Senior Bioprocess Engineer — Scale-Up for Biologics

Placements24; The Islands (MS); On-site; USD 52,000 - 77,000; Full time

Benefits offered by this job

Relocation assistance

Competitive salary

Retirement savings plan

Growth opportunities

Job summary

Placements24 is seeking an experienced Senior Bioprocess Engineer to join the advanced manufacturing and development team in Paarl. You will design, optimize, and scale-up biopharmaceutical processes, including fermentation and cell culture, to deliver robust yields in a regulated environment.

Lead projects, drive CAPA activities, develop validation protocols, and mentor junior engineers. You will collaborate with R&D, QA, and manufacturing operations to ensure cGMP compliance and successful

Qualifications

• MSc or PhD in Biochemical Engineering, Chemical Engineering, or related field.
• Minimum of 6 years in biopharmaceutical process development and manufacturing.
• Strong understanding of cell culture/fermentation, bioreactor operation, and downstream processing.
• Experience with process scale-up, validation, and cGMP compliance.

Responsibilities

• Design, develop, and optimize upstream bioprocesses (fermentation, cell culture) for biologics production.
• Lead scale-up activities from laboratory to pilot and commercial manufacturing scales.
• Troubleshoot process deviations and implement CAPAs.
• Develop and execute process validation protocols and documentation.
• Collaborate with cross-functional teams including research, quality assurance, and manufacturing operations.
• Ensure compliance with cGMP regulations and other relevant industry standards in Paarl.
• Mentor junior engineers and contribute to technical development of the bioprocess engineering group.

Skills

Project leadership

Bioprocess know-how

Regulatory compliance

Education

MSc/PhD in Biochemical Engineering

Job description

Placements24 is seeking an experienced Senior Bioprocess Engineer to join the advanced manufacturing and development team in Paarl. You will design, optimize, and scale-up biopharmaceutical processes, including fermentation and cell culture, to deliver robust yields in a regulated environment.

Lead projects, drive CAPA activities, develop validation protocols, and mentor junior engineers. You will collaborate with R&D, QA, and manufacturing operations to ensure cGMP compliance and successful