Sr Regulatory Affairs Specialist jobs at Boston Scientific in United States, Maple Grove
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Company (1)
Job type
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Job title (1)
United States
State
Maple Grove
27 jobs found
15.08.2024
BS
Boston Scientific Sr Regulatory Affairs Specialist United States, Minnesota, Maple Grove
Act as company representative under minimal supervision, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, and submission review....
Corporate housing & relocation assistance or living stipend available for those who meet eligibility requirements. Half-day Fridays all through the summer. Free on-campus fitness center & group fitness classes. Events...
Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams. Acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written...
Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams. Acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written...
Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams. Acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written...
Reviews change notifications and performs regulatory impact assessment for product and manufacturing changes for compliance with applicable regulations and impact to regulatory filings, and supports associated global submissions as needed....
Working with Sourced Finished Medical Devices (SFMD) manufacturers for capital equipment and single-use devices from contract manufacturers and/or OEM suppliers. Utilizing strategic sourcing methodologies to lead category teams in refining...
Act as company representative under minimal supervision, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, and submission review....
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