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QC Supervisor at Garonit Pharmaceutical - ApplyBlast

QC Supervisor

Garonit Pharmaceutical

4 months ago

Fairfield, NJ

Onsite

Full Time

Senior

2 applicants

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About this role

A QC Supervisor at Garonit Pharma oversees the daily operations of the QC Laboratory, leading testing, method development, and data review while ensuring cGMP compliance.

Responsibilities

Supervise and lead a team of QC chemists and analysts
Oversee all analytical testing for manufacturing, release, and stability
Review and interpret HPLC, GC, and wet chemistry data in compliance with cGMP
Author and review SOPs, analytical methods, and validation protocols
Conduct and support laboratory investigations, CAPA, and change controls

Skills

Qualifications

Bachelor’s degree in Chemistry or related scientific field2+ years in a supervisory or management role in a pharmaceutical QC labExperience with Empower 3, HPLC, GC, and wet chemistryDeep understanding of cGMP, ICH, CFR, and USP testing requirementsExperience in method development, validation, and stability testing

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.