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Regulatory Intelligence Associate

Company Description

Redica Systems is a forward-thinking technology company using 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 devices companies. 

We’re headquartered in Pleasanton, CA, and are open to remote work for candidates residing in the US. Let's talk! 

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 drug development lifecycle in support of our suite of regulatory and compliance intel products and services. 

You’re the right person for the job if you’re looking to get in on the ground floor of a company experiencing high growth and are looking to make a big impact and help build something amazing with us!

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 quality compliance and regulatory intelligence relevant to assigned projects, including structuring and analyzing compliance data. 
  • Capable of analyzing large datasets relevant to quality and compliance.
  • Coordinate with cross-functional teams to ensure completion of assigned projects. 

  • 1 - 3 years of experience in the Pharmaceutical or Medical Device industries with a focus on Quality Assurance, Regulatory, or Compliance.
  • A renaissance person with the combination of 
    • Strong verbal and written comprehension skills. 
    • Good problem-solving abilities. 
    • Strong math and organizational skills.
  • Solid Excel experience 
  • A desire to learn, be coached, improve performance, and take on additional responsibilities. 
  • Proven experience effectively juggling multiple, time-sensitive projects, while maintaining crisp attention to detail.
  • A keen interest in joining a forward-thinking technology company that is shaping the digital transformation and delivery of quality and regulatory intelligence.

Additional Information

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.

Before you apply, please check if any restrictions apply in terms of time zone or country.

This job has a geo-restriction in place:  USA Only.

REDICA Systems

This job listing is archived
Category Business
Job type Full-time
Hiring from USA Only
Date Posted 1yr ago

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