Stability Coordinator

Intertek; Cambridgeshire and Peterborough; On-site; GBP 32,000 - 42,000; Full time

Benefits offered by this job

Permanent position

Training and progression

Collaborative team culture

Job summary

Intertek in Melbourn, Cambridgeshire, is recruiting a Stability Coordinator to support pharmaceutical stability studies in a GMP laboratory. You will coordinate sample storage, records and equipment to ensure compliance and timeliness.

The role requires a quality-focused, organised individual with good communication and IT skills. Training and progression opportunities exist within our global network.

Qualifications

• 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

Responsibilities

• Coordinate 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

Skills

Quality mindset

Organisational skills

Written & verbal comms

MS Office proficiency

GMP/regulatory experience

Stability operations experience

Scientific discipline qualification

Education

Scientific discipline qualification or relevant industry experience

Job description

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 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.

• Competitive salary and benefits package
• Permanent position within a growing cGMP laboratory environment
• Clear training, development and progression opportunities
• Supportive and collaborative team culture
• Opportunity 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