QA Supervisor Position Available In Suffolk, New York

Job Title:

QA Supervisor Job Description The QA Supervisor will perform and coordinate the daily activities of the QA team, ensuring the release of products and generating Certificates of Analysis (CofAs). The role involves ensuring adherence to quality standards such as ISO, GMP, HACCP, and GFSI, and developing, implementing, and maintaining quality procedures, policies, and documentation. The QA Supervisor will conduct root cause analyses and implement corrective and preventive actions (CAPA), coordinate internal audits, and support external audits, both regulatory and client-based. Monitoring and reporting on key quality metrics, such as defect rates, non-conformances, and customer complaints, is essential. The position also requires training and mentoring QA staff on quality standards, SOPs, and best practices, as well as collaborating with production, engineering, and QC teams to resolve quality issues. Supporting quality improvement projects, maintaining accurate QA records, and ensuring proper documentation of inspections and findings are critical aspects of this role. Responsibilities Perform and coordinate daily activities of the QA team. Ensure adherence to quality standards including ISO, GMP, HACCP, and GFSI. Develop, implement, and maintain quality procedures, policies, and documentation. Conduct root cause analyses and implement corrective and preventive actions (CAPA). Coordinate internal audits and support external audits. Monitor and report on key quality metrics. Train and mentor QA staff on quality standards, SOPs, and best practices. Collaborate with production, engineering, and QC teams to resolve quality issues. Support quality improvement projects. Maintain accurate QA records and ensure proper documentation. Maintain QMS for change control, customer complaints, and reviews. Essential Skills Experience in GMP and FDA regulated industry. Strong knowledge of quality assurance practices. Proficiency in SOP, CAPA, and document control. Ability to conduct quality checks and batch record reviews. Understanding of food safety regulations. Additional Skills & Qualifications 3-5 years of experience in a quality role. Experience in a chemical manufacturing environment. Work Environment The work environment is a chemical manufacturing lab with working hours from 8 am to 5:30 pm.