About this role
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.
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.
About Garonit Pharmaceutical
Garonit Pharmaceutical is hiring for the qc supervisor role. NewJob aggregates active openings directly from Garonit Pharmaceutical's applicant tracking system, so this listing is current.
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