About this opportunity
The Goodkind Co. lists this Quality Assurance Supervisor opportunity in round rock, Texas. Review the employer’s description below for duties, qualifications and application requirements.
Job description
QA SupervisorReporting to the QA Manager, the QA Supervisor is responsible for coordinating daily Quality Assurance operations and supervising QA personnel to ensure compliance with internal procedures, Good Manufacturing Practices (GMP), and regulatory requirements. This role supports implementation and execution of Quality System processes through team leadership, workflow coordination, training oversight, and operational compliance activities.The QA Supervisor serves as a frontline quality leader, ensuring consistent execution of QA processes, timely follow-up of quality events, and effective communication between QA, Manufacturing, QC, and other departments.Founded in 2010 and based in the Austin area, Goodkind is a leading manufacturer of clean and green personal care and beauty products. Goodkind specializes in natural deodorant, skincare, and facial care products. The company has a wealth of experience in the formulation of these products and can develop according to a variety of guidelines from consumer organizations such as Ecocert to EWG, to retailers such as Credo or Sephora.Goodkind is a certified B Corporation. As such, we balance purpose and profit, considering the impact of decisions across associates, customers, suppliers, community, and the environment. Goodkind believes by following this central multi-stakeholder approach, we are creating optimal value for each stakeholder while leaving the world a better place.Supervise day-to-day QA activities and provide guidance, training, and support to QA team membersCoordinate QA workflow to ensure timely completion of quality-related activities and documentationSupport batch creation, as well as, record review activities for completeness and compliance with established proceduresAssist with the initiation, tracking, and follow-up of deviations, NCRs, CAPA, and change control recordsSupport investigations and root cause analysis activities in collaboration with QA and cross-functional teamsReview quality documentation, SOPs, and work instructions for accuracy and complianceSupport material review and disposition activities in coordination with QA leadershipAssist with validation and qualification activities, including protocol execution and documentation reviewMaintain oversight of calibration tracking and compliance statusSupport internal audits, inspections, and audit readiness activitiesTrack and report quality metrics and follow-up itemsCollaborate cross-functionally with Manufacturing, QC, Engineering, and Operations teamsEnsure training compliance and onboarding of QA personnelPerform additional duties as assigned
Worksite address
round rock, TX, 78664, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.