QC Supervisor: Chemistry

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

If you do not receive a response from us within three weeks of submitting your application, please understand that your application was not successful.

Disclaimer:

Dear Applicant, we appreciate your interest in joining our organization. It is imperative for us that you understand how we handle your information. We are committed to ensuring the security and confidentiality of the information you provide. Your personal details will be collected for the sole purpose of the application process and will be used strictly for that purpose. By applying, you acknowledge and consent to the collection, use, and protection of your personal information in accordance with our privacy policy. If you have any inquiries or concerns, our Human Capital department is available to provide clarification. We look forward to reviewing your application.