Quality Assurance Supervisor
Garonit Pharmaceutical
Quality Assurance Supervisor
Garonit Pharmaceutical
Global API manufacturer for pharmaceutical ingredients
Quality Assurance Supervisor
Location: Fairfield & Flanders, NJ
Garonit Pharmaceutical is seeking an experienced, hands-on Quality Assurance Supervisor to join our growing Quality team, supporting operations at both our Fairfield and Flanders, New Jersey facilities. This role will oversee daily Quality Assurance activities, support the development and maintenance of our Quality Management System (QMS), ensure compliance with current Good Manufacturing Practices (cGMP), and drive continuous improvement initiatives across both sites.
Key Responsibilities
Qualifications
Compensation & Benefits
The anticipated salary range for this position is $90,000–$120,000 per year. Actual compensation will be determined based on factors such as experience, qualifications, skills, and other job-related considerations. This position is also eligible for consideration for a discretionary year-end bonus, based on Company and individual performance. Any bonus is discretionary and is not guaranteed.
Garonit Pharmaceutical offers eligible employees a benefits package that includes medical, dental, and vision insurance; a 401(k) retirement plan with Company match; paid time off (PTO); paid holidays; and other benefits in accordance with applicable Company plans and policies.
About The Role
This is a full-time, onsite position supporting both our Fairfield and Flanders, New Jersey facilities. The Quality Assurance Supervisor will play a key role in overseeing daily QA operations, maintaining compliant quality systems, supporting regulatory inspection readiness, and driving continuous improvement across our pharmaceutical manufacturing operations. Regular travel between both facilities will be required.
Equal Employment Opportunity
Garonit Pharmaceutical is an equal opportunity employer. We consider qualified applicants for employment without regard to race, color, religion, sex, pregnancy, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local law.
Global API manufacturer for pharmaceutical ingredients
Garonit Pharmaceutical produces Active Pharmaceutical Ingredients, especially Chlorhexidine Gluconate, for global pharmaceutical customers. It uses a vertically integrated model from intermediates to finished dosage forms with cGMP/WHO-GMP facilities in the US and India and distribution warehouses in Europe. It plans a 200,000-square-foot New Windsor facility to become the world’s largest Chlorhexidine Gluconate producer, supported by New York state grants and including an R&D center for FDA-regulated products. With certifications from US FDA, EDQM, and PMDA, it competes on scale, end-to-end manufacturing, and global reach, aiming to supply large-scale, compliant Chlorhexidine Gluconate worldwide while expanding U.S. operations and developing FDA-regulated formulations.
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