Senior Clinical Affairs Specialist, Patient Monitoring

As a Public Affairs Specialist, you will: Draft new information materials including news releases, fact sheets, brochures, booklets, broadcast spots, etc., that clarify activities and policies, and that increase communication and understanding with the organizations various publics. Perform recurring and well precedented assignments relative to the...

As a Public Affairs Specialist, you will:Draft new information materials including news releases, fact sheets, brochures, booklets, broadcast spots, etc., that clarify activities and policies, and that increase communication and understanding with the organizations various publics. Perform recurring and well precedented assignments relative to the...

Job DescriptionJob DescriptionSalary: About Carlsmed                                                                                                                             Our mission is to improve outcomes and decrease the cost of...

Job DescriptionJob DescriptionSalary: About Carlsmed                                                                                                                             Our mission is to improve outcomes and decrease the cost of...

Job DescriptionJob DescriptionSalary: About Carlsmed                                                                                                                             Our mission is to improve outcomes and decrease the cost of...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions. Essential Duties and Responsibilities * Collaborates as a core team member on new...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions. Essential Duties and Responsibilities * Collaborates as a core team member on new...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions. Essential Duties and Responsibilities * Collaborates as a core team member on new product...

Description: The Sr. Regulatory Affairs Specialist - Europe participates and manages necessary regulatory and project management activities required for medical device registration and compliance, with a focus on European Medical Device registration. The candidate must have successfully demonstrated technical proficiency, creativity, initiative, independent...

Description: The Sr. Regulatory Affairs Specialist - Europe participates and manages necessary regulatory and project management activities required for medical device registration and compliance, with a focus on European Medical Device registration. The candidate must have successfully demonstrated technical proficiency, creativity, initiative, independent...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions. Essential Duties and Responsibilities Collaborates as a core team member on new product...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions. Essential Duties and Responsibilities Collaborates as a core team member on new product...

ATEC Spine has an exciting opportunity for a Regulatory Affairs Specialist to work on-site at our location in San Diego, California. The Regulatory Affairs Specialist will support the development of submissions for domestic and international clearances for spine surgery products; as well as the support of daily activities related to product design teams,...

ATEC Spine has an exciting opportunity for a Regulatory Affairs Specialist to work on-site at our location in San Diego, California. The Regulatory Affairs Specialist will support the development of submissions for domestic and international clearances for spine surgery products; as well as the support of daily activities related to product design teams,...

Job DescriptionJob DescriptionThe Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties and Responsibilities Collaborates as a core...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties And ResponsibilitiesCollaborates as a core team member on new product...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties And ResponsibilitiesCollaborates as a core team member on new product...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties And ResponsibilitiesCollaborates as a core team member on new product...

The Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties And ResponsibilitiesCollaborates as a core team member on new product...

Description: The Sr. Regulatory Affairs Specialist - Europe participates and manages necessary regulatory and project management activities required for medical device registration and compliance, with a focus on European Medical Device registration. The candidate must have successfully demonstrated technical proficiency, creativity, initiative, independent...