ZOLL Medical Corporation
Regulatory Affairs Program Lead
ZOLL Medical Corporation, Charleston, West Virginia, us, 25329
ZOLL Medical Corporation
Regulatory Affairs Program Lead
Charleston ,
West Virginia
Apply Now
At ZOLL, we're passionate about improving patient outcomes and helping save lives.We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions.The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service.At ZOLL, you won't just have a job. You'll have a career-and a purpose.Join our team. It's a great time to be a part of ZOLL!Job SummaryThe Regulatory Affairs Program Lead is responsible for managing the collaboration with cross-functional stakeholders to ensure regulatory compliance is met. The Regulatory Affairs Program Lead will oversee the technical liaison(s) between cross-functional departments and the Regulatory Affairs team.Essential FunctionsAbility to evaluate and resolve regulatory and technical issues due to extensive knowledge of medical device manufacturing and related regulatory requirements in this product sector through a clear understanding of the product development lifecycleLead technical medical device compliance initiatives, including assessing and communicating technical guidelines to support pre-market requirementsDrive education of regulatory compliance to key business stakeholdersLead a team of product technical subject matter experts who support the Regulatory Regions teams to meet the requirements of regulatory bodies.Review global regulatory submissions for technical accuracy and regulatory compliance.Support technical inquiries for the medical device regulatory submissions, registrations, licenses, clearances, approvals, and deficiencies for global market entry.Initiate reviews of change requests and regulatory strategies for new product innovations or devices changes. Works collaboratively with the Regulatory Regions team to assess regulatory impact.Ability to lead a team to collaborate with Engineering and R&D to develop the standards strategy for medical devices and supports activities required to maintain regulatory compliance as new or revised versions of standards are released.Ability to lead a team to collaborate with R&D and Quality Assurance in the development of risk management plans and hazard analysis for ZOLL products.Ability to lead a team to collaborate with key stakeholders to ensure and improve efficiencies throughout design documentation in accordance with regulatory requirements and best practicesCommunicates clearly and effectively with cross-department personnelParticipate in regulatory audits/inspections as requiredAuthor and maintain standard operating procedures (SOPs) and train key personnel as neededRequired/Preferred Education and ExperienceBachelor's Degree required7+ years of regulatory experience in the Medical Device IndustryPrevious experience working with Regulatory Authorities relative to premarket and compliance activities.Knowledge, Skills and AbilitiesStrong Project management skillsMust be able to work under pressure to meet regulatory reporting time frames and company requirementsMust be able to work with minimal supervision, recognize departmental needs and initiate/recommend actions for resolutionExperience interacting with FDA and/or other regulatory agenciesMust work well in team environmentsMust demonstrate leadership skills in team settingProven analytical abilities, able to apply problem-solving skills for problems of moderate to diverse... For full info follow application link.
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Regulatory Affairs Program Lead
Charleston ,
West Virginia
Apply Now
At ZOLL, we're passionate about improving patient outcomes and helping save lives.We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions.The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service.At ZOLL, you won't just have a job. You'll have a career-and a purpose.Join our team. It's a great time to be a part of ZOLL!Job SummaryThe Regulatory Affairs Program Lead is responsible for managing the collaboration with cross-functional stakeholders to ensure regulatory compliance is met. The Regulatory Affairs Program Lead will oversee the technical liaison(s) between cross-functional departments and the Regulatory Affairs team.Essential FunctionsAbility to evaluate and resolve regulatory and technical issues due to extensive knowledge of medical device manufacturing and related regulatory requirements in this product sector through a clear understanding of the product development lifecycleLead technical medical device compliance initiatives, including assessing and communicating technical guidelines to support pre-market requirementsDrive education of regulatory compliance to key business stakeholdersLead a team of product technical subject matter experts who support the Regulatory Regions teams to meet the requirements of regulatory bodies.Review global regulatory submissions for technical accuracy and regulatory compliance.Support technical inquiries for the medical device regulatory submissions, registrations, licenses, clearances, approvals, and deficiencies for global market entry.Initiate reviews of change requests and regulatory strategies for new product innovations or devices changes. Works collaboratively with the Regulatory Regions team to assess regulatory impact.Ability to lead a team to collaborate with Engineering and R&D to develop the standards strategy for medical devices and supports activities required to maintain regulatory compliance as new or revised versions of standards are released.Ability to lead a team to collaborate with R&D and Quality Assurance in the development of risk management plans and hazard analysis for ZOLL products.Ability to lead a team to collaborate with key stakeholders to ensure and improve efficiencies throughout design documentation in accordance with regulatory requirements and best practicesCommunicates clearly and effectively with cross-department personnelParticipate in regulatory audits/inspections as requiredAuthor and maintain standard operating procedures (SOPs) and train key personnel as neededRequired/Preferred Education and ExperienceBachelor's Degree required7+ years of regulatory experience in the Medical Device IndustryPrevious experience working with Regulatory Authorities relative to premarket and compliance activities.Knowledge, Skills and AbilitiesStrong Project management skillsMust be able to work under pressure to meet regulatory reporting time frames and company requirementsMust be able to work with minimal supervision, recognize departmental needs and initiate/recommend actions for resolutionExperience interacting with FDA and/or other regulatory agenciesMust work well in team environmentsMust demonstrate leadership skills in team settingProven analytical abilities, able to apply problem-solving skills for problems of moderate to diverse... For full info follow application link.
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