Regulatory Affairs Jobs in USA

Innovation starts from the heart. At Edwards we put patients first. We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structural heart disease. Aortic stenosis impacts millions of people globally yet it ofte...

Job Category:Legal Compliance & AuditJob Family:Compliance & Regulatory AffairsJob Description:As a Regulatory Compliance Manager you will provide global leadership strategic ideas and apply Operations regulatory guidance to develop processes that ensure executional excellence in Regulatory programs...

DescriptionSchool Information:Located in Roseville MI Reach Academy opened in 2008 and serves students K-8. At Reach you can connect passion with purpose.To learn more about Reach Academy click here.Why Choose Reach Academy:Starting pay above market scales.Competitive benefits at affordable rates.Ac...

DescriptionSummary:We are currently seeking dedicated Speech Language Pathologists (SLPs) to join our team in a virtual hybrid or in-person role. As a virtual hybrid or in-person SLP youll have the opportunity to make a meaningful impact while helping students reach their full potential.This positio...

DescriptionThis role is eligible for a signing bonus up to $5000.Summary:We are currently seeking dedicated Speech Language Pathologists (SLPs) to join our team in a virtual hybrid or in-person role. As a virtual hybrid or in-person SLP youll have the opportunity to make a meaningful impact while he...

Hims & Hers is the leading health and wellness platform on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable accessible and personal from diagnosis to treatment to del...

Purpose:The Analytical Stability Chemist is responsible for the coordination and organization of stability studies to ensure uninterrupted daily operations associated with procurement dispensing studying analyzing and reporting of those studies while assuring compliance for Stability and Laboratory...

The Senior Director Regulatory Portfolio Management is accountable for providing program and project management support across the Regulatory Affairs (RA) organization. This includes project management in support of all Global Regulatory Product Teams (GRPTs) as well as the management of the portfol...

Responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development.This individual demonstrates the ability to combine knowledge of scientific regulatory & business issues to enable de...

Primary Function of the Position  As part of the Intuitive Human Factors team the Senior Human Factors Engineer works closely with designers clinical engineers system and software engineers technical product managers regulatory affairs and other important functional teams. The Senior Human Factors E...

PURPOSE:The Medical Science Liaison (MSL) Director role is responsible for providing leadership strategic direction and day-to-day direct line management of a MSL team. They are accountable to ensure the team is adequately staffed (according to local needs) trained (therapeutic and functional) and c...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to commercially di...

DescriptionSummary:We are currently seeking dedicated Speech Language Pathologists (SLPs) to join our team in a virtual hybrid or in-person role. As a virtual hybrid or in-person SLP youll have the opportunity to make a meaningful impact while helping students reach their full potential.This positio...

Bring more to life.Are you ready to accelerate your potential and make a real difference within life sciences diagnostics and biotechnologyAt Beckman Coulter Life Sciences one of Danahers 15 operating companies our work saves livesand were all united by a shared commitment to innovate for tangible i...

Job DescriptionIn June 2019 Vertex announced the establishment of new research sites in Boston and Providence where research development and clinical manufacturing for cell biologic and genetic therapies will be primarily based. Cell and genetic therapies represent two rapidly emerging therapeutic m...

Position Details: Our client a world-leading Pharmaceutical Company in San Diego CA is currently looking for an Quality & Regulatory Affairs Lead to join their expanding team. Job Title: Quality & Regulatory Affairs Lead / Pharma Manufacturing / Hybrid Work Duration: 15 months contract extendable...

Job Title: Clinical Scientist Medical DevicesLocation: Newark DELong Term ContractRole:Clinical Scientist responsible for developing Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER) to support CE Mark regulatory submissions for medical devices.Key Responsibilities:Develop and a...

The Senior Manager Quality (IQA/SQA) provides leadership and direction to the Quality Function they are responsible for within Operations. This Sr. Manager role is responsible for the effective implementation of AbbVie Quality Systems for which they are responsible for. This could include: Incoming...

The Associate Director Clinical QA is responsible for developing and implementing a strategy for proactive quality oversight of clinical development programs within their responsibility.This role will ensure that R&D remains in compliance with the corporate policies and applicable worldwide regulati...

The Associate Director Clinical QA is responsible for developing and implementing a strategy for proactive quality oversight of clinical development programs within their responsibility.This role will ensure that R&D remains in compliance with the corporate policies and applicable worldwide regulati...