The Quality Assurance Consultant will oversee all GLP studies to ensure compliance with the standard procedures and specific protocols so that no deviations occur without proper authorization. He or she will report significant problems that are likely to affect the integrity of a study to the Study Director and management.
Candidates must show attention to detail, have excellent communication skills and be able to work within a team under challenging and sometimes stressful conditions. Candidates should have an exceptional knowledge of commonly-used QA concepts, practices, and procedures within GLP (FDA Regulated) field. The QA Consultant is responsible for improving the organization’s knowledge base of current QA regulations and for informing Management of any new and/or revised regulations. Candidates must have above average communication skills (writing and speaking) and be responsible for supporting a healthy working environment between other functions where QA is concerned. May oversee personnel engaged in QA support activities. Perform other assigned duties as necessary.
EDUCATION/ EXPERIENCE Prefer the individual have a Bachelor’s degree or above in a biology related field. Knowledge of Good Laboratory Practices is required. Good communication skills and the ability to speak with technical personnel about studies will be required. Extreme attention to detail and exceptional grammar skills is preferred.
Compensation will be commensurate with experience
Job Type: Contract
Salary: $25.00 -$50 /hour
Job Location:
•Fort Collins, CO
Required education:
•Bachelor's