About the Company
Naari Pharma is a B2B pharmaceutical company dedicated exclusively to advancing women’s health. With a sharp focus on hormonal therapies, we manufacture high-quality finished dosage forms for global markets. Our products are present in over 60 countries, including key regulated territories such as the US, Canada, Europe, and Australia. Backed by a state-of-the-art R&D and manufacturing facility in Rudrapur, Uttarakhand, our global operations are seamlessly driven from offices in Bangalore, Noida, Singapore, and the United States.
Responsibilities
- Interpret results, evaluate data, draw conclusions, and handle complex tasks without predefined procedures.
- Approve protocols, reports, and scientific documents; support registration documentation and liaise with authorities.
- Lead analytical method development and validation for APIs, including assay, related substances, residual solvents, and PSD.
- Manage in-process and stability sample releases, adhering to GLP, GMP, USFDA, and ICH regulatory guidelines.
- Maintain laboratory records, ensure calibration of instruments, and manage chemical inventory effectively.
- Hands-on experience with HPLC, UPLC, GC, Ion Chromatography, IR, KF, and Particle Size Analysers.
- Foster a safe laboratory environment, ensure adherence to safety practices, and minimize laboratory failures.
- Stay updated on new analytical techniques and regulatory requirements while maintaining world-class ARD systems.
- Should have 15 to 18 years' experience into ARD leading the entire ARD team
Qualifications
MSc
Location
Who are ready to relocate to Rudrapur location.