Associate Regulatory Affairs Jobs in USA

Responsibilities:Support and advise cross-functional teams and communicate APAC regulatory requirements and challenges effectively to meet project needs and company objectives.Oversee and direct the development of priorities timelines receipt of technical information from appropriate More...

The Associate Director Regulatory Affairs Chemistry Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients. Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory sub More...

If you have what it takes to become part of the Vistra family and would like to start a promising career with a global leader take a look at the exciting employment opportunities that are currently available and apply online.Job SummaryThe Director Regulatory Affairs is a senior leade More...

Responsibilities: The Regulatory Affairs Manager is responsible and accountable for Company Core Data Sheets (CCDS) Company Core Safety Information (CCSI) and Reference Safety Information (RSI for assigned products including regulatory responsibilities in associated change control an More...

Responsibilities: Preparing documentation for international regulatory registrations. Preparing technical documentation to compliant to MDD and EU MDR. Defining worldwide regulatory requirements are necessary for regulatory approval of products. Participating in cross functional team More...

Job Description: Individual is responsible for managing the activities for marketed product variations including authoring and compilation of chemistry manufacturing and control (CMC) sections to ensure timely preparation of submission documents. This position will coordinate activiti More...

Responsibilities: Develop and implement regulatory filing timelines for new and existing products in key markets such as US EU and Asia markets. Prepare and submit new global market device applications and amendments. Prepare and oversee the review of Traditional 510(k) Premarket Not More...

Primary Function of Position:Partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams make sure the companys regulatory affairs activities are conducted accurately ethically based upon the latest relevant reg More...

Primary Function of Position:Partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams make sure the companys regulatory affairs activities are conducted accurately ethically based upon the latest relevant reg More...

Please note that this position is can be based in San Diego CA South San Francisco CA or Princeton NJ. Acadias hybrid model requires this role to work in our office three days per week on average.Position SummaryThe Director of Regulatory Affairs (RA) Labeling will lead the developmen More...

Our Work MattersAtKindeva we make products that save lives ensuring better health and well-being for patients around the world. Our Work MattersAs a Regulatory Affairs Specialist at Kindeva your role is essential to ensuring our products remain compliant safe and accessible to patient More...

Job SummaryJob DescriptionWhat is the opportunityThis regulatory reporting role resides within the U.S. Capital Adequacy Function (Team). The Team is responsible for managing the Intermediate Holding Companys (IHCs) regulatory capital and Risk Weighted Asset (RWA) reporting under the More...

DescriptionThe Quality and Regulatory Specialist facilitates and participates in the implementation of the multidisciplinary hospital and system wide Clinical Quality and Patient Safety Performance Improvement Program. This is a healthcare professional who coordinates the planning mon More...

Nissha Medical Technologies is excited to be hiring for a Regulatory Affairs Engineer to add to our team! This positionplays a key role in ensuring compliance of medical devices to FDA EU IEC ISO and other international requirements to ensure regulatory compliance across multiple manu More...

We are the leading provider of professional services to the middle market globally our purpose is to instill confidence in a world of change empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled culture and talent experi More...

Please note that this position can be based in San Diego CA OR Princeton NJ. Acadias hybrid model requires this role to work in our office three days per week on average.Position SummaryThe Regulatory Affairs Operations Manager is responsible for publishing QC and transmittal of eCTD More...

Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe support of international product registrations and related regulatory affairs activities including execution of procedures and s More...

Responsibilities: Regulatory Labelling Documentation. Support the creation and maintenance of assigned labelling projects to enable worldwide regulatory submissions. Independently prepare and maintain the Tracking Sheets for the global regulatory dossiers related to labelling project More...

See Yourself at TelixTo support the Groups strategic objectives the Manager GRA Global will oversee Regulatory Affairs for commercial registration activities of PSMA portfolio globally. This role involves conducting regulatory tasks related to new product development securing registra More...

Job TitlePrincipal Regulatory Affairs SpecialistJob DescriptionAs a critical member of the Philips Ultrasound- Regulatory Affairs Organization the Principal Regulatory Affairs Specialist will lead and provide regulatory oversight for critical new product development projects ensuring More...