Regulatory Affairs International Support Specialist II

at  Boston Scientific Corporation

Heredia, Provincia de Heredia, Costa Rica -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate09 Oct, 2024Not Specified10 Jul, 20242 year(s) or aboveComputer Skills,Adobe Acrobat,Oral Communication,Powerpoint,Regulatory Affairs,Biocompatibility,Microsoft Word,Excel,RegulationsNoNo
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Description:

Work mode: Hybrid
Onsite Location(s):Heredia, H, CR
Hiring Manager: Jennifer Amy Mardones Tschida
Recruiter: Jose Daniel Calderon Robles
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer and has been recognized with the Catalyst Award in 2022, a prestigious recognition of diversity, equity and inclusion excellence. Also, we have a Gender Equality Policy to support our commitment.
Hybrid Roles:
Boston Scientific’s hybrid workplace includes WFH and onsite. You will have the opportunity to discuss details in the interview.

Responsibilities:

ABOUT THIS ROLE:

With adequate supervision, the Regulatory Affairs International Support Specialist II is responsible for supporting international geographies to gain and maintain EP product approvals.

YOUR RESPONSIBILITIES WILL INCLUDE:

  • Prepare and provide appropriate documentation to international Regulatory partners for new product registrations and renewals.
  • Prepare and provide appropriate documentation to international Regulatory partners to support change submissions.
  • Support international requests for product release in collaboration with Division Regulatory product SME.
  • Liaise with international Regulatory partners for various projects as directed.
  • Support efforts to continuously improve department and divisional quality, including collaboration, best practices, and knowledge sharing.


REQUIREMENT SUMMARY

Min:2.0Max:3.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Heredia, Provincia de Heredia, Costa Rica