign-off.
- Assess and verify instrumentation changes, including valves, temperature sensors, and process control systems.
- Update P&IDs to reflect modifications within the production area.
- Ensure that all process changes align with GMP, safety, and regulatory standards.
- Degree in Chemical Engineering, Process Engineering, or related discipline.
- Strong experience in API manufacturing and process engineering within the pharmaceutical sector.
- Working knowledge of CQV principles, with experience in assessing qualification work from a production perspective.
- Familiarity with GMP, regulatory compliance, and quality assurance processes.
- Hands-on experience with valves, temperature sensors, and instrumentation systems.
- Ability to interpret and update P&IDs in response to system modifications.
If you are interested in this opportunity, please apply or send your CV via the ENG Bauen website or LinkedIn page.
Process Engineer employer: ENG Bauen Ltd
Contact Detail:
ENG Bauen Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Process Engineer
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those involved in API manufacturing. Attend industry conferences or local meetups to connect with potential colleagues and learn about the latest trends and technologies.
✨Tip Number 2
Familiarise yourself with the specific CQV processes used in the company you're applying to. Research their recent projects and any innovations they have implemented to demonstrate your knowledge during interviews.
✨Tip Number 3
Prepare to discuss your hands-on experience with instrumentation systems, as this is crucial for the role. Be ready to provide examples of how you've successfully managed process changes in compliance with GMP and regulatory standards.
✨Tip Number 4
Showcase your ability to work collaboratively with cross-functional teams. Highlight any past experiences where you acted as a liaison between production and quality assurance, as this will be key in the role you're applying for.
We think you need these skills to ace Process Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in API manufacturing and process engineering. Emphasise your familiarity with CQV principles and any hands-on experience with instrumentation systems.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the key responsibilities mentioned in the job description. Explain how your background aligns with the requirements, particularly your experience in evaluating CQV activities and ensuring compliance with GMP standards.
Highlight Relevant Skills: In your application, clearly outline your skills related to regulatory compliance, quality assurance processes, and your ability to interpret and update P&IDs. Use specific examples from your past work to demonstrate these skills.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.
How to prepare for a job interview at ENG Bauen Ltd
✨Know Your Technical Stuff
Make sure you brush up on your knowledge of API manufacturing processes and CQV principles. Be prepared to discuss specific examples from your past experience that demonstrate your expertise in these areas.
✨Understand Regulatory Standards
Familiarise yourself with GMP and other regulatory compliance standards relevant to the pharmaceutical industry. Being able to articulate how you've ensured compliance in previous roles will impress your interviewers.
✨Showcase Your Problem-Solving Skills
Be ready to discuss challenges you've faced in process engineering and how you overcame them. Highlight your ability to assess and verify instrumentation changes, as well as your experience with P&IDs.
✨Communicate Effectively
As a Process Engineer, you'll need to act as a liaison between various teams. Practice articulating your thoughts clearly and concisely, especially when discussing complex technical concepts.
