QC Supervisor

QC Supervisor

Onsite in Fairfield, NJ

We’re looking for a QC Supervisor who’s both a hands-on technical expert and a strong leader. This role manages the daily operations of our QC Laboratory - leading testing, method development, and data review while ensuring full cGMP compliance.

 What You’ll Do

• 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.


• Manage and schedule lab workloads to meet production timelines.


• Ensure lab safety, data integrity, and adherence to FDA and ICH guidelines.


• Collaborate cross-functionally to resolve quality-related issues quickly.


• Develop and mentor QC staff through training and performance development.


• Support continuous improvement initiatives to enhance compliance and efficiency.

 What You’ll Bring

• Bachelor’s degree in Chemistry or a related scientific field.


• 2+ years in a supervisory or management role in a pharmaceutical QC lab.


• Strong experience with Empower 3, HPLC, GC, and wet chemistry.


• Deep understanding of cGMP, ICH, CFR, and USP testing requirements.


• Experience in method development, validation, and stability testing.


• Proven leadership, training, and coaching skills.


• Excellent problem-solving, documentation, and communication abilities.


• High attention to detail, strong work ethic, and commitment to quality.

 Why Garonit Pharma

• Work with cutting-edge equipment in a collaborative, growth-oriented environment.


• Play a key role in ensuring product quality and regulatory success.


• Competitive compensation and career growth opportunities.