Redica Systems is a data and analytics SaaS platform that helps regulated industries improve their quality and stay on top of evolving regulations. We are shaping the future of predictive quality with our pioneering work in AI workflows and the development of an exclusive intelligence layer for quality and regulatory data. Our purpose-built processes transform one of the industry’s most complete data sets—aggregated from hundreds of health agencies and unique Freedom of Information Act (FOIA) sourcing—into meaningful answers and insights that reduce regulatory and compliance risk.
Founded in 2010, Redica Systems serves over 200 customers in the Pharma, BioPharma, MedTech, and Food and Cosmetics industries, including 19 of the top 20 Pharma companies and 9 of the 10 top MedTech companies. More information is available at https://redica.com/.
The Role
At Redica Systems, we are building cutting-edge solutions that help Life Sciences, MedTech, and other regulated industries manage compliance and regulatory intelligence more effectively.
We are looking for a Technical Program Manager (TPM) with 3–5 years of total experience to drive software product development initiatives across cross-functional teams.This role requires a balance of technical understanding and program management excellence to ensure the successful delivery of high-impact projects.
Key Responsibilities
About You
Must Have:
Nice to Have:
Top Pharma 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 are committed to creating a diverse and inclusive workplace where everyone feels welcomed and valued. We believe that diversity of perspectives, backgrounds, and experiences is essential to our success. We are always looking for talented individuals who can bring unique skills and perspectives to our team. All your information will be kept confidential according to EEO guidelines.

Redica Systems helps life sciences companies stay inspection ready, manage supplier risk, and keep pace with evolving global regulations. We turn the industry’s most complete regulatory and inspection data set, sourced from hundreds of health authorities and FOIA records, into trusted intelligence that quality and regulatory teams use every day to reduce compliance risk and improve oversight. Built on the Redica Catalyst Platform and Redica ID, we are evolving toward the Redica Intelligence Cloud, where internal and external data come together to provide proactive insights and guide smarter, faster decisions across the enterprise.
Founded in 2010 and with headquarters in Pleasonton, CA, Redica Systems serves over 200 customers in the pharma, biopharma, medtech, medical device, and food and cosmetics industries, including 19 of the top 20 pharma companies and 9 of the 10 top medical devices companies. More information is available at www.redica.com.