About this opportunity
The Goodkind Co lists this Senior Chemist / Laboratory Supervisor opportunity in round rock, Texas. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Overview
Reporting to the Senior Director of Quality, the Senior Chemist / Laboratory Supervisor is responsible for providing technical and operational leadership for the Quality Control Laboratory within a regulated manufacturing environment. This role oversees daily laboratory operations while driving improvements in GMP compliance, laboratory systems, analytical practices, and overall laboratory effectiveness.
The position serves as the technical lead for laboratory investigations, method development, method validation, and implementation of scientifically sound laboratory controls. This role is also responsible for strengthening laboratory compliance practices, improving data integrity, standardizing laboratory processes, and supporting the development of a scalable QC laboratory operation capable of supporting OTC product manufacturing and regulatory expectations.
In addition to technical responsibilities, the Senior Chemist / Laboratory Supervisor provides leadership and oversight for QC laboratory personnel, ensuring proper training, workload coordination, and execution of laboratory activities in accordance with GMP and internal quality standards.
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
Lead daily QC laboratory operations and supervise laboratory personnel
Establish and strengthen GMP laboratory practices, controls, and documentation standards
Develop, qualify, validate, and improve analytical test methods and laboratory procedures
Lead laboratory investigations related to OOS, atypical results, deviations, and nonconformances
Review laboratory data, test results, and analytical documentation for accuracy, reliability, and compliance
Ensure proper calibration, maintenance, and qualification of laboratory equipment and instruments
Support implementation and oversight of laboratory data integrity practices
Develop and improve laboratory SOPs, specifications, test methods, and related documentation
Coordinate laboratory scheduling, testing priorities, and resource planning
Partner cross-functionally with QA, Manufacturing, R&D, and Operations to support product quality and process improvements
Support validation activities, including method validation, equipment qualification, and stability-related activities as applicable
Train and mentor laboratory staff on GMP requirements, laboratory techniques, and compliance expectations
Support audit readiness activities, regulatory inspections, and internal audits
Identify and implement continuous improvement initiatives to improve laboratory efficiency, compliance, and technical capability
Perform additional duties as assigned
What We Require
Bachelor’s degree in Chemistry, Biochemistry, or related scientific discipline
5+ years of laboratory experience in a regulated manufacturing environment
Strong working knowledge of GMP requirements and laboratory compliance expectations
Experience interpreting FDA OTC Monographs and USP test methods
Experience with analytical method development, qualification, and validation
Experience leading laboratory investigations, root cause analysis, and corrective actions
Experience supervising or leading laboratory personnel
Strong understanding of laboratory instrumentation, calibration, and data integrity principles
Strong technical writing, analytical, and organizational skills
Ability to manage multiple priorities in a fast-paced environment
Preferred Qualifications
Experience in OTC, pharmaceutical, cosmetic, or personal care manufacturing
Experience supporting FDA inspections and regulatory audits
Familiarity with ISO standards and laboratory quality systems
Experience with stability programs and specification management
Experience with ERP systems, LIMS, or electronic quality systems
Knowledge of risk assessment and continuous improvement methodologies
Key Skills & Competencies
GMP laboratory operations and compliance
Analytical method development and validation
Laboratory investigations and root cause analysis
Leadership and team development
Data integrity and technical documentation
Laboratory equipment qualification and calibration oversight
Problem-solving and critical thinking
Cross-functional collaboration and communication
Organizational and workload management
Continuous improvement mindset
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Worksite address
round rock, TX, 78682, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.