Pharmaceutical Specialist

4 weeks ago

Hyderabad, India Options Executive Search Private Limited Full time

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About the Company


The Catalyst Development & Scale-Up In charge will lead the research, development, optimization, and scale-up of catalyst systems used in pharmaceutical manufacturing processes. This role bridges laboratory innovation with plant-level implementation, ensuring efficient, cost-effective, and compliant production of high-quality intermediates and APIs. The position requires strong expertise in catalysis chemistry, process knowledge, scale-up methodologies and precious metal inventory management.


About the Role

The Catalyst Development & Scale-Up In charge will lead the research, development, optimization, and scale-up of catalyst systems used in pharmaceutical manufacturing processes.


Responsibilities


Catalyst Research & Development

  • Design, synthesize, and optimize heterogeneous and/or homogeneous catalysts for pharmaceutical reactions. Particularly, Pd, Pt, Ru, Rh on supports like activated carbon, alumina and other supports.
  • Very good fundamental understanding on catalysis, particularly pharma catalysts and good organic chemistry to understand the reaction mechanisms.
  • Conduct lab-scale experiments to evaluate catalyst activity, selectivity, stability, and recyclability.
  • Perform mechanistic studies to understand reaction pathways and catalyst behavior.
  • Screen novel catalytic systems for yield improvement, loss of precious metal, process efficiency, and sustainability.


Process Scale-Up

  • Translate lab-scale catalytic processes into pilot and commercial-scale operations.
  • Develop scale-up protocols considering heat/mass transfer, reactor design, and safety requirements.
  • Optimize reaction conditions for throughput, cost reduction, and waste minimization.
  • Collaborate with process engineers to modify and adapt equipment for scale-up.


Technical Documentation & Compliance

  • Prepare process development reports, scale-up protocols, and technical transfer documents.
  • Ensure compliance with GMP, safety, and environmental regulations.
  • Maintain detailed experimental records and batch manufacturing instructions.
  • Support regulatory filings by providing technical data and process descriptions.


Cross-Functional Collaboration

  • Work closely with R&D chemists, analytical teams, production, and quality control.
  • Liaise with procurement and vendors for catalyst raw materials and equipment.
  • Provide technical training to production teams on catalyst handling and process parameters.

Qualifications


  • Master’s or Ph.D. in Chemistry, Chemical Engineering, or related field, with specialization in catalysis or process chemistry.
  • 7+ years of experience in catalyst development, preferably in a pharmaceutical or fine chemical manufacturing environment.
  • Proven track record of taking catalytic processes from lab concept to commercial scale.
  • Strong understanding of chemical kinetics, reactor design, and process safety.
  • Familiarity with GMP, ICH guidelines, and regulatory requirements for pharmaceutical manufacturing.


Required Skills


  • Deep knowledge of homogeneous/heterogeneous catalysis, metal complexes, and enzyme catalysis.
  • Strong problem-solving skills for troubleshooting process deviations.
  • Proficiency in analytical techniques (GC, HPLC, ICP-MS, XRD, BET surface analysis, etc.).
  • Ability to lead cross-functional technical teams.
  • Excellent technical writing and presentation skills.


Preferred Skills


  • Experience in a lab and pilot plant environment with periodic visits to production facilities.
  • Exposure to chemicals and equipment; adherence to strict safety protocols required.

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