Company Description
Redica Systems is a data analytics platform built to help life sciences companies improve their quality and stay on top of evolving regulations. Our proprietary 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. Redica Systems’ headquarters are in Pleasanton, CA, but we are a geographically distributed company. More information is available at www.redica.com.
Job Description
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 medical device 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, making a big impact, and helping 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 Medtech domain.
- 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.
- Partner with cross-functional teams to ensure completion of projects.
- Proactively identify opportunities to continuously improve processes, enhance data quality, and increase efficiency through automation.
About You
- Demonstrate strong organizational skills and ability to structure information.
- Ensure Quality & Excellence of Data to deliver value to the end Customer.
- Demonstrate a Continuous Improvement mindset.
- Collaborate effectively with different stakeholders and across multiple teams and departments.
- Demonstrate strong problem-solving abilities and think critically and creatively to overcome obstacles and achieve objectives.
- Possess excellent verbal and written comprehension skills.
- Efficiently manage multiple, time-sensitive projects while maintaining attention to detail and meeting deadlines.
- Show an appetite to learn and stay up to date with a highly evolving regulatory landscape.
- Display an interest in joining a forward-thinking technology company that is driving digital transformation and the delivery of quality and regulatory intelligence.
Qualifications
- 6+ years of experience in the Medtech industry with a focus on Quality Assurance, Regulatory, and/or Clinical.
- Solid Excel experience.
- Experience defining data requirements from new data sources.
- Experience framing data and providing useful output.
Additional Information
The budgeted contractor rate for this role is $40-$65 per hour. Our contractor rates are determined by role, level, and location. Within range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. People Ops can share more about specific salary ranges for your preferred location during the hiring process.
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.