regulatory affairs

milagros_palacios@rainbowagro.com Puesto: Jefe de asuntos regulatorios (Perú) Descripción del cargo Liderar la gestión de Asuntos Regulatorios en Perú, trabajando en estrecha coordinación con la Casa Matriz en China. Será responsable de definir e implementar la estrategia regulatoria local, gestionar el registro y mantenimiento de los productos de...

Puesto: Jefe de asuntos regulatorios (Perú) Descripción del cargo Liderar la gestión de Asuntos Regulatorios en Perú, trabajando en estrecha coordinación con la Casa Matriz en China. Será responsable de definir e implementar la estrategia regulatoria local, gestionar el registro y mantenimiento de los productos de protección de cultivos y asegurar...

We are seeking an experienced Medical Device Regulatory Consultant to support regulatory strategy, submissions, and compliance activities for Class II and/or Class III devices. This role will collaborate closely with cross-functional teams, ensuring products meet FDA and international regulatory requirements from development through commercialization....

Select how often (in days) to receive an alert: Create Alert Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry...

Select how often (in days) to receive an alert: Create Alert Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry...

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest...

Sylke is a fast-growing medical device company pioneering silk-based wound closure technology. Our flagship sterile dressing is FDA 510(k) exempt and rapidly expanding into international markets. With 700+ customers in our first year, Sylke is now building a pipeline of new products and investing in clinical evidence with world-class...

Job Overview Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects. Essential Functions Acts as a Regulatory Team Member on small, straightforward regulatory projects...

A medical device company in Lima is seeking a Mid-Senior level Regulatory Affairs professional. You will manage pre-510(k) readiness and ensure compliance with regulatory standards for innovative medical products. The ideal candidate has 5+ years in the field and strong knowledge of FDA and ISO regulations. The role offers a competitive salary range of...

Job Overview Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects. Essential Functions Acts as a Regulatory Team Member on small, straightforward regulatory projects...

Additional Locations:  N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the...

Job OverviewUnder general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects.Essential Functions• Acts as a Regulatory Team Member on small, straightforward regulatory projects...

A leading medical device consulting firm in Lima, Peru, is seeking a Mid-Senior level Medical Device Regulatory Consultant. The role involves developing and executing regulatory strategies, preparing submissions, and guiding compliance activities for Class II and III devices. Ideal candidates will have over 7 years of regulatory affairs experience and strong...

## Associate Director Medical Affairs IndonesiaApply: Jakarta, Indonesia: Full time: Posted Today: R By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I...

**Use Your Power for Purpose**Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, grounded in science and risk-based compliance, is both flexible and innovative, always putting the customer first. Whether your role involves development, maintenance, compliance, or...

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