Regulatory Affairs International Support Specialist II
at Boston Scientific Corporation
Heredia, Provincia de Heredia, Costa Rica -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 09 Oct, 2024 | Not Specified | 10 Jul, 2024 | 2 year(s) or above | Computer Skills,Adobe Acrobat,Oral Communication,Powerpoint,Regulatory Affairs,Biocompatibility,Microsoft Word,Excel,Regulations | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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