Navitas Life Sciences is a leading global player in the pharmaceutical and life sciences sector, specializing in bioanalytical research, clinical trials, and regulatory compliance. With a strong emphasis on innovation and quality, Navitas Life Sciences provides end-to-end solutions in drug development, ensuring adherence to GLP, USFDA, and other regulatory guidelines.
Job Description
Key Responsibilities:
- Method Development & Validation: Design and validate bioanalytical methods using LCMS, HPLC, HPTLC, GC-MS, and other advanced instruments.
- Instrument Calibration: Perform routine calibration and maintenance of analytical instruments.
- Regulatory Compliance: Ensure adherence to GLP, USFDA guidelines, and maintain proper documentation.
- Team Coordination: Work collaboratively with cross-functional teams to improve Turn Around Time (TAT) and productivity.
- Quality Control: Monitor sample analysis, data integrity, and reporting to maintain high-quality standards.
Preferred Skills:
- Strong technical knowledge of LCMS, HPLC, GC-MS, and HPTLC.
- Familiarity with GLP, USFDA, and other regulatory guidelines.
- Excellent communication and interpersonal skills.
- Ability to manage workflows and enhance lab efficiency.
Eligibility Criteria
Education & Experience:
- UG: B.Pharma (Any Specialization)
- PG: M.Pharma (Any Specialization), M.Sc in Biotechnology/Chemistry
- Experience: 1-6 years in a Bioanalytical Lab
Job Type:
- Full-time, Permanent
- Location: Bengaluru / Manipal
- Openings: 8
Why Join Navitas Life Sciences?
✅ Work with cutting-edge bioanalytical instruments (LCMS, HPLC, GC-MS)
✅ Exposure to GLP & USFDA-compliant research
✅ Collaborative work environment with strong career growth
✅ Competitive salary & benefits
How to Apply?
If you are interested in this opportunity, please share your resume to- nagaraja.naik@navitaslifesciences.com