Quality Operations Manager

Talentmark; Burton upon Trent; On-site; GBP 60,000 - 75,000; Full time

Benefits offered by this job

Private Healthcare cover.

Company Pension Scheme.

Life Assurance.

Gym Discount.

Access to Wellness platforms.

Yearly Pay Reviews

Job summary

Talentmark is partnering with an established pharmaceutical manufacturer to appoint a Quality Operations Manager based at Burton upon Trent. You will lead a senior quality function within a highly regulated manufacturing site, ensuring sterile operations meet GMP, regulatory and patient safety standards.

The role reports to the Head of Quality and focuses on driving quality excellence, investigations, CAPAs, change control and risk management while mentoring colleagues and collaborating with

Qualifications

• Experienced quality leader with strong GMP knowledge.
• Experience in regulated pharmaceutical manufacturing environments.
• Proven project leadership and people-management experience.

Responsibilities

• Lead quality and sterility assurance activities across the site.
• Ensure GMP and regulatory compliance across operations.
• Manage investigations, CAPAs, change control and risk assessments.
• Drive continuous improvement of quality systems and processes.
• Develop and mentor colleagues and work with senior stakeholders.

Skills

Leadership

Quality Management

Risk Management

Education

Degree in Pharmacy or relevant science

Job description

Quality Operations Manager

Burton upon Trent | Site-Based

12 Month Fixed Term Contract (scope to be made permanent)

Talentmark is partnering with an 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 you'll 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, you'll 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.

Your Background:

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:

• Private Healthcare cover.
• Company Pension Scheme.
• Life Assurance.
• Gym Discount.
• Access to Wellness platforms.
• Yearly Pay Reviews