Job Description
Key Responsibilities:
- Manage end-to-end peptide manufacturing operations (Solid Phase Peptide Synthesis – SPPS / Liquid Phase Synthesis)
- Ensure adherence to cGMP, USFDA, WHO, and other regulatory guidelines
- Handle scale-up and tech transfer from R&D to commercial production
- Monitor production planning, batch execution, and timely delivery
- Optimize processes to improve yield, quality, and cost efficiency
- Lead and develop a high-performing production team
- Ensure proper documentation (BMR, BPR, SOPs) and audit readiness
- Coordinate with QA, QC, R&D, and Engineering teams
- Drive continuous improvement initiatives and troubleshoot process issues
- Participate in regulatory audits and ensure compliance readiness
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