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.

• →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.

• 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.

• 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.