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.