Associate Principal QA Specialist (CQV)

1. Provide shoulder-to-shoulder review, approval, and support for the management of quality records such as Deviations, CAPA, Change Controls, and Investigations to uphold GMP standards.
2. Oversee daily quality assurance activities within Validation and Technical Services areas, ensuring alignment with corporate requirements, standards, and regulatory guidelines including USFDA and European regulations.
3. Utilize GMP knowledge to manage and escalate major and critical compliance issues via the site’s QMS processes.
4. Actively identify, suggest, and contribute to continuous improvement initiatives to enhance quality systems and performance.
5. As the QA SME, support departmental Quality Councils and project meetings, offering technical guidance and strategic input.

• A Degree or higher level in a scientific discipline (e.g., Pharmaceutical Chemistry, Quality Assurance, Quality Management).
• Proven experience spanning 5–10 years in a QA role within a GMP biotech or pharmaceutical environment, demonstrating comprehensive knowledge of validation and GMP compliance.
• Familiarity with database management, risk-based decision making, and PQS processes, along with strong communication and interpersonal skills.
• Excellent problem-solving, organizational, and decision-making abilities, with a commitment to quality and continuous improvement.

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.