Bioprocess Engineer

Placements24; Klerksdorp; On-site; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Competitive salary

Growth opportunities

State-of-the-art facilities

Collaborative team

PTO & retirement plan

Job summary

Placements24 is seeking a Bioprocess Engineer to join its R&D team in Klerksdorp, SA. You will develop and optimize biologics manufacturing processes, including scale-up and technology transfer, while ensuring GMP-compliant operations and robust product quality.

The role requires 3–5 years of biopharma experience, hands-on bioreactor and cell culture expertise, and strong problem-solving skills within a collaborative environment.

Qualifications

• Bachelor's or Master's degree in Chemical Engineering, Biochemical Engineering, or related field.
• 3–5 years of biopharmaceutical process development or manufacturing experience.
• Hands-on experience with bioreactor operation, cell culture, fermentation, and downstream processing.
• Knowledge of GMP and regulatory requirements for biopharmaceutical manufacturing.
• Strong analytical and problem-solving skills with attention to detail.
• Excellent teamwork and ability to communicate complex information clearly.

Responsibilities

• Design, develop, and optimize microbial or mammalian cell culture processes for biologics production.
• Perform process validation, scale-up studies, and technology transfer.
• Monitor and control bioprocess parameters to ensure quality and yield.
• Troubleshoot deviations and implement corrective actions to maintain performance.
• Collaborate with R&D, QA, and manufacturing teams.
• Prepare technical reports and presentations on process development activities.

Skills

Bioprocess development

GMP knowledge

Analytical skills

Team collaboration

Education

Chemical/Biochemical Engineering

Job description

About the Role

Our client is seeking a skilled Bioprocess Engineer to join their cutting-edge research and development team located in Klerksdorp . This role focuses on the development, optimization, and scale-up of biopharmaceutical manufacturing processes. You will be instrumental in ensuring the efficient and effective production of biologic drugs, working with advanced bioreactor systems and downstream processing equipment. This is an excellent opportunity to contribute to life-changing therapies and grow your career in a collaborative and scientifically driven organization that values innovation and operational excellence.

Key Responsibilities

• Design, develop, and optimize microbial or mammalian cell culture processes for the production of biologics.
• Perform process validation, scale-up studies, and technology transfer activities.
• Monitor and control bioprocess parameters to ensure product quality and yield.
• Troubleshoot process deviations and implement corrective actions to maintain process performance.
• Collaborate with R&D scientists, quality assurance, and manufacturing teams.
• Prepare technical reports, documentation, and presentations on process development activities.

Requirements

• Bachelor's or Master's degree in Chemical Engineering, Biochemical Engineering, or a related field.
• 3-5 years of experience in biopharmaceutical process development or manufacturing.
• Hands-on experience with bioreactor operation, cell culture, fermentation, and downstream processing.
• Knowledge of regulatory requirements (e.g., GMP) relevant to biopharmaceutical manufacturing.
• Strong analytical and problem-solving skills with attention to detail.
• Ability to work effectively in a team environment and communicate technical information clearly.

Benefits

• Competitive salary and comprehensive benefits package.
• Opportunities for professional growth and development in a leading biotech company.
• State-of-the-art laboratory and manufacturing facilities.
• Collaborative team environment focused on innovation.
• Paid time off and retirement savings plan.