Quality Assurance Specialist

About the Role

Our client is looking for a detail-oriented and process-driven Quality Assurance Specialist to join their operations team in Nottingham . This role is responsible for ensuring that the company's pharmaceutical products and processes comply with stringent quality standards and regulatory requirements. You will be involved in audits, inspections, documentation review, and continuous improvement initiatives. This hybrid position allows for remote work on certain tasks, complemented by necessary on-site activities for inspections and team collaboration.

Key Responsibilities

• Conduct internal audits and support external audits and regulatory inspections.
• Review and approve quality-related documentation, including SOPs, batch records, and validation reports.
• Investigate deviations, non-conformances, and CAPAs (Corrective and Preventive Actions).
• Monitor quality metrics and identify areas for process improvement.
• Ensure compliance with relevant regulations (e.g., GMP, GDP) and company quality policies.
• Participate in validation activities for equipment, processes, and computer systems.

Requirements

• Bachelor's degree in a scientific, technical, or related field.
• Minimum of 2 years of experience in a Quality Assurance or Quality Control role within the pharmaceutical industry.
• Strong understanding of GMP (Good Manufacturing Practice) and/or GDP (Good Distribution Practice) guidelines.
• Experience with quality management systems and documentation review.
• Excellent analytical, problem-solving, and communication skills.
• Ability to work independently and manage multiple tasks effectively.

Benefits

• Competitive annual salary and performance bonus.
• Comprehensive medical, dental, and vision insurance.
• Retirement savings plan with employer matching.
• Generous holiday allowance and sick leave.
• Opportunities for training and certification in quality management systems.