Redica Systems is a technology company using data, analytics, and expertise to deliver meaningful insights to quality and safety professionals in the Life Sciences industry. By applying artificial intelligence to large and disparate government datasets, we empower the champions of quality and safety with actionable data intelligence. Our customers rely on the Redica Platform to improve compliance, drive up efficiency, and build deeper institutional memory.  

Headquartered in Pleasanton, CA we recently raised a Series B round of financing, and are rapidly writing our next chapter. We currently serve over 200 customers in the pharma, medical device, and food industries, including 19 of the top 20 pharma companies and 9 of the 10 top medical device companies.

There could be a role for you here, let's talk!

We’re looking for a curious, team-oriented, data connoisseur with a passion for getting stuff done. Your primary role is supporting and participating in proactive global monitoring and surveillance activities of the full drug development lifecycle in support of our suite of regulatory intel products and services.  

You’re the right person for the job if you’re interested in joining a high-growth company to make a big impact and help us build something amazing!

Key Responsibilities

• Play an active role in global regulatory intelligence activities, such as monitoring, acquiring, tracking, and categorizing information pertaining to the changing global regulatory landscape within the Life Science industry. 
• Participate in shaping the automation, tools, and processes supporting regulatory intelligence operations.
• Develop working knowledge of regulatory intelligence relevant to assigned projects, including structuring and analyzing large datasets. 
• Coordinate with cross-functional teams to ensure completion of assigned projects. 
• Proactively identify opportunities to continuously improve the quality of processes and increase the power of Data.

• 4+ years of experience in the Pharmaceutical industry with a focus on Quality Assurance, Regulatory, and/or Clinical.
• We are focused on hiring an individual with strong GXP experience.
• A renaissance person with a combination of strong verbal and written comprehension skills, good problem-solving abilities, and an uncanny ability to organize and structure information. 
• Solid Excel experience. 
• Proven experience effectively juggling multiple, time-sensitive projects, while maintaining crisp attention to detail.
• Interest in joining a forward-thinking technology company that is shaping the digital transformation and delivery of quality and regulatory intelligence.

Top Pharmaceutical Companies, Food Manufacturers, Medical Device Companies, and Service firms from around the globe rely on Redica Systems to gather, organize, and bring meaning to regulatory data from regulations all the way to enforcement. 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.