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Overview

Reporting directly to the Senior Director of Quality, the Quality Engineer is tasked with enhancing quality systems by utilizing data-driven analysis, conducting risk evaluations, supporting validation efforts, and investigating root causes. This role requires close collaboration across departments including QA, QC, Manufacturing, Engineering, and Operations to boost process capabilities, mitigate quality risks, and maintain compliance in a regulated production setting.

About Us

Since its establishment in 2010 near Austin, Goodkind has become a pioneer in producing eco-friendly personal care and beauty products, with expertise in natural deodorant, skincare, and facial care. The company adheres to multiple consumer and retailer standards, such as Ecocert, EWG, Credo, and Sephora. As a Certified B Corporation, Goodkind integrates social and environmental considerations into its business values, aiming to generate benefits for associates, customers, suppliers, communities, and the environment alike.

Key Responsibilities

Lead and assist in root cause analyses for deviations, non-conformance reports (NCRs), corrective and preventive actions (CAPA), and process defects
Examine quality and manufacturing data sets to recognize trends, recurring problems, and potential improvements
Support the implementation of CAPA and verify their effectiveness
Conduct risk assessments concerning manufacturing operations, quality incidents, and process modifications
Assist with validation projects including process validations, equipment qualifications, and cleaning validations
Collaborate with teams from Manufacturing, QA, QC, and Engineering to enhance process performance and operational efficiency
Develop quality metrics, trend analyses, and support continuous improvement efforts
Engage in change control activities assessing impacts on processes and quality
Contribute to refining procedures, workflows, and quality documentation
Participate in internal audits, regulatory inspection preparations, and compliance support
Drive data-centric process enhancements and risk control strategies
Perform additional related tasks as required

Requirements

Bachelor's degree in Engineering, Chemistry, Life Sciences, or a closely related scientific discipline
Minimum of three years' experience in Quality Engineering, Quality Systems, Manufacturing Engineering, or Quality Assurance within regulated manufacturing sectors
Comprehensive understanding of Good Manufacturing Practices (GMP) and quality compliance systems
Proficiency in root cause investigations, CAPA, deviation management, and change control procedures
Experience supporting validation tasks and performing risk evaluations
Strong analytical, problem-solving, and organizational capabilities
Capacity to analyze and detect data trends for process enhancement
Excellent written and oral communication skills
Ability to manage various projects and priorities in a dynamic environment

Preferred Qualifications

Background in over-the-counter (OTC), pharmaceutical, cosmetic, or personal care manufacturing
Experience with validation protocols and equipment qualification efforts
Familiarity with electronic Quality Management Systems (eQMS), ERP platforms, and manufacturing data software
Knowledge of Lean Manufacturing, Six Sigma, or other continuous improvement frameworks
Audit and regulatory inspection support experience
Understanding data integrity principles and risk management tools such as FMEA, 5 Whys, and Fishbone diagrams

Key Skills and Competencies

Root cause analysis and problem-solving
Risk assessment and mitigation
Data analytics and trend identification
Process optimization and continuous improvement techniques
Expertise in validation and quality systems
Effective cross-functional teamwork and communication
Strong organizational and project oversight skills
Technical writing and documentation capability
Critical thinking and informed decision-making
Accountability and proactive ownership

Quality Engineer

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