Quality Assurance Professional
We are seeking an experienced quality assurance professional to support compliance with regulations. This permanent job offers the opportunity to work in a fast-paced, dynamic environment with strong scope for impact.
Key Responsibilities:
* Plan, schedule, and conduct internal and external audits to ensure compliance with standards.
* Review documentation and processes to guarantee adherence to regulatory requirements.
* Assess quality systems, including document control, deviations, and CAPA management to identify areas for improvement.
* Identify non-compliance issues, recommend corrective actions, and ensure timely follow-up to maintain regulatory compliance.
* Prepare clear audit reports and liaise with stakeholders on CAPA plans to facilitate collaborative problem-solving.
* Contribute to continuous improvement of quality processes by staying updated on regulatory changes and best practices.
Qualifying Criteria:
* Bachelor's degree in a science-related discipline such as chemistry or biology.
* 5+ years' experience in quality assurance or compliance in the pharmaceutical industry.
* Proven auditing experience in GMP/GDP environments with a strong understanding of regulatory requirements.
* Strong knowledge of regulations including GxP guidelines.
* Solid understanding of manufacturing processes, validation, and distribution.
* Excellent communication, organisational, and report-writing skills to effectively collaborate with cross-functional teams.
Additional Skills & Values:
* A detail-oriented professional with the ability to lead teams and drive results.
* Strong problem-solving skills and the ability to manage multiple priorities autonomously to meet deadlines.
* A collaborative team player who can drive engagement across the business to achieve common goals.
This role offers a unique opportunity to work in a fast-paced environment and contribute to the company's success by maintaining regulatory compliance and improving quality processes.