Regulatory Specialist
Collins McNicholas View all jobs
- Co Westmeath
- Permanent
- Full-time
- Prepare and deliver high-quality regulatory submissions to global health authorities.
- Contribute to and support global regulatory strategies across development and commercial products.
- Author and coordinate submissions for new registrations, post-approval changes, renewals, annual reports, and line extensions.
- Coordinate and contribute to responses to regulatory agency queries and perform quality reviews of submissions.
- Maintain and track submission data, regulatory commitments, and timelines across assigned projects.
- Support the maintenance of existing global regulatory approvals.
- Communicate regulatory issues clearly to stakeholders and present solutions for resolution.
- Manage and contribute to regulatory affairs projects and cross-functional initiatives.
- Bachelor's degree (or higher) in Biology, Chemistry, Pharmacy, or a related scientific/technical discipline.
- Minimum of 3 years' hands-on Regulatory/CMC authoring experience (initial registrations and/or post-approval variations preferred).
- Experience contributing to global regulatory submissions and lifecycle management activities.
- Ability to manage multiple projects concurrently and prioritize workload effectively.
- Strong understanding of regulatory requirements and documentation standards.
- Excellent interpersonal and communication skills with the ability to work cross-functionally.
- High attention to detail, accuracy, and strong organizational skills.
- Resilient and adaptable, with the ability to perform effectively in a fast-paced, evolving environment.