About the Role
Our client, a leading biopharmaceutical company dedicated to advancing novel therapeutics, is seeking a talented Biopharmaceutical Process Development Scientist to join their innovative team in Soweto, Gauteng . This role focuses on the development, optimization, and scale-up of manufacturing processes for biologics, including monoclonal antibodies and recombinant proteins. The ideal candidate will possess a strong understanding of cell culture, upstream processing, downstream purification, and process characterization techniques. You will be instrumental in ensuring the efficient and robust production of high-quality biopharmaceuticals, contributing significantly to bringing life-changing treatments to patients. This is an exciting opportunity for a scientist passionate about bioprocess engineering to grow their career within a rapidly evolving sector in Soweto .
Key Responsibilities
- Lead and execute process development activities for upstream (cell culture) and downstream (purification) operations of biologics.
- Optimize existing biomanufacturing processes to improve yield, purity, and reduce costs.
- Develop and validate robust analytical methods for in-process controls and product characterization.
- Design and conduct experiments using Design of Experiments (DoE) principles for process understanding and optimization.
- Troubleshoot and resolve technical challenges encountered during process development and scale-up activities.
- Prepare comprehensive process development reports, technology transfer documents, and contributions to regulatory filings.
- Collaborate with upstream and downstream manufacturing teams to ensure successful technology transfer and implementation of processes.
- Stay current with the latest advancements in bioprocessing technologies and methodologies.
- Ensure all activities are conducted in compliance with cGMP, safety, and environmental regulations.
- Contribute to building a strong scientific and technical culture within the biopharmaceutical development group in Gauteng .
Requirements
- Ph.D. or Master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, or a related field.
- Minimum of 4 years of hands‑on experience in biopharmaceutical process development, including upstream and downstream processing.
- Demonstrated experience with cell culture/fermentation and/or protein purification techniques.
- Proficiency with process characterization, scale‑up, and technology transfer principles.
- Experience with process analytical technology (PAT) and DoE is highly desirable.
- Strong analytical and problem‑solving skills, with the ability to interpret complex data.
- Excellent written and verbal communication skills, with experience in technical report writing.
- Ability to work independently and as part of a cross‑functional team.
- Knowledge of regulatory requirements for biopharmaceuticals (e.g., FDA, EMA) is a plus.
- Commitment to scientific excellence and innovation in the Soweto region.
Benefits
- Annual salary of R.
- Comprehensive health, dental, and vision insurance coverage.
- Performance‑based bonus and annual reviews.
- Generous paid time off and company holidays.
- Opportunities for professional development, including attending conferences and workshops.
- Retirement savings plan with employer matching.
- Access to state‑of‑the‑art bioprocessing equipment and facilities.
- A dynamic and collaborative work environment focused on innovation in Gauteng .
- Career advancement prospects within a leading biopharmaceutical company.