
Research Scientist
2 days ago
Department: R&D – Process Development
Industry: CDMO / API
Purpose of the Role:
To lead and execute the development, optimization, and scale-up of robust, cost-effective, and regulatory-compliant chemical processes for Active Pharmaceutical Ingredients (APIs) and intermediates, ensuring smooth technology transfer from lab to kilo lab and manufacturing.
Key Responsibilities
1. Strategic Responsibilities
- Drive innovation by designing synthetic routes that align with project timelines and regulatory requirements.
- Contribute to technology differentiation strategies that enhance the CDMO's scientific credibility and client value proposition.
- Collaborate with cross-functional teams (Analytical, QA/QC, Regulatory) to support integrated drug development solutions.
2. Operational Responsibilities
- Perform route scouting, literature search, and develop robust and scalable chemical processes using QbD principles.
- Conduct laboratory experiments for reaction optimization, impurity profiling, and process safety assessment.
- Prepare and review technical reports, SOPs, and technology transfer documents.
- Ensure compliance with GMP/GLP and EHS standards during lab-scale and pilot-scale operations.
- Participate in troubleshooting during scale-up or commercial production batches and provide technical support during client audits.
3. Financial Responsibilities
- Optimize process economics by reducing cycle time, yield improvement, and minimizing raw material costs.
- Support cost estimation activities during project proposals or client RFQs by providing technical insights.
4. People & Collaboration Responsibilities
- Guide junior team members on experimental planning, data interpretation, and documentation best practices.
- Promote a culture of safety, learning, and innovation within the team.
- Work closely with Program Management and Business Development to align project goals with customer expectations.
Qualifications & Experience
- M.Sc ( Organic Chemistry)
- 3–9 years of experience in Process R&D, preferably in CDMO organizations
- Hands-on expertise in synthesis, scale-up, impurity profiling, and technology transfer
- Familiarity with analytical techniques (HPLC, GC, NMR) and regulatory documentation
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