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Regulatory Affairs Project Lead at Garonit Pharmaceutical - ApplyBlast

Regulatory Affairs Project Lead

Garonit Pharmaceutical

6 months ago

Fairfield, NJ

Onsite

Full Time

Senior

0 applicants

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About this role

A Regulatory Affairs Project Lead at Garonit Pharmaceutical drives regulatory strategy and execution for product portfolio advancement, with a focus on ANDA submissions and lifecycle management.

Skills

Qualifications

Bachelor’s degree in Life Sciences or related field

About Garonit Pharmaceutical

garonitpharma.com

Headquarters

Mumbai, Maharashtra, India

Company Size

501-1000 employees

Founded

1994

View Profile

Garonit Pharmaceutical is a US-headquartered (Flanders, NJ) manufacturer and global supplier of active pharmaceutical ingredients, with a primary focus on Chlorhexidine Gluconate 20%. The company is one of the few manufacturers in North America to simultaneously hold US FDA DMF, CEP EDQM, and PMDA Japan DMF certifications for CHG 20%, and operates cGMP facilities in New Jersey and India. Garonit serves 500+ global pharmaceutical clients across six continents, with offices and warehouses spanning North America, Europe, and Asia.