Regulatory Affairs Specialist
15 hours ago
We are seeking a skilled professional to support regulatory submissions and strategic projects across our diverse portfolio.
About the Role- Support regulatory submissions related to clinical trials, GMP, medicine shortages, and medical devices.
- Assist with data entry, documentation, and administrative tasks.
- Collaborate with internal stakeholders and external vendors to ensure compliance and timely delivery.
- Maintain regulatory databases and contribute to audit readiness.
- Participate in strategic projects and transversal initiatives.
Exposure to regulatory affairs, clinical trials, or GMP within the pharmaceutical or biotech industry is essential. Strong attention to detail and a focus on execution, along with excellent communication and teamwork skills, are also required.
Key Skills:
- Regulatory affairs expertise
- Clinical trial management
- Document control
- Project coordination
A fast-paced and collaborative environment with opportunities for growth and development.
How to ApplyInterested candidates should submit their applications through our online portal.
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