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