Remote Biologics Process Engineer

Placements24; East London; Hybrid; ZAR 1,667,000 - 2,668,000; Full time

Benefits offered by this job

Health insurance

Performance bonuses

Retirement planning

Fully remote role

Job summary

Placements24 is seeking a Biologics Process Engineer to design, optimize, and scale bioprocessing workflows for biologics production in a fully remote role. You will work on upstream and downstream technologies, drive process development from lab to manufacturing scales, and ensure GMP compliance.

The ideal candidate has 4+ years of hands‑on experience in biologics process development, strong modeling and data analysis skills, and the ability to work independently in a remote setting while

Qualifications

• Master's or PhD in Chemical Engineering, Biochemical Engineering, Biotechnology, or a related field.
• Minimum of 4 years of hands‑on experience in process development and scale‑up of biologics manufacturing.
• Strong understanding of upstream (cell culture, fermentation) and downstream (chromatography, filtration, purification) bioprocessing technologies.
• Experience with GMP manufacturing environments and regulatory requirements for biologics.
• Proficiency in process modeling software and data analysis tools.

Responsibilities

• Design, develop, and optimize bioprocessing workflows for the manufacture of biologics (e.g., monoclonal antibodies, recombinant proteins, vaccines).
• Scale‑up processes from laboratory bench to pilot and commercial manufacturing scales.
• Troubleshoot and resolve technical issues related to bioreactors, cell culture, purification systems, and other bioprocessing equipment.
• Develop and validate process models and parameters to ensure consistent product quality and yield.
• Collaborate with R&D scientists, manufacturing teams, and quality assurance personnel to ensure seamless process transfer and implementation.
• Author and review process development reports, technical protocols, and standard operating procedures (SOPs).
• Ensure all processes adhere to Good Manufacturing Practice (GMP) regulations and industry best practices.
• Conduct process hazard analyses and implement necessary safety measures.
• Stay current with emerging technologies and methodologies in bioprocessing and biologics manufacturing.

Skills

Bioprocess engineering

Cell culture

Fermentation

Scale-up

GMP

Process modeling

Data analysis

Documentation

Education

Master's or PhD in Chemical Engineering / Biochemical Engineering / Biotechnology

Job description

About the Role

Our client, a pioneering biotechnology firm focused on developing innovative biologic therapies, is seeking a talented Biologics Process Engineer to join their advanced engineering team on a fully remote basis. This role is crucial for designing, optimizing, and scaling up bioprocessing operations for the manufacture of complex biological molecules. You will leverage your expertise in upstream and downstream processing, cell culture, fermentation, and purification techniques to enhance efficiency, yield, and quality. This remote position provides an outstanding opportunity to work on cutting-edge projects within the biopharmaceutical industry, contributing to the advancement of life‑saving treatments from the convenience of your own workspace, anywhere in the world.

Key Responsibilities

• Design, develop, and optimize bioprocessing workflows for the manufacture of biologics (e.g., monoclonal antibodies, recombinant proteins, vaccines).
• Scale‑up processes from laboratory bench to pilot and commercial manufacturing scales.
• Troubleshoot and resolve technical issues related to bioreactors, cell culture, purification systems, and other bioprocessing equipment.
• Develop and validate process models and parameters to ensure consistent product quality and yield.
• Collaborate with R&D scientists, manufacturing teams, and quality assurance personnel to ensure seamless process transfer and implementation.
• Author and review process development reports, technical protocols, and standard operating procedures (SOPs).
• Ensure all processes adhere to Good Manufacturing Practice (GMP) regulations and industry best practices.
• Conduct process hazard analyses and implement necessary safety measures.
• Stay current with emerging technologies and methodologies in bioprocessing and biologics manufacturing.

Requirements

• Master's or PhD degree in Chemical Engineering, Biochemical Engineering, Biotechnology, or a related field.
• Minimum of 4 years of hands‑on experience in process development and scale‑up of biologics manufacturing.
• Strong understanding of upstream (cell culture, fermentation) and downstream (chromatography, filtration, purification) bioprocessing technologies.
• Experience with GMP manufacturing environments and regulatory requirements for biologics.
• Proficiency in process modeling software and data analysis tools.
• Excellent problem‑solving skills and a systematic approach to process optimization.
• Strong written and verbal communication skills, with the ability to document technical information clearly.
• Ability to work independently, manage multiple projects, and meet project timelines in a remote setting.
• Experience with single‑use technologies and continuous manufacturing is a plus.

Benefits

• Our client offers a competitive salary and a comprehensive benefits package, including health insurance, performance bonuses, and retirement planning.
• This is a fully remote role, offering exceptional flexibility and the ability to work from anywhere.
• You will have access to cutting‑edge technology and opportunities for continuous learning and professional development.
• Join a dynamic and innovative team at the forefront of biotechnology, contributing to the development of life‑changing therapies.
• We value collaboration, innovation, and the well‑being of our remote workforce.