Reporting 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.
About Us
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.
What You’ll Do
Supervise day-to-day QA activities and provide guidance, training, and support to QA team members
Coordinate QA workflow to ensure timely completion of quality-related activities and documentation
Support batch creation, as well as, record review activities for completeness and compliance with established procedures
Assist with the initiation, tracking, and follow-up of deviations, NCRs, CAPA, and change control records
Support investigations and root cause analysis activities in collaboration with QA and cross-functional teams
Review quality documentation, SOPs, and work instructions for accuracy and compliance
Support material review and disposition activities in coordination with QA leadership
Assist with validation and qualification activities, including protocol execution and documentation review
Maintain oversight of calibration tracking and compliance status
Support internal audits, inspections, and audit readiness activities
Track and report quality metrics and follow-up items
Collaborate cross-functionally with Manufacturing, QC, Engineering, and Operations teams
Ensure training compliance and onboarding of QA personnel
Perform additional duties as assigned
Requirements
What We Require
Bachelor’s degree in Life Sciences, Chemistry, Engineering, or related field (or equivalent experience)
5+ years of Quality Assurance experience in a regulated manufacturing environment
2+ years of leadership, lead, or supervisory experience preferred
Experience coordinating quality system activities and supporting cross-functional quality initiatives
Strong knowledge of GMP requirements and quality systems
Experience supporting deviations, NCRs, CAPA, and change control processes
Experience reviewing quality documentation and batch records
Strong organizational, communication, and documentation skills
Ability to manage multiple priorities in a fast-paced environment
Preferred Qualifications
Experience in OTC, pharmaceutical, cosmetic, or personal care manufacturing
Experience supporting audits and regulatory inspections
Familiarity with eQMS systems and document control processes
Knowledge of validation and calibration programs
Understanding of data integrity principles and risk-based quality systems
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