GLP Study Director

CTG is seeking to fill a GLP Study Director opening for our client in Pleasanton CA.

Duration: 3 months, with the potential to extend

Location: Pleasanton, CA

Overview:

     As GLP Study Director, you will have overall responsibility for the technical conduct of GLP studies. You would be the principal point of study control for activities related to compliance for studies, collaborating with Clorox employees across Product Development, Microbiology, Toxicology, Analytical and Global Stewardship.

GLP Studies of responsibility include Characterization to support Microbiological and Toxicology testing, Physical Chemistry and Storage Stability/Corrosion testing. 

Key Responsibilities:

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 incudes (but 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 

Requirements:

• 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
• At least 1 year experience working in a laboratory with product formulation and/or analytical lab experience

Desired:

• 5+ years working in a Laboratory
• Good Laboratory Practice (GLP) or Good Manufacturing Process (GMP) experience
• Experience working on EPA regulated products

Minimum:

• 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 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

Excellent verbal and written English communication skills and the ability to interact professionally with a diverse group are required.

CTG does not accept unsolicited resumes from headhunters, recruitment agencies, or fee-based recruitment services for this role.

To Apply:

To be considered, please apply directly to this requisition using the link provided. For additional information, please contact Laura Dominguez at 716-887-7203 or Laura.Dominguez@ctg.com. Kindly forward this to any other interested parties—thank you!

The expected base salary for this position ranges from $30.45 to $32.62 per hour.  Salary offers are based on a wide range of factors including relevant skills, training, experience, education, market factors, and where applicable, licensure or certifications obtained. In addition to salary, a competitive benefit package is also offered.