Due to continued growth and increased programme demand within our Melbourn cGMP laboratories, Intertek is recruiting for a Stability Coordinator to support critical pharmaceutical stability activities. This role plays a vital part in ensuring samples are managed accurately, compliantly and on time within a highly regulated environment.
ABOUT YOU
As a Stability Coordinator, Intertek is recruiting for a motivated, organised and detail-focused individual to join our Stability team in Melbourn. This is a great opportunity for candidates without a scientific background who have an interest in working within a laboratory environment. We welcome applicants from administration, logistics, coordination, operations or similar structured environments who can demonstrate accuracy, responsibility and the ability to follow procedures.
You will work as an integral part of the Stability Team, supporting the coordination and execution of pharmaceutical stability studies while ensuring compliance with GMP, regulatory and quality standards. Intertek offers clear development and progression opportunities for individuals who demonstrate capability and commitment.
Required skills and experience:
* Highly organised with strong attention to detail and accuracy
* Ability to follow written protocols and procedures precisely (training provided)
* Methodical and reliable approach to routine, process-driven work
* Confidence completing paperwork and maintaining accurate records
* Clear written and verbal communication skills
* Ability to work independently and take responsibility for tasks
* Physically capable of manual handling and working across a two-floor facility with no lift
* Early morning availability to support stability pulls and a 12:30pm shipment deadline (flexibility available for strong candidates)
* Experience in a GMP, laboratory, logistics or regulated environment (desirable, not essential)
* Scientific qualifications or laboratory experience (nice to have, not essential)
ABOUT THE OPPORTUNITY
On a daily basis, you will coordinate and support pharmaceutical stability activities, ensuring samples, records and equipment are managed accurately and compliantly within a GMP laboratory environment.
Key activities:
* Coordination of pharmaceutical stability activities in compliance with current GMP and regulatory requirements
* Day-to-day operation of temperature- and humidity-controlled stability storage areas and equipment
* Routine and ad-hoc sample storage, retrieval, preparation and disposal activities
* Accurate completion, scanning and maintenance of hard-copy and electronic stability records
* Organisation and dispatch of samples to internal laboratories, external clients and external laboratories
* Support routine facility and equipment checks, including preventative maintenance activities
* Plan and organise workload effectively to meet daily timelines and shipment deadlines
* Communicate clearly within the stability team and wider laboratory groups
* Work priorities agreed with the Stability Team Leader, with increasing autonomy as experience develops
WHAT WE OFFER
Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues.We are a global family that values diversity and we thrive working together with precision, pace, and passion.We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.
* Competitive salary and benefits package
* Permanent position within a growing cGMP laboratory environment
* Clear training, development and progression opportunities
* Supportive and collaborative team cultureOpportunity to develop a long-term career within Intertek’s global network
We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.
Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies
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