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QC Lead: Chemistry & Material Handling

Job in Cape Town, 7100, South Africa
Listing for: Biovac
Full Time position
Listed on 2026-01-22
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Control / Manager, QA Specialist / Manager, Quality Technician/ Inspector
Job Description & How to Apply Below

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 meticulous QC Lead:
Chemistry & Material Handling to join a goal-oriented team.

QUALIFICATIONS NEEDED:
  • Degree or diploma in Chemistry / Analytical Chemistry / Biochemistry or equivalent.
  • Recognition is given to Prior Learning and practical experience.
NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:
  • At least 6 years' experience in vaccine / pharmaceutical / biotech manufacturing industry.
  • At least 3 years' experience at management level.
  • Experience in quality and regulatory compliance within a cGMP facility.
  • Strong leadership and team management abilities.
  • Experience with LIMS, chromatography data systems and /or electronic documentation systems.
  • Proficient in method and data review.
  • Proven troubleshooting and problem‑solving abilities within analytical testing.
KEY DUTIES & RESPONSIBILITIES OF

THE ROLE:
  • Drive continuous improvement plans and priorities through the implementations of appropriate tools or methodologies to proactively manage risk, reduce wastage and to improve quality on site.
  • Management of all Materials (Raw Material and Packaging) testing and Chemistry testing activities for product release.
  • Participation in project teams as QC representative.
  • Assist with the transfer of analytical methods from technology transfer partners to Biovac and their implementation in the laboratory.
  • Assist with compiling of analytical method validation / verification protocols and reports.
  • Assist with selection of analytical test equipment and participation in equipment qualification e.g., review of qualification documents.
  • Assist with writing and updating of material and product specifications and test methods and standard operating procedures.
  • Liaison with suppliers on technical issues where applicable.
  • Maintaining laboratory operations at cGMP standards to ensure quality, safety and regulatory compliance.
  • Departmental Management of the QC laboratory budget, ensuring alignment with GMP and regulatory requirements.
  • Forecast costs for analytical testing, stability studies, reference standards, and consumables.
  • Control expenditure related to equipment calibration, maintenance, and outsourced testing.
  • Collaborate with procurement to optimize vendor contracts for reagents, instruments, and lab services.
  • Prepare CAPEX proposals for new analytical technologies and lab upgrades.
  • Monitor budget performance, analyze variances, and implement corrective actions.
  • Maintaining that Stability Program, including compiling stability protocols and reports.
  • Ensure that relevant testing is performed according to the Biovac Stability Program.
  • Assist with the compilation of stability protocols and reports.
  • Participation in quality audits and closing any gaps of findings.
  • Ensure that OOS and OOT investigations are initiated and completed to the correct standard.
  • Identify and / or participate in inspections, investigations, risk management and quality review exercises.
  • Chemistry testing to support aseptic vaccine manufacturing performed to required quality and regulatory standards and within agreed time frames.
  • Chemistry assay qualifications, validations, and verifications.
  • Undisrupted, punctual, and safe operation of staff and processes pertaining to Chemistry Testing and the institutes operations.
  • Technology transfer activities involving Chemistry testing within the agreed time frames.
  • Review specifications, test methods and other QC procedures.
  • Ensure the qualification and maintenance of premises and equipment used by the Chemistry team.
  • Ensure that the required initial and continuing training of his teams personnel is carried out and adapted according to need.
  • Responsible to ensure that the Material Handling (Raw Material and Packaging Materials) sections deliver services and solutions in alignment with pharmaceutical quality system requirements.
  • Approve or reject starting materials, packaging materials intermediate bulk and finished product.
  • Co‑ordinate sampling and testing of sampling materials, packaging materials, components production devices, intermediate, bulk and…
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