Quality Assurance Officer

Cure Talent; Sevenoaks; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading Pharmaceutical CDMO is seeking a QA Officer to ensure compliance with regulatory standards through Batch Review & Release. The role involves maintaining quality documentation, supporting audits, and collaborating with internal teams to uphold quality assurance practices.

Qualifications

• Proven experience in Quality Assurance within a pharmaceutical or GMP setting.
• Expertise in Batch Review & Release and understanding of GxP regulations.

Responsibilities

• Lead Batch Review & Release activities ensuring compliance with regulatory standards.
• Develop and maintain the Pharmaceutical Quality System (PQS).
• Conduct inspections and maintain documentation of quality assurance activities.

Skills

Quality Assurance

Problem Solving

Organisational Skills

Job description

Cure Talent is thrilled to partner with a leading Pharmaceutical CDMO who, due to their exceptional continued growth, have an exciting opportunity for a QA Officer to join their team, focusing on Batch Review & Release to ensure their products and processes meet strict regulatory standards.

In this role, you will take a lead inBatch Review & Release, ensuring compliance with regulatory guidelines. You will also be responsible for maintaining quality documentation, supporting audits, and working closely with the internal teams to uphold industry-leading quality assurance practices.

Key Responsibilities:

• Lead Batch Review & Release activities, ensuring all products comply with regulatory and industry standards
• Develop, implement, and maintain the Pharmaceutical Quality System (PQS)
• Conduct inspections, assessments, and reviews of products, processes, and equipment to ensure compliance
• Maintain accurate and comprehensive documentation of all quality assurance activities
• Support internal audits and assist in external audits conducted by regulatory bodies and clients

What You Will Need:

• Proven experience in Quality Assurance, ideally within a pharmaceutical or GMP setting
• Expertise in Batch Review & Release and understanding of GxP regulations
• Experience with quality management systems, deviation investigations, and CAPA management
• Strong organisational and problem-solving skills, with attention to detail
• Ability to work collaboratively within cross-functional teams and independently

If you are passionate about quality assurance and keen to work in a fast-paced, collaborative environment, we would love to hear from you!