QA Coordinator – Pharma Compliance & Documentation

Cencora, Inc.; South Normanton; On-site; GBP 26,000 - 31,000; Full time

Job summary

Cencora, Inc. is recruiting for a Quality Assurance role at our South Normanton operation. You will contribute to safe handling of healthcare products, maintain quality records and support product release activities.

The role offers 40 hours per week, Monday to Friday, in a regulated environment where GDP, GMP and ISO 9001 standards drive daily activities. Attention to detail and a proactive mindset are essential for success.

Qualifications

• Strong attention to detail and a conscientious approach to your work.
• Good organisation and prioritisation skills, with the ability to manage different tasks and deadlines.
• Clear and confident communication skills.
• A proactive and flexible approach, with a willingness to learn and take on new responsibilities.
• Confidence working with documentation, records and administrative processes.
• Previous experience within Quality Assurance or regulated environments would be beneficial, but isn’t essential.

Responsibilities

• Support day-to-day quality and compliance activities across the site.
• Review temperature records and monitoring data, helping ensure products are stored and handled correctly.
• Record, investigate and elevate complaints and quality incidents in line with established processes.
• Support administrative product release activities.
• Maintain accurate QA documentation, SOPs and quality records.
• Support the team with audits, inspections and corrective actions.
• Work with colleagues across the operation to help maintain high quality and compliance standards.
• Provide general administrative support to the wider QA team.

Skills

Attention to detail

Organisation

Communication

Willingness to Learn

Documentation

QA Knowledge

Job description

Cencora, Inc. is recruiting for a Quality Assurance role at our South Normanton operation. You will contribute to safe handling of healthcare products, maintain quality records and support product release activities.

The role offers 40 hours per week, Monday to Friday, in a regulated environment where GDP, GMP and ISO 9001 standards drive daily activities. Attention to detail and a proactive mindset are essential for success.