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Quality Operations Manager
Job Location:
Job Location:
Burton upon Trent - UK
Yearly Salary:
£ £ 50000 - 60000
Yearly Salary:
Posted:
7 October 2026 (6 hours ago)
Posted:
Application Deadline:
4 January 2027
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Quality Operations Manager
Burton upon Trent Site-Based
12 Month Fixed Term Contract (scope to be made permanent)
Talentmark is partnering withan established pharmaceutical manufacturer seeking an experienced Quality Operations Manager to join its senior quality leadership team.
This is a key role within a highly regulated manufacturing environment where youll be responsible for leading quality and sterility assurance activities and ensuring the highest standards of GMP compliance and patient safety.
The Role:
Reporting to the Head of Quality youll lead a skilled quality function and play a key role in driving quality excellence across the manufacturing operation.
Responsibilities:
An experienced Quality leader with a strong background in a regulated pharmaceutical manufacturing environment.
Essential:
Benefits:
The organisation offers a competitive salary and comprehensive benefits package including:
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 71439 in all correspondence.
Burton upon Trent Site-Based
12 Month Fixed Term Contract (scope to be made permanent)
Talentmark is partnering withan established pharmaceutical manufacturer seeking an experienced Quality Operations Manager to join its senior quality leadership team.
This is a key role within a highly regulated manufacturing environment where youll be responsible for leading quality and sterility assurance activities and ensuring the highest standards of GMP compliance and patient safety.
The Role:
Reporting to the Head of Quality youll lead a skilled quality function and play a key role in driving quality excellence across the manufacturing operation.
Responsibilities:
- Lead quality and sterility assurance activities across the site.
- Ensure compliance with GMP and regulatory requirements.
- Managing investigations CAPAs change control and quality risk management.
- Driving continuous improvement across quality systems and processes.
- Developing and mentoring colleagues.
- Working closely with senior stakeholders regulators and wider quality teams.
An experienced Quality leader with a strong background in a regulated pharmaceutical manufacturing environment.
Essential:
- Degree in Pharmacy or a relevant science discipline
- Project management experience within aseptic processing compounding or sterile manufacturing.
- Strong knowledge of GMP regulatory requirements and quality systems.
- Proven project leadership and people-management experience.
- Experience managing investigations CAPAs change control and risk management.
- Experience of process improvement projects or change implementation.
Benefits:
The organisation offers a competitive salary and comprehensive benefits package including:
- Private Healthcare cover.
- Company Pension Scheme.
- Life Assurance.
- Gym Discount.
- Access to Wellness platforms.
- Yearly Pay Reviews
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 71439 in all correspondence.
About Company
Idibu
100 employees
Every business is now operating in an environment that’s susceptible to change. idibu has evolved against this changing backdrop. Whether driven by legislation, technology, customer demand or the economy, businesses now need to be agile and fleet of foot to ensure they can attr ... View more
