Global Regulatory Compliance Expert

24 hours ago

Thiruvananthapuram, Kerala, India beBeeAnalysis Full time ₹ 8,00,000 - ₹ 15,00,000
Regulatory Intelligence Specialist

About the Company

We are a leading data analytics company serving the life sciences sector. Our global team empowers companies to enhance product quality and stay ahead of evolving regulations.

We leverage one of the industry's most comprehensive datasets, sourced from hundreds of health agencies and government records. Our customers use our platform to more effectively manage their inspection preparation, monitor supplier quality, and perform regulatory surveillance.

About the Role

You will play a critical role in monitoring and analyzing the global regulatory landscape within the life sciences industry. Your primary responsibility 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 role is ideal for someone passionate about regulatory affairs who enjoys diving deep into data and thrives in a collaborative environment.

Key Responsibilities:
  • Actively participate in global regulatory intelligence activities, including monitoring, acquiring, tracking, and categorizing information related to the evolving global regulatory landscape within the life sciences industry.
  • Maintain a thorough awareness of all current and relevant regulations, guidelines, policies, procedures, and practices.
  • Utilize a strong understanding of GXP to proactively 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 the accuracy, completeness, and integrity of regulatory data.
  • Monitor and report on key performance indicator (KPI) metrics related to regulatory activities.
  • Ensure that all data acquisition and processing processes are clearly defined and consistently followed, while also recommending and implementing improvements where necessary.
Requirements

To succeed in this role, you should have:

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

We offer competitive salaries, comprehensive benefits packages, and a dynamic team where you can grow and develop your skills.

We believe in creating a diverse and inclusive workplace where everyone feels welcomed and valued. We are committed to diversity of perspectives, backgrounds, and experiences as essential to our success.

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