stents. The Opportunity We are seeking a Principal Regulatory Affairs Specialist to join Abbott’s Vascular Division... on-site in Santa Clara, CA. As an individual contributor, the Principal Regulatory Affairs Specialist is responsible...
and the market status of existing products. The Principal Regulatory Affairs Specialist will exercise a leadership role... Regulatory Affairs Specialist will assist Regulatory Affairs management by overseeing the activities required to maintain...
and develops plans for product development programs and regulatory submissions. Job Summary The Principal Regulatory Affairs... Specialist will support the Medical Solutions Regulatory affairs team. They are responsible for regulatory activities associated...
Job Title Principal Regulatory Affairs Specialist Job Description As a critical member of the Philips Ultrasound...- Regulatory Affairs Organization, the Principal Regulatory Affairs Specialist will lead and provide regulatory oversight...
Job Title Principal Regulatory Affairs Specialist Job Description The Principal Regulatory Affairs Specialist.... You're the right fit if: You’ve acquired a minimum of 7+ years’ experience in Regulatory Affairs/Strategy within FDA...
Work Flexibility: Hybrid We are seeking a Principal Regulatory Affairs Specialist to join our Medical Division.... What you will do As the Principal Regulatory Affairs Specialist, you will develop and implement environmental compliance strategies to meet...
, and accelerating access to the Enterra® Therapy. Position Summary: The Senior Principal Regulatory Affairs Specialist... years' experience in Medical Device Regulatory Affairs. Duties and Responsibilities: Responsible for the strategic...
- whatever your ambitions. About the role: We are seeking a highly skilled and experienced Principal Regulatory Affairs Specialist...: ● Serve as a regulatory affairs specialist supporting product corrections and recalls in collaboration with the Field Action...
– whatever your ambitions. About the role: We are seeking a highly skilled and experienced Principal Regulatory Affairs Specialist...: ● Serve as a regulatory affairs specialist supporting product corrections and recalls in collaboration with the Field Action...
regulatory activities required to maintain compliance to US FDA, Health Canada and EU IVD Regulations (EU) 217/46, as well... as other country regulatory agencies. Represents regulatory on design teams, prepares regulatory plans, authors US FDA 510(k)s, Health...
exemptions such as self-determined GRAS and identification data for Food Contact Notifications. Create regulatory language... and respond to FDA related technical customer inquiries. Lead cross-functional teams as needed to address regulatory compliance...
of goods sold. The role of the Senior Regulatory Affairs Specialist is focused on supporting material cost improvement projects... Senior Regulatory Affairs Specialist will develop strategies and regulatory submissions for Material Cost Improvement...
Affairs Specialist (SRA) will develop US, EU, and Canada strategies, assessments and submissions for complex projects... stakeholders. Brings Regulatory Affairs questions/issues to the attention of RA management. Comply with Teleflex's Code of Ethics...
Become part of Henry Ford Health as a full time Pharmacy Specialist - Regulatory Affairs, playing a key role... Campus This pharmacist specialist position serves as the enterprise subject-matter expert for pharmacy regulatory affairs...
Our mid-sized medical device client is adding a Principal Regulatory Affairs Specialist to the team! This Principal RA... Specialist is an expert-level team member responsible for leading regulatory activities to support global product approvals...
Description The Principal Specialist, Packaging Training & Compliance will lead the Packaging (PKG) documentation... Program. Interfaces with site management, Regulatory Affairs, production area managers and supervisors to ensure release...
- whatever your ambitions. About the role: The Corporate Clinical Quality Assurance (CQA) Principal Specialist will manage Corporate CQA..., or Regulatory Affairs Medical device industry experience required Extensive knowledge of FDA, ISO, EU MDR, and medical device...
– whatever your ambitions. About the role: The Corporate Clinical Quality Assurance (CQA) Principal Specialist will manage Corporate CQA..., or Regulatory Affairs Medical device industry experience required Extensive knowledge of FDA, ISO, EU MDR, and medical device...
towards an exciting future. The Principal Compliance Specialist, Product Stewardship will ensure Edwards devices meet the material... Stewardship Group, with a growing focus on sustainability and environmental initiatives. The Principal Compliance Specialist...
: . Job Description As a Senior Principal Medical Safety Specialist (Sr.Pr. MSS) you will have an integral role in the day-to-day functioning of the... across Medical & Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs, Research...