Analytical Research And Development Analyst

3 days ago

Lucknow, Uttar Pradesh, India TAPI Full time ₹ 15,00,000 - ₹ 25,00,000 per year

Company Description

At TAPI, we're not just a company—we're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide.

Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives.

Job Description

We are seeking an experienced analytical scientist to support method development, validation, and technology transfer activities for pharmaceutical products. The role involves close collaboration with chemical research teams and production sites to ensure analytical excellence and regulatory compliance.

Key Responsibilities:

  • Develop analytical methods for in-process materials, raw materials, intermediates, and finished products
  • Conduct carryover studies for reagents and genotoxic impurities
  • Perform method validation, equipment cleaning validation, and stability analysis
  • Characterize and isolate impurities and support technology transfer to production
  • Prepare specifications, standard test procedures (STPs), and qualification protocols
  • Provide analytical support to chemical research teams for process development and optimization
  • Maintain the analytical laboratory in compliance with GLP and safety standards
  • Ensure proper documentation in lab notebooks and equipment records as per SOPs
  • Oversee calibration and maintenance of laboratory equipment and consumables

Desired Skills:

  • Strong understanding of analytical method development and validation practices
  • Familiarity with GLP, safety protocols, and regulatory documentation standards
  • Ability to work collaboratively with cross-functional teams
  • Attention to detail, organizational skills, and a proactive approach to problem-solving

Qualifications

The ideal candidate will have:

  • M.Sc. in Chemistry or M.Pharm with a minimum of 5 years of industrial experience
  • Ph.D. in a relevant field with at least 2 years of experience

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