Looking for skilled scientists and engineers with 3 to 8 years of hands-on experience in peptide process development to join our dynamic, innovation-driven CDMO team.
Open Roles & Responsibilities
- Process R&D (Peptide Synthesis)
Ideal for scientists with a strong foundation in solid and solution-phase peptide synthesis. - Execute complex Solid Phase Peptide Synthesis (SPPS) up to 30–40 mer peptides
- Work with diverse acid and amide resins (2-CTC, Rink Amide, Wang, MBHA, etc.)
- Perform cleavage, deprotection, and isolation with precision and safety
- Implement Fmoc/Boc strategies, cyclizations, and peptide modifications
- Operate automated synthesizers (Liberty Blue, CEM) and manual reactors (1–10L)
- Maintain robust documentation in eLN and contribute to GMP execution
Analytical R&D (Peptide Purification)
- For professionals experienced in purifying complex peptides and ensuring high product quality.
- Expertise in peptide purification using preparative RP-HPLC and other chromatographic techniques
- Perform method optimization to achieve desired purity, yield, and recovery
- Operate and troubleshoot HPLC systems, and manage scale-up purification processes
- Collaborate with PR&D and Process Engineering teams to ensure smooth downstream workflows
- Document purification strategies and contribute to analytical report generation and batch records
Process Engineering (Tech Transfer & Scale-Up)
- Focused on enabling smooth transitions from lab-scale synthesis to GMP manufacturing.
- Drive technology transfer of peptide processes into pilot/GMP facilities
- Design efficient, scalable, and compliant manufacturing processes
- Ensure plant readiness and cross-functional alignment across production phases
Send your resume to: krishnafulsure@aurigeneservices.com | pranavgayal@aurigeneservices.com