Location: Midrand
Lead quality systems and compliance in a dynamic pharmaceutical environment!
Are you an experienced Quality Systems Manager with a strong background in pharmaceutical compliance?
This role offers the opportunity to oversee quality management systems, ensure regulatory adherence, and drive continuous improvement in a leading organization.
Key Responsibilities:
Develop, implement, and maintain the Pharmaceutical Quality Management System.
Ensure compliance with regulatory requirements, ISO standards, and global best practices.
Oversee quality systems, documentation, supplier management, and audits.
Align quality strategies across departments and branches.
Manage risk assessments, CAPA processes, change control, and regulatory deviations.
Lead and support internal and external audits, ensuring effective resolutions.
Who You Are:
Qualifications: Tertiary degree in science or quality management. Additional training in Total Quality Management is advantageous.
Experience: 4–5 years in Quality Management, including compliance, complaint handling, and manufacturing oversight (sterile manufacturing preferred).
Skills: Strong knowledge of cGMP principles, regulatory compliance, risk management, and strategic planning.
Competencies: Detail-oriented, deadline-driven, and skilled in problem-solving and leadership.
Technical Expertise: Proficiency in document control systems, digital tools, and regulatory reporting.
Take the lead in shaping quality strategies and ensuring excellence in pharmaceutical operations.
Apply today and be part of a high-impact team driving compliance and innovation!
Call Christine 084 627 3603 / christine@cbpro.co.za