Regulatory Liaison Manager
MSD
full-time
Posted on:
Location Type: Hybrid
Location: Brussels • Belgium
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About the role
- In this role, you will have the opportunity to coordinate regulatory activities in the EU, UK, Switzerland, and non-EU SEE countries.
- Responsible for implementing strategies for products in development with guidance and independently developing and executing strategies for registered products.
- Play a crucial role in managing submissions and interactions with the EU regulatory agencies.
- Liaise with HQ US-based cross-functional teams, effectively communicating regional requirements and ensuring compliance with all necessary regulations for assigned projects.
- Coordinate or oversee the preparation of regulatory documentation in a timely manner, aligning with corporate objectives.
Requirements
- Master's degree in pharmacy, chemistry, or equivalent, preferably in a science-related field.
- Minimum of 2 years of experience in the pharmaceutical industry is preferred.
- Strong organizational and planning skills, with the ability to manage multiple projects and adapt to changing priorities.
- Knowledge of EU regulations, guidelines, and regulatory processes for product life cycle maintenance.
- Ability to work in a cross-functional and international environment.
- Fluent written and spoken English is required, along with strong interpersonal, oral, and written communication skills.
- Willingness to travel up to 5% for job-related activities.
Benefits
- Flexible Work Arrangements: Hybrid
- Competitive salary
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
regulatory documentationregulatory strategiesproduct life cycle maintenanceEU regulationsguidelinesregulatory processes
Soft Skills
organizational skillsplanning skillsproject managementadaptabilityinterpersonal skillsoral communicationwritten communication
Certifications
Master's degree in pharmacyMaster's degree in chemistry