Stability Coordinator

Intertek Group Plc; Melbourn; On-site; GBP 25,000 - 35,000; Full time

Benefits offered by this job

Development and career opportunities around the Globe

Working in a highly motivated team

Job summary

A leading global quality services company is seeking a motivated Stability Coordinator to join their team in Melbourn, UK. The role focuses on coordinating pharmaceutical stability studies while ensuring compliance with GMP and quality standards. Required skills include an attention to detail, proficiency in Microsoft Office, and a background in scientific disciplines. This position offers genuine development opportunities along with the chance to work in a dynamic environment committed to quality and safety.

Qualifications

• Ability to work accurately in accordance with established procedures.
• Experience within a GMP or regulated pharmaceutical environment is desirable.
• Experience of controlled climate rooms or pharmaceutical stability operations is beneficial.

Responsibilities

• Coordinate and support pharmaceutical stability activities ensuring compliance.
• Day-to-day operation of stability storage areas and equipment.
• Maintain accurate records for all stability studies.

Skills

Strong quality mindset with attention to detail

Good organizational skills

Clear written and verbal communication skills

Proficiency in Microsoft Office applications

Education

Qualifications in a scientific discipline

Relevant industry experience or quality control

Job description

As a Stability Coordinator, Intertek is recruiting for a motivated, organised and quality-focused individual to join our expanding team in Melbourn. Due to continued investment and sustained growth at our cGMP laboratory, this is an excellent opportunity to develop your career within a highly regulated, quality-driven environment.

Primarily, the role 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.

We recognise and reward capability and contribution, offering genuine development and progression opportunities based on performance.

Required skills and experience:

• Strong quality mindset with the ability to work accurately in accordance with established procedures
• Good organisational skills with strong attention to detail
• Clear written and verbal communication skills
• Proficiency in Microsoft Office applications
• Experience working within a GMP or regulated pharmaceutical environment (desirable)
• Experience of controlled climate rooms, cabinets or pharmaceutical stability operations (beneficial)
• Qualifications in a scientific discipline and/or quality control, or relevant industry experience

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 stability storage areas and specialist stability equipment
• Perform routine and ad-hoc sample storage, retrieval and removal activities
• Maintain accurate hard-copy and electronic records for all stability studies
• Organise and dispatch samples to internal and external customers
• Support preventative maintenance activities and equipment qualification
• Plan and organise workload effectively to meet agreed timelines
• Communicate clearly within the stability and wider laboratory teams
• Demonstrate a proactive, detail-focused and solution-oriented approach
• 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.

• Development and career opportunities around the Globe
• Working in a highly motivated team and dynamic working environment

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.