Senior Quality Assurance Officer
CK Group
- Cambridge
- Permanent
- Full-time
- Monitor and ensure compliance with relevant regulatory frameworks (GMP, GDP).
- Develop and maintain quality management system documentation including policies and procedures.
- Provide support to the QA Manager to ensure that any quality record is assigned to a QA representative, and that stages are completed in a timely manner.
- Manage and supervise a team of quality assurance professionals.
- Participate in risk assessments and develop strategist for risk mitigation.
- Identify areas for improvement and implement effective quality control measures.
- Ensure effective communication with all stakeholders.
- Ensuring all our suppliers meet our Company's high standards for quality and compliance.
- Leading and participating in QMS initiatives.
- BSc or MSc in a life science subject or comparable experience.
- Significant experience of working in quality assurance within the pharmaceutical or biotechnology industry, in a GMP compliant environment.
- Experience of performing external and internal audits.
- Strong communication skills, attention to detail and the ability to work collaboratively with cross functional teams.
- Comprehensive knowledge of regulations and quality standards relating to ATMPs.
New Scientist