Quality Research Associate

This Jobot Job is hosted by: Juan CorreaAre you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume.Salary: $75,000 - $90,000 per year

A bit about us:We are a San Diego based Contract Research Organization that delivers GLP and Non-GLP biological services to clients in pharmaceutical/biopharmaceutical, biotech, academic research, medical device and related industries since 2001. With a foundation premised on compliance, regulations adherence and the art of execution under the know-how of anatomical, pharmacological, safety evaluations and rapid learning. Some of our expertise includes the core areas of in vitro and in vivo research, Academic Research, Model Development, multi-project handling and proficient Study Directorship.

Why join us?A great working culture that genuinely cares and wants to see you grow, and whose leaders are continually sharing their knowledge and experience. We encourage growth, and present a great career path for the earnest and capable, without the limitations found in other places. Our team takes pride in being a reliable service provider, and continually seeks opportunities to grow in quality and efficiency in areas we serve Come grow with us!Full time position with a competitive base salary.Great benefit package after successful completion of 90-day probationary period.Health & Dental401KPaid Time-OffAbove all a positive supportive company environment.Must be eligible for work in the United States of America.

Job DetailsThe duties presented are only a summary of duties. The Quality Research Associate professionals serve as key members of the Compliance Team and activities in all of our facilities therefore a individuals of high integrity. In general the QRA I ensure compliance with company policies, SOP's, GLP, quality assurance program, safety and environmental standards, and regulatory agencies (i.e. FDA, DEA, San Diego County, EPA, OSHA).Duties & Responsibilities include:GLP Compliance (as a member of the Quality Assurance Unit)Review non-clinical study protocols (GLP and non-GLP).Perform critical phase audits, raw data audits and final report review for GLP studies.Ensure personnel are trained and qualified prior to participation in GLP study.Support in the facility inspections to ensure GLP compliance.Maintain the SOP and Forms systems, including review, revisions issuance, and intranet uploads.Create and modify documents (SOPs, Forms) using Microsoft Office.Perform Quality Control on study specimens and samples prior to shipment.Assist in investigating and closing CAPAs.Ensure non-clinical studies are archived in a timely manner.Equipment ManagementMaintains Asset Inventory List.Assigns asset numbers to all incoming equipment.Ensures that the asset numbers have equipment files and calibration logs.Ensures that equipment is calibrated as scheduled and needed.Support validation activities as needed.Knowledge, Experience & EducationBachelor of Science or college degree.A minimum of 2 years' experience in animal research regulations and especially in GLP.Well versed with regulations in U.S. and other regulatory requirements.Sound reasoning ability to prioritize, act and effectively work with other departments.Able to multi-task and execute with precise attention to detail.Good record keeping and attention to detail essential.Must be proficient with computers and software such as Microsoft Word and Excel.Excellent communication skills are a must; Good organizational and problem-solving skillsInterested in hearing more? Easy Apply now by clicking the "Apply Now" button.