
Senior Regulatory Affairs Manager
- Alajuela
- Permanente
- Tiempo completo
- Align regulatory strategies with business goals to integrate requirements into product development and improve productivity.
- Communicate clearly with teams and regulatory agencies, ensuring transparency and a proactive approach in regulatory activities.
- Drive continuous improvement through strategic partnerships and implement automation to boost efficiency.
- Evaluate the organization’s Regulatory Excellence maturity to identify areas for enhancement and guide strategic initiatives.
- Develop and update regulatory policies to ensure compliance across all business units and assess new guidelines for necessary adjustments.
- You’ve acquired 8+ years of experience with Bachelor's or 6+ years of experience with Master's in areas such as Regulatory Affairs, Quality Compliance, Product Development in the Medical Devices Industry or equivalent. You are an experienced people leader in the medical devices regulatory affairs space with extensive experience with international submissions (LATAM, Japan, China, South Korea, etc.).
- You have a bachelor's Degree/master’s degree in biomedical engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent. RAPS RAC preferred.
- Advanced English Level
- Learn more about
- Learn more about