QA Batch Release Officer

Capio Spine Center Stockholm; Runcorn; On-site; GBP 35,000 - 41,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking 3 Quality Assurance Batch Release Officers for its Runcorn location. The role involves overseeing product compliance, quality investigations, and documentation. Applicants should have a life science degree and relevant experience in quality assurance. The position offers a shift pattern and the opportunity to join a dynamic team focused on quality and compliance.

Qualifications

• Relevant experience in quality assurance or quality control preferred.
• Experience in the pharmaceutical or healthcare industry desired.
• Knowledge of GMP requirements for sterile manufacturing is a plus.

Responsibilities

• Review batch documentation to assess product compliance.
• Determine product disposition for market release or rejection.
• Support investigations of non-conformities affecting quality.

Skills

Quality Assurance

Compliance

Documentation

GMP knowledge

Education

Degree in a life science field

Tools

SAP

Job description

QA Batch Release Officer
Runcorn
Pharmaceutical industry
£35,000 inclusive of shift allowance plus Bonus
Permanent

Shift Pattern: 7:00 AM - 3:00 PM & 3:00 PM - 11:00 PM, Monday to Friday

About the Role

We are currently seeking an additional 3 Quality Assurance Batch Release Officers to join our client's QC Release team. These roles are key in ensuring product compliance and quality standards, working within cGMP and ISO guidelines. Reporting to the Shift Team Leader, you will oversee batch documentation, product disposition, and quality investigations to maintain high operational standards.

Due to the location and hours of work access to your own transport is essential.

The client is also happy to look at recent Graduates for these roles so please apply now to be considered!

Key Responsibilities

• Review batch documentation to assess product compliance.
• Determine product disposition for market release, internal use, or rejection.
• Support investigations of non-conformities affecting quality or compliance.
• Contribute to QA efficiency and on-time product release targets.
• Assist in continuous improvement initiatives within the quality system.
• Compile Certificates of Conformance as required.
• Maintain QA databases and support trend analysis.
• Collaborate with internal departments to uphold quality standards.
• Manage outsourced product transactions on SAP.

What We're Looking For

• Degree in a life science field or relevant experience in quality assurance / quality control.
• Experience in the pharmaceutical or healthcare industry preferred.
• Knowledge of GMP requirements for sterile manufacturing (clean room) is desirable or general experience of working within a GMP environment.
• Familiarity with sterile operations or compounding is a plus.

If you're passionate about quality and compliance and want to contribute to a dynamic team, we'd love to hear from you. Apply today!


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