Quality Assurance Officer

JR United Kingdom; Maidstone; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading Pharmaceutical CDMO in Maidstone is on the lookout for a QA Officer to enhance their operations. The role involves leading Batch Review & Release activities to meet regulatory standards and maintaining quality documentation. Ideal candidates will have proven Quality Assurance experience within the pharmaceutical sector and a passion for ensuring top-notch quality in a collaborative setting.

Qualifications

• Proven experience in Quality Assurance, ideally in pharmaceuticals.
• Expertise in Batch Review & Release processes and GxP regulations.
• Experience with quality management systems and CAPA management.

Responsibilities

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

Skills

Organisational skills

Problem-solving skills

Attention to detail

Collaboration

Education

Proven experience in Quality Assurance

Background in pharmaceutical or GMP setting

Job description

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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!