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- Tasks: Manage and improve utility systems and equipment in a biopharma facility.
- Company: Join a dynamic biopharmaceutical company focused on advanced therapies.
- Benefits: Enjoy a fast-paced environment with opportunities for innovation and growth.
- Why this job: Make a real impact in a cutting-edge industry while ensuring compliance and reliability.
- Qualifications: Degree in engineering or trades certification; 5-7 years in regulated biopharma settings.
- Other info: Collaborate with cross-functional teams to enhance operational efficiency.
The predicted salary is between 36000 - 60000 £ per year.
Facilities & Maintenance Engineer – Cleanroom & Biopharma
This is an exciting opportunity to join a fast-paced biopharmaceutical facility supporting the manufacture of advanced therapies. You’ll play a key role in the coordination and continuous improvement of utility systems and manufacturing equipment on-site, ensuring operational reliability and GMP compliance across all facilities.
What You\’ll Be Doing:
- Plan, execute, and supervise facility, process, and maintenance engineering in a highly regulated environment
- Oversee contractor activity for preventive maintenance and calibration, ensuring adherence to safety and permitting standards
- Support utility and facility installation and commissioning in capital projects
- Develop and carry out planned and reactive maintenance procedures
- Maintain compliance with GMP, HSE, and quality standards throughout the facility
- Support and maintain PPM schedules and contribute to internal improvement strategies
- Monitor equipment and building utility performance to ensure reliability for manufacturing operations
- Work cross-functionally to streamline processes and remove operational barriers
- Identify innovative and cost-effective engineering solutions to optimise operations
- Assist with budget planning and maintain critical spares inventory
- Ensure timely training and closeout of GMP documentation including deviations, CAPAs, change controls, and audit findings
Key Skills & Experience:
- Degree or technical qualification in an engineering discipline or trades certification
- 5–7 years minimum in a regulated industry with at least 3 years in a biopharma cleanroom facility
- Hands-on knowledge of HVAC systems, compressed air, oxygen, and other utility systems
- Background in facilities or maintenance engineering with exposure to GMP environments
- Familiarity with calibration planning is desirable
- Strong organisational and communication skills, with a proactive approach to problem-solving and innovation
What Success Looks Like:
- Improved utility and equipment reliability
- Contamination-free, GMP-compliant facility operations
- Asset care strategy development and measurable cost efficiency gains
- Strong working relationships across engineering and operations teams
If you\’re ready to bring your engineering expertise to a high-impact role in a forward-thinking biotech environment, apply today!
Facilities & Maintenance Engineer – Cleanroom & Biopharma employer: S3 Science Recruitment
Contact Detail:
S3 Science Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Facilities & Maintenance Engineer – Cleanroom & Biopharma
✨Tip Number 1
Familiarise yourself with the specific regulations and standards in the biopharma industry, especially GMP compliance. This knowledge will not only help you during interviews but also demonstrate your commitment to maintaining high operational standards.
✨Tip Number 2
Network with professionals in the biopharma sector, particularly those who work in cleanroom environments. Attend industry events or join relevant online forums to gain insights and potentially get referrals that could boost your application.
✨Tip Number 3
Prepare to discuss specific examples of how you've improved utility systems or equipment reliability in past roles. Highlighting your hands-on experience with HVAC systems and maintenance engineering will set you apart from other candidates.
✨Tip Number 4
Showcase your problem-solving skills by thinking of innovative solutions to common challenges faced in biopharma facilities. Being able to articulate these ideas during your interview can demonstrate your proactive approach and fit for the role.
We think you need these skills to ace Facilities & Maintenance Engineer – Cleanroom & Biopharma
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in facilities and maintenance engineering, particularly in biopharma cleanroom environments. Emphasise your hands-on knowledge of HVAC systems and any specific projects you've worked on that align with the job description.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Discuss how your background in regulated industries and your proactive problem-solving skills make you a perfect fit for the position. Be sure to mention any specific achievements related to GMP compliance and operational reliability.
Highlight Key Skills: When detailing your experience, focus on key skills mentioned in the job description, such as your ability to oversee contractor activities, support utility installations, and maintain compliance with HSE and quality standards. Use specific examples to demonstrate these skills in action.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial in a highly regulated environment like biopharma.
How to prepare for a job interview at S3 Science Recruitment
✨Showcase Your Technical Knowledge
Be prepared to discuss your hands-on experience with HVAC systems and other utility systems relevant to the biopharma cleanroom environment. Highlight specific projects where you ensured compliance with GMP standards.
✨Demonstrate Problem-Solving Skills
Prepare examples of how you've identified and implemented innovative engineering solutions in previous roles. This will show your proactive approach to overcoming operational barriers.
✨Emphasise Team Collaboration
Since the role involves working cross-functionally, be ready to share experiences where you successfully collaborated with different teams. This will illustrate your ability to build strong working relationships.
✨Understand Regulatory Compliance
Familiarise yourself with GMP, HSE, and quality standards relevant to the biopharma industry. Being able to discuss how you maintain compliance in your work will demonstrate your suitability for the role.
