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Full-Time Opportunity: This is a permanent, full-time position with a competitive package and real career growth potential.
Job Description
- Support end-to-end manufacturing processes for biologics production (drug substance)
- Monitor and optimize process performance to ensure efficiency, quality, and compliance
- Troubleshoot process deviations and implement corrective and preventive actions (CAPA)
- Collaborate with cross-functional teams including Production, Quality, Validation, and Engineering
- Contribute to process validation activities and continuous improvement initiatives
- Ensure adherence to GMP, safety, and regulatory requirements
- Support documentation including SOPs, batch records, and technical reports
Your profile - Bachelor’s degree in Chemical Engineering, Biotechnology, Bioprocess Engineering, or related field
- 2–5+ years of experience in biopharmaceutical or biologics manufacturing
- Strong understanding of GMP and regulatory standards
- Experience in drug substance processes such as fermentation, purificat...