Join a team improving lives through innovative science
About us
GlycoSyn is a leader in complex synthetic chemistry and GMP manufacturing, specialising in the contract development and GMP manufacture of pharmaceutical actives and ingredients to support the commercialisation of new, life‑changing medicines.
Established in 2003 and with a track record of over 20 years of successful operation as part of a public sector agency, GlycoSyn has recently been acquired and is taking its first steps as a new entity, GlycoSyn Technologies Ltd. This is a unique opportunity to join the team during a period of dynamic change and projected growth.
If you enjoy hands‑on problem‑solving, thrive in a technical environment, and want to grow within a highly regulated and innovative industry—this could be your next step.
For more information visit us at www.glycosyn.com
About the Role
We are seeking a motivated and hands-on Facilities Engineer to support the operation, maintenance, and continuous improvement of equipment, utilities, and infrastructure within a GMP manufacturing environment.
This is a dynamic, cross-functional role where you’ll not only ensure facilities and systems operate safely and reliably but also contribute directly to manufacturing operations. Working alongside experienced professionals, you’ll gain exposure across engineering, maintenance, and pharmaceutical production, making this an excellent opportunity for someone looking to broaden their technical capability in a highly regulated industry.
We welcome applicants from a range of backgrounds including pharmaceutical, biotechnology, chemical processing, advanced manufacturing, or laboratory environments transitioning into operations.
About You
You are a proactive, detail-oriented engineer who enjoys solving complex problems in a regulated environment. You bring strong technical capability, sound judgement, and the ability to balance independent work with team collaboration.
What You’ll Do
Facilities & Equipment Management
Ensuring reliable performance of utilities and equipment (HVAC, purified water, compressed air, environmental monitoring, process equipment).
Performing and overseeing preventative and corrective maintenance.
Leading troubleshooting and root‑cause investigations.
Maintaining asset, maintenance, and calibration records to GMP standards.
Supporting equipment lifecycle activities—including URS, FAT/SAT, commissioning, qualification, and decommissioning.
Compliance & Quality
Ensuring facilities operate in alignment with GMP, FDA, EMA, and PIC/S guidelines.
Supporting internal and external audits.
Maintaining SOPs, engineering documents, and validation protocols.
Participating in deviations, CAPAs, and change control processes.
Project Engineering
Managing upgrade projects from scoping through to execution and qualification.
Coordinating contractors, vendors, and internal stakeholders.
Identifying opportunities for facility optimisation and energy efficiency.
Operational Support
Providing engineering support to ensure uninterrupted manufacturing operations.
Responding to alarms, deviations, and urgent maintenance needs.
Assisting with environmental monitoring and cleanroom readiness.
Cross‑training to support operator duties where required.
Health, Safety & Environment
Ensuring all activities meet EHS requirements and safe‑work procedures.
Participating in hazard identification, incident reporting, and safety improvement initiatives.
Promoting a strong safety culture across the facility.
What You’ll Bring
Required
Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical, Mechatronics, or similar) or equivalent technical qualification.
Experience in GMP, pharmaceutical, biotech, medical device or other highly regulated manufacturing environments.
Strong understanding of utilities and facility systems (HVAC, purified water, compressed air, environmental controls).
Knowledge of maintenance systems, calibration processes, and equipment qualification.
Ability to interpret engineering drawings, P&IDs, and technical documentation.
Excellent problem‑solving skills and sound technical judgement.
Preferred
Experience with Computer Maintenance Management Systems.
Experience in commissioning and qualification (IQ/OQ/PQ).
Knowledge of Lean, Six Sigma, or reliability methodologies.
Experience working cross‑functionally in fast‑paced manufacturing environments.
Understanding of regulatory frameworks such as FDA 21 CFR 210/211, EU GMP, and PIC/S.
Why Join Us?
Work with cutting‑edge technology in a purpose‑driven organisation.
Contribute directly to the delivery of life‑changing products.
Be part of a supportive, highly skilled team in a collaborative environment.
Grow your skills across engineering, maintenance, and pharmaceutical operations.
How to Apply
If you’re ready to grow your career in a highly regulated manufacturing environment and want to make a genuine impact, we’d love to hear from you.
Apply now with your CV and a brief cover letter outlining your experience