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Garonit Pharmaceutical

Global API manufacturer for pharmaceutical ingredients

Quality Assurance Supervisor

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree in Life Sciences, Chemistry, Pharmaceutical Sciences, or a related scientific discipline is required.
  • At least 5 years of Quality Assurance experience within pharmaceutical manufacturing or an FDA-regulated environment is required.
  • Strong knowledge of current Good Manufacturing Practices (cGMP), FDA regulations, 21 CFR Parts 210/211, and applicable International Council for Harmonisation (ICH) guidelines is required.
  • Hands-on experience with Quality Management Systems (QMS), deviations, Corrective and Preventive Actions (CAPAs), change controls, audits, and GMP documentation is required.
  • Experience supporting FDA inspections, regulatory audits, and inspection readiness activities is required.
  • Strong leadership, organizational, communication, and problem-solving skills are required.
  • Excellent attention to detail and the ability to manage multiple priorities in a fast-paced manufacturing environment are required.

Responsibilities

  • Supervise, train, and mentor Quality Assurance personnel, ensuring compliance with cGMP requirements and Company procedures.
  • Oversee daily QA operations across both facilities, including reviewing and approving SOPs, batch records, deviations, investigations, and other GMP documentation.
  • Maintain and continuously improve the Quality Management System in accordance with applicable regulatory requirements.
  • Manage and support deviations, investigations, CAPAs, and change controls.
  • Review and approve Certificates of Analysis and Certificates of Compliance, as authorized.
  • Support Annual Product Quality Reviews and monitor quality performance metrics.
  • Conduct internal audits and support FDA inspections, customer audits, and regulatory inspection readiness activities.
  • Support implementation and maintenance of electronic quality systems, including LIMS, TrackWise, and other electronic Quality Management System platforms.
  • Collaborate with Quality Control, Manufacturing, Operations, and other departments to investigate and resolve quality-related issues.
  • Identify opportunities for process improvements and implement effective quality initiatives across both facilities.
  • Promote a culture of quality, accountability, and continuous improvement throughout the organization.
  • Perform other related duties as assigned based on business and quality needs.

Desired Qualifications

  • Previous supervisory or team leadership experience is preferred.
  • Experience with LIMS, TrackWise, or other electronic quality management systems is preferred.

About the Company

Garonit Pharmaceutical

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.

Company size
11-50
Company stage
Not listed
Total funding
Not listed
Headquarters
Fairfield, NJ
Founded
1994

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