Are you ready to take your career in pharmaceutical research and development to the next level? Teva Pharmaceuticals is seeking a dedicated Analytical R&D Analyst I to join our team at our cutting-edge facility in Gwalior, India. This role is ideal for individuals with expertise in analytical chemistry and a passion for making a positive impact in the pharmaceutical industry.
Who We Are: Leading the API Industry
Teva Active Pharmaceutical Ingredients (TAPI) is a renowned international supplier of active pharmaceutical ingredients (APIs) with a robust portfolio featuring over 350 API products. For over 80 years, we’ve served as a trusted partner to 80% of the top 50 global pharmaceutical companies. Our long-standing history in the generic API industry underlines our commitment to quality, innovation, and exceptional customer service.
With more than 4,000 professionals across 14 global sites, including our state-of-the-art production facilities in countries like Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India, TAPI continues to invest significantly in research and development. This ongoing commitment ensures that we can deliver timely and effective solutions to our clients and the broader healthcare community.
Your Role: Responsibilities and Daily Activities
As an Analytical R&D Analyst I, your primary responsibilities will include:
- Method Development: You will be integral in developing analytical methods and providing routine analytical support for pilot projects, raw materials, intermediates, and drug substances.
- Instrument Proficiency: Your expertise in various analytical techniques, including HPLC, UPLC, GC, GC-MS, FTIR, PSD, TGA, KF, and Auto titrators, will be crucial for conducting stability studies and forced degradation studies in compliance with ICH guidelines.
- Instrument Calibration and Maintenance: You will ensure the calibration and maintenance of sophisticated instruments such as balances, HPLC, GC, IR, and melting point analyzers.
- Documentation and Compliance: Adhering to GMP requirements, you will document all experiments and analyses thoroughly and maintain compliance in data recording and laboratory practices.
- Collaboration: You will work closely with quality control (QC) teams during validation batches and contribute to regulatory tasks related to both commercial and pipeline products as required.
- Safety and GLP: Ensuring a safe laboratory environment while upholding GLP and safety requirements is a key aspect of your role.
- Continuous Learning: Participating in departmental trainings and discussions will help you stay updated with the latest advancements and methodologies in analytical chemistry.
Qualifications and Experience Required
To thrive in this role, you will need:
- A Master’s Degree (MSc) in Organic Chemistry or Analytical Chemistry.
- 3 to 5 years of relevant work experience in the field of analytical chemistry, preferably within the pharmaceutical industry.
