Life Sciences Regulatory Intelligence Specialist

2 days ago

Shimoga, Karnataka, India beBeeRegulatory Full time US$ 90,000 - US$ 1,20,000
About the Opportunity

This role presents a unique chance to contribute to the global regulatory landscape within the life sciences industry.

  • We are seeking an individual with a passion for regulatory affairs to join our team as a Data Solutions Coordinator.

The primary responsibility of this position will be to support our regulatory intelligence products and services by actively participating in global monitoring, surveillance, and data acquisition activities.

You will work closely with cross-functional teams to identify emerging trends in the pharmaceutical and MedTech regulatory environments and ensure the accuracy and integrity of our regulatory data.

This is an ideal opportunity for someone who enjoys diving deep into data and thrives in a collaborative, fast-paced environment.

Key Responsibilities:

  • Monitor and analyze the global regulatory landscape within the life sciences industry.
  • Maintain awareness of current and relevant regulations, guidelines, policies, procedures, and practices.
  • Identify, categorize, and analyze regulations, rules, and guidance document changes.
  • Collaborate with teams to identify and assess emerging trends in the pharmaceutical and medtech regulatory environments.
  • Conduct data quality checks to ensure accuracy, completeness, and integrity of regulatory data.
  • Monitor and report on key performance indicator (KPI) metrics related to regulatory activities.
  • Evaluate and recommend improvements to data acquisition and processing processes.

Requirements:

  • 2-4 years of experience in pharmaceutical or medical device industries, with focus on regulatory affairs or quality assurance.
  • A Master's degree (M.S.) in Regulatory Affairs or Quality Assurance is preferred.

Desired Skills:

  • Effective communication skills to share regulatory intelligence insights with teams and stakeholders.
  • Analytical skills to evaluate regulatory data, rules, and guidance document changes.
  • Organizational skills to prioritize multiple projects and maintain attention to detail.
  • Commitment to continuous learning and staying updated on evolving global regulatory landscape.
  • Tech savviness to leverage digital tools and technology solutions to monitor regulatory changes.

Why Join Us?

This role offers a unique opportunity to contribute to the global regulatory landscape within the life sciences industry.

We are a collaborative and fast-paced organization that values innovation and continuous improvement.

We offer competitive compensation and benefits packages, as well as opportunities for professional growth and development.

How to Apply:

Please submit your application, including your resume and cover letter, to our online portal.

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