Teva Pharmaceuticals is a global leader in the manufacturing and development of generic medicines and innovative pharmaceutical solutions. Operating in nearly 60 countries, Teva is dedicated to making quality healthcare accessible to millions. As a prominent name on the World Health Organization’s Essential Medicines List, Teva’s products serve over 200 million people worldwide every day. Joining Teva means being part of a diverse and mission-driven team that aims to continually improve lives through affordable, effective healthcare solutions.
Job Opportunity: Analytical Researcher II
Teva Pharmaceuticals is seeking an experienced Analytical Researcher II to support its Global R&D sites, specifically focusing on projects related to Nitrosamines. This position is located in Ambernath, India, and offers an exciting opportunity to contribute to the development and validation of analytical methods in a dynamic environment.
Key Responsibilities
As an Analytical Researcher II, your primary duties will include:
- Execution of Analytical Tasks: Conduct method development, validation, and transfer activities for Nitrosamine impurities and other tests related to active pharmaceutical ingredients (API), intermediates, and finished products.
- Sample Handling: Manage and reconcile global analytical samples from Teva’s in-house and external sites.
- Data Compilation: Compile and document analytical data in compliance with Good Laboratory Practices (GLP) and quality systems.
- Laboratory Maintenance: Support the lab by ensuring the availability of columns, standards, chemicals, spares, and consumables.
- Documentation: Prepare Standard Test Procedures (STPs) and standard operating procedures (SOPs) related to analytical activities.
- Troubleshooting: Address and resolve issues related to analytical instruments.
- Calibration Activities: Perform daily instrument calibration to ensure consistent performance.
- Compliance: Maintain laboratory data integrity and uphold environmental, health, and safety (EHS) standards.
- Literature Research: Conduct searches to develop new analytical methods.
- Team Support: Collaborate effectively and adhere to GLP, quality compliance, and documentation practices.
Qualifications and Experience
Teva is looking for candidates who meet the following qualifications:
- Educational Background: M.Sc. in Analytical Chemistry, M.Pharm, or Ph.D. in a relevant field.
- Experience:
- Master’s degree holders: 6-9 years of relevant experience in analytical chemistry, with a focus on method development and validation for Nitrosamine impurities.
- Ph.D. holders: 3-6 years of experience.
- Technical Expertise: Hands-on experience with advanced mass spectrometry technology such as LCMSMS, GCMSMS, and LC-HRMS.
- Regulatory Knowledge: Familiarity with regulatory standards for various markets (US, EU, Canada) and pharmaceutical quality systems.
- ICH Guidelines: Sound knowledge of International Council for Harmonisation (ICH) guidelines.
Personal Attributes
The ideal candidate should possess:
- Communication Skills: Basic yet effective communication abilities and an aptitude for working within a matrix structure.
- Integrity and Trustworthiness: A strong ethical foundation.
- Cultural Awareness: Respect for diverse backgrounds and practices.
- Motivation: Self-driven with a proactive approach to tasks.
