Vaccine Process Scientist — DoE & cGMP

Biovac; Cape Town; On-site; ZAR 700,000 - 1,000,000; Full time

Job summary

Biovac is seeking a capable Scientist to drive S&I activities, including DoE design, analytical method development and method verification. You will lead design, planning and execution of experiments, interpret complex data, and ensure documentation and compliance within a biosafety level 3 setting.

The role emphasizes SME-level operation of analytical platforms, technology transfers, and rigorous adherence to cGMP and relevant pharmaceutical regulations, contributing to impactful vaccine

Qualifications

• Bachelor’s degree or diploma in Microbiology, Biochemistry, Chemistry or Process Engineering.
• MSc or equivalent industry experience.
• Experience with DoE protocols and analytical method development.
• Knowledge of cGMP and GLP guidelines.
• Ability to work under biosafety level 3 containment.

Responsibilities

• Design, plan and execute DoE protocols and related experiments.
• Perform laboratory experiments to support high-throughput and routine development.
• Execute analytical verification/qualification of existing methods and development of new methods.
• Prepare, analyze and interpret complex data sets; act as SME for relevant equipment.
• Assist with technology transfers from development to manufacturing, including clinical trial materials.
• Write and compile SOPs, WI and technical documentation.
• Ensure compliance with Medicines Act and Pharmacy Act, and internal policies.
• Support a strong quality culture aligned to cGMP.

Skills

DoE design

Analytical data interpretation

SOP/WI documentation

GxP knowledge

Team collaboration

Education

Bachelor’s degree or diploma in Microbiology/Biochemistry/Chemistry/Process Engineering or equivalent

MSc or equivalent industry experience

Job description

Biovac is seeking a capable Scientist to drive S&I activities, including DoE design, analytical method development and method verification. You will lead design, planning and execution of experiments, interpret complex data, and ensure documentation and compliance within a biosafety level 3 setting.

The role emphasizes SME-level operation of analytical platforms, technology transfers, and rigorous adherence to cGMP and relevant pharmaceutical regulations, contributing to impactful vaccine