A Quality Assurance Supervisor supervises quality assurance staff and oversees processes involved in the prevention of faults in manufactured products and solutions.
Sunday - Thursday 11:15pm - 7:15am (Training would take place on 1st) Position Overview We are seeking a Quality Assurance Supervisor to oversee quality operations on our 3rd shift manufacturing team. This individual will play a critical role in ensuring compliance with FDA regulations, internal quality systems, and manufacturing standards while driving continuous improvement initiatives across the organization. The ideal candidate is a hands-on quality professional with strong leadership capabilities who thrives in a fast-paced manufacturing environment. This role requires someone who can effectively manage quality processes, mentor employees, enforce compliance standards, and foster a culture of accountability and continuous improvement. Key Responsibilities Supervise and support Quality Assurance personnel during 3rd shift operations Ensure compliance with FDA regulations, cGMP requirements, company policies, and internal quality standards Review and approve quality documentation, including batch records, deviations, non-conformances, and corrective actions Partner closely with Manufacturing, Operations, and other cross-functional teams to resolve quality-related issues Lead investigations related to deviations, non-conformances, and process exceptions Monitor production activities to ensure adherence to established procedures and quality requirements Drive continuous improvement initiatives focused on quality systems, compliance, efficiency, and employee engagement Coach, mentor, and develop team members through performance management, training, and ongoing feedback Address employee performance concerns, provide conflict resolution, and ensure compliance with company policies Support internal and external audits, inspections, and regulatory activities as needed Identify opportunities to strengthen quality systems and improve operational effectiveness Ensure SOPs remain current, accurate, and compliant with applicable regulations Required Qualifications 4-5+ years of experience within an FDA-regulated manufacturing or production environment Minimum of 3 years of Quality Assurance experience Experience reviewing and managing: SOPs Batch records Deviations Non-conformances Quality documentation Working knowledge of: FDA regulations cGMP requirements ISO standards Lean Manufacturing Principles Demonstrated success leading teams in a manufacturing or quality environment Experience managing employee performance, accountability, conflict resolution, and policy compliance Strong problem-solving, communication, and organizational skills Ability to make sound decisions in a dynamic manufacturing environment Preferred Qualifications Experience within the dietary supplement, nutraceutical, food, pharmaceutical, or related regulated manufacturing industries Previous supervisory or people leadership experience Experience driving process improvement initiatives and fostering a continuous improvement culture Familiarity with CAPA programs, audit support, and quality investigations Education Associate degree or bachelor's Degree in a scientific discipline preferred, including: Biology Chemistry Microbiology Food Science Biotechnology
