GLP Quality Assurance Specialist
Listed on 2026-06-27
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Engineering
Scientist II in Global Stewardship / Regulatory
Clorox is the place that's committed to growth – for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact on consumers, communities, and teammates. Join our team. #Clorox Is The Place
Your role at Clorox:
As a Scientist II in Global Stewardship / Regulatory, you will be part of the Quality Assurance Unit (QAU) with responsibility for Good Laboratory Practice (GLP), working with a cross functional team to generate quality data and documentation for business critical Regulatory submissions to the US Environmental Protection Agency (EPA). This critical work is a key driver for delivering Cleaning Business objectives and enables health of the Cleaning Business.
In this role, you will:
- Program Management
- Collaborate within the QAU and with GLP staff to develop and implement improvements for overall test facility compliance
- Provide input to management via quarterly updates
- Auditing
- Be responsible for the inspection of protocols, in-process testing, data/draft reports, final reports
- Coordinate CPC annual facility self-assessment and contract labs inspections. Communicate observations and implement changes as needed
- Identify and drive improvements and efficiencies within the auditing process
- Training/Guidance
- Lead training for GLP personnel
- Provide guidance on GLP regulations/requirements for each GLP study as needed
- Improve training materials and experience to better prepare users for GLP
- Study-Specific Activities (excluding auditing)
- Define studies and set timing with GLP product team members
- Review draft protocols, deviations, amendments, and study notes and provide input and guidance on format/content
- Generate and distribute inspection reports to Study Director & management
- Review revised data/report to ensure all audit findings are appropriately addressed
- Sign final report QA statement
- Identify, develop and champion improvements to study-specific activities
- Other
- Represent Clorox during EPA inspections
- Monitor and implement new processes to address changes in regulations or internal practices
- Interact w/ contract laboratories on QA/GLP issues
- Update and issue Master Schedule
- Review and provide input on draft SOPs
- Maintain QAU files
- Seek to continuously find opportunities to improve GLP activities
What we look for:
- Bachelor or Masters degree in Chemistry or other related Science discipline or a Quality-oriented education.
- 2-4 years laboratory, quality or plant work experience
- Analytical skills and knowledge
- Good Laboratory Practice (GLP) or Good Manufacturing Process (GMP) experience
- Desired:
- Knowledge of 40 CFR Part 160 regulations, analytical techniques (including, but not limited to, manual titration, LC and GC), familiarity with CPG product development, micro and toxicity testing is desired.
Skills & Abilities:
- Strategic thinking and ability to increase the quality-consciousness of employees by your persuasiveness
- Customer and quality focused, team spirit and integrity
- Experience representing GLP compliance in a cross-functional team setting and project management experience
- Ability to understand and interpret GLP regulations and technical documents
- Ability to work independently and collaboratively in a fast-paced, cross-functional team environment
- Effectively manage multiple priorities; results-oriented; process-driven
- High attention to detail
- Flexible and adaptable to changing business needs and priorities
- Strong oral and written communication skills with ability to engage and influence various audiences at multiple levels in the organization
- Excellent planning, organizational, and time management skills with attention to detail
- Some travel may be required (approximately 5%)
Workplace type:
This position will be located in our Pleasanton, CA office, and the individual will be expected to be in the office of 3 days a week.
Our values-based culture connects to our purpose and empowers people to be their best, professionally and personally. We serve a diverse consumer base which is why we believe teams that reflect our consumers bring fresh perspectives, drive innovation, and help…
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