Quality Control Inspector at Biovac

Qualifications Needed:

• Matric/ Grade 12 or equivalent.

Necessary Experience & Industry Knowledge:

• At least 1 years’ experience within the pharmaceutical/ vaccine manufacturing/ quality control or similar position.
• Experience in quality management systems within a cGMP facility.

Key Duties & Responsibilities:

• General warehouse/ logistics activities and support.
• Knowledge about equipment items and relevant procedures.
• Inspecting, sampling, testing, and documenting of incoming material.
• Retention sampling and status labelling.
• Maintaining electronic registers with regards to item release and rejection.
• Adhere to QC Quality systems and ensure high level of GLP and cGMP.
• Participate in projects, departmental audits and implement corrective actions where relevant.
• Compile or amend SOP’s where required.
• Contribute technical knowledge experience and learning to quality team with respect to assigned equipment/ processes.
• Proactive cost and expense management with risk identification and mitigation in own role.
• Ensure high level of GLP and GMP in assigned areas, equipment, and processes.
• Maintain up to date working knowledge of assigned equipment / processes – including knowledge of relevant guidelines.
• Ensure timely and effective communication.
• Sampling and testing of products, reagents, printed packaging material and production devices.
• Maintaining laboratory operations at cGMP, GLP standards to ensure quality, safety and regulatory compliance.
• Continually strive to deliver solutions through teamwork that ensures continuous improvement through innovation solutions.
• Achieving/ maintaining of the facilities and processes in full compliance with the current regulations and guidelines – both local and international.
• Participation in quality audits and support to project teams.