
Regulatory Intelligence Specialist
4 days ago
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.
This role is ideal for someone passionate about regulatory affairs who enjoys diving deep into data and thrives in a collaborative, fast-paced environment.
- Monitor emerging trends in the pharmaceutical and MedTech regulatory environments.
- Identify and analyze regulations, rules, and guidance document changes.
- Collaborate with teams to assess emerging trends.
- Conduct data quality checks to ensure accuracy, completeness, and integrity of regulatory data.
As a key member of our Regulatory Intelligence team, you will:
- Actively participate in global regulatory intelligence activities.
- Maintain awareness of current and relevant regulations, guidelines, policies, procedures, and practices.
- Utilize GXP expertise to identify, categorize, and analyze regulations.
- Collaborate with teams to identify emerging trends.
- Monitor and report on KPI metrics related to regulatory activities.
To succeed in this role, you should have:
- 2-4 years of experience in the pharmaceutical or medical device industries.
- A Master's degree (M.S.) in Regulatory Affairs or Quality Assurance preferred.
We offer competitive salaries, comprehensive benefits packages, and a dynamic team where you can grow and develop your skills.
Required Skills:To thrive in this role, you should possess:
- Excellent communication and decision-making skills.
- Ability to work effectively in a fast-paced environment.
- Nimble learning and adaptability.
- Tech savvy and analytical thinking.
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