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GLP Study Director 1326812 A leading consumer products company is seeking a GLP Study Director. The successful candidate will lead and manage Good Laboratory Practice (GLP) studies and will work directly with cross-functional teams to generate quality data and documentation for business-critical regulatory submissions to the US Environmental Protection Agency (EPA). The ideal candidate has 5+ years working in a Laboratory. The company offers a great work environment! GLP Study Director Pay and Benefits: • Hourly pay: $30/hr • Worksite: Leading consumer products company (Pleasanton, CA 94588 - Onsite) • W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL • 40 hours/week, 3-4 Month Assignment with a possibility to extend. GLP Study Director Responsibilities: • Maintain lab documentation following Standard Operating Procedures (SOP’s) to ensure GLP compliance. • Maintain and calibrate lab equipment at required intervals to ensure GLP compliance. • Ensure laboratory supplies are available and the laboratory is a safe environment for all employees. • Provide training or approvals for scientists (or others) to enter the GLP labs. • Leads all aspects of studies to ensure data accuracy and report quality: • Develop study protocols that meet technical, project and regulatory objectives. • Ensure that all GLP regulations are communicated to study participants and are strictly observed. • Work independently and collaboratively with the GLP Team to execute GLP studies, design experiments and safely complete assigned tasks in a timely manner. • Collaboratively work with the GLP Team to maintain well-organized supporting data files suitable for internal and external auditing. • Complete final reports and archive studies per GLP guidelines. • Ensures product availability, quality, sample transfers and tracking: • Prepare batches with appropriate documentation and tracking for GLP studies. • Conduct testing on batches to ensure quality and generate accurate GLP data for EPA submissions. Testing includes (but is not limited to) pH, titrations, density, physical characteristics, etc. • Review analytical data and prepare final study reports, taking responsibility for accuracy and compliance. • Prepare and coordinate testing and transfer requirements with other functions. GLP Study Director Qualifications: • 5+ years working in a laboratory desired. • 1+ year experience working in a laboratory with product formulation and/or analytical lab experience. • Associate’s or Bachelor's degree in Chemistry or other related Science discipline, or greater than 2 years of college courses in chemistry or other related science discipline. • Good Laboratory Practice (GLP) or Good Manufacturing Process (GMP) experience desired. • Experience working on EPA regulated products desired. • Ability to act as Project Manager of GLP Studies. • Excellent written, oral communication. • High attention to detail. • Excellent organizational, prioritization and decision-making skills. • Ability to work independently and as part of a team. • Push for results with a desire to learn. • Computer skills including Word and Excel. • Self-motivation, adaptability and multi-tasking skills. • Ability to follow SOP’s and accurate record-keeping skills.