Redica Systems is a forward-thinking technology company leveraging data, analytics, and expertise to deliver meaningful insights to quality and safety professionals around the world. By applying artificial intelligence to large and disparate government data sets, Redica Systems empowers our customers to improve compliance, increase product quality, and build a more efficient organization.
We serve life science customers in the pharmaceutical, medical device, and food industries, including 19 of the top 20 pharmaceutical companies and 9 of the 10 top medical device companies.
Headquartered in Pleasanton, CA, we’re open to remote work for candidates residing in the US. Let's talk!
We’re looking for a curious, team-oriented, data connoisseur with a passion for getting stuff done. Your primary role is shaping and participating in proactive global monitoring and surveillance activities of the full drug development lifecycle in support of our suite of regulatory and compliance intel products and services.
This is an ideal role for someone interested in taking their hard-won knowledge and experience in the Life Science industry and applying it in a new and groundbreaking way. For the right person, this role could be shaped to accommodate a 3 - 4 day work-week.
Top Pharmaceutical Companies, Food Manufacturers, Medical Device Companies, and Service firms from around the globe rely on Redica Systems to mine and process government inspection, enforcement, and registration data in order to quantify risk signals about their suppliers, identify market opportunities, benchmark against their peers, and prepare for the latest inspection trends. Our data and analytics have been cited by major media outlets such as MSNBC, WSJ, and the Boston Globe.
Redica Systems is an equal opportunity employer. We welcome and encourage diversity in the workplace regardless of race, gender, religion, age, sexual orientation, disability, or veteran status.
All your information will be kept confidential according to EEO guidelines.
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