What are the responsibilities and job description for the Quality Control Supervisor position at Garonit Pharmaceutical?
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.