QC Supervisor: Chemistry at Biovac

• BIOVAC is one of the leading sterile vaccine manufacturers rooted in Africa, with our core purpose being to "protect life". We are looking to hire a dynamic, passionate, confident, proactive and QC Supervisor: Chemistry to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Diploma or degree in Analytical Chemistry, Chemistry or equivalent.
• Recognition is given to Prior Learning and practical experience.

NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

• 3+ years experience in a pharmaceutical QC laboratory or equivalent of which at least one year should be at Senior Analyst level.
• 1 years Supervisory experience in pharmaceutical quality control or similar position would be an advantage.
• Quality and regulatory compliance knowledge, i.e. SAHPRA and WHO would be an advantage.
• Experience in having faced successful local and international quality audits would be an advantage.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• To ensure that the chemistry testing related activities are performed at the required quality levels (TBI, SAHPRA and WHO), within the agreed / budgeted time frame.
• Ensure undisrupted, punctual and safe operation of staff and processes pertaining to raw material release, finished products, intermediates, utilities and stability testing.
• Continually strive to deliver solutions through teamwork that ensures continuous improvement through innovative solutions.
• Active guidance and coaching of staff within section.
• Participating in project teams and supporting other relevant organisational departments.
• Ensuring compliance in accordance with the Medicines and Related Substances Act 101 of 1965, Pharmacy Act 53 of 1974 and the organizations policies, procedures and other applicable laws.
• Participation in quality audits and support to validation teams.
• Effective implementation of quality systems.
• Raw Material, intermediates, utility, stability and finished product testing.
• Ensuring that all EHS related issues are in order and responsible for Safety Reps.
• Ensure Change controls, Deviations, CAPAs and Risk Assessments are closed on time.
• Investigate all OOS/OOT generated in the Chemistry section.

Data Integrity Compliance:

• Ensure all laboratory data is recorded, reviewed, and stored in accordance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available).
• Promote a culture of data integrity by training staff on proper documentation practices and electronic data handling.
• Monitor and audit data management systems to detect and prevent data manipulation, omissions, or unauthorized access.
• Support implementation of secure, validated systems for electronic records and signatures in compliance with 21 CFR Part 11 and other applicable regulations

Application Deadline: 20 August 2025