QA Associate

Quality Assurance (QA) Associate

Location: Remote

Position Overview:

This site is a centre of excellence for particle size reduction and integrated analytical services, supporting the pharmaceutical industry from early development through to commercial production. We handle highly potent and cytotoxic compounds and play a crucial role in ensuring the highest standards of product quality and patient safety.

We’re seeking a Quality Assurance (QA) Associate to join our team on a contract basis to help maintain world-class compliance across all manufacturing and analytical operations.

Responsibilities:

• Provide continuous QA support to the Operations team to ensure full compliance with both internal and regulatory quality standards.

• Conduct thorough batch record reviews, including overseeing SOW assessments and evaluating manufacturing and quality control (QC) data.

• Take charge of or assist with investigations into customer complaints and Corrective and Preventive Actions (CAPAs).

• Ensure all operations comply with EU, US, and global regulatory requirements.

• Collaborate with cross-functional teams to drive continuous improvement and uphold the integrity of the product.

What We’re Looking For:

• Experience in GMP environments with a solid understanding of regulatory compliance.

• A degree in a scientific discipline or relevant technical experience.

• Familiarity with Quality Management Systems (QMS) and Active Pharmaceutical Ingredient (API) manufacturing processes.

• Strong organisational skills and the ability to meet deadlines in a fast-paced environment.

• Excellent communication and teamwork abilities.

• Proficiency in Microsoft Office and digital systems.

• Prior experience with QA batch reviews would be beneficial.
  
  For more information please contact Rory Donnellan
  rdonnellan@barringtonjames.com