Chairman of the Board of Management, Chief Executive Officer

Group CFO

New film from Covestro unlocks medical device capabilities

Covestro delivers new solution for in-home electronic stethoscope

Rondo Energy, Covestro break ground on 100MWh thermal energy storage site in Germany

Dr. Sultan Al Jaber made Honorary Fellow of the Energy Institute for leadership in energy, AI and economic growth

FDA Regulatory Affairs Principal Specialist

Covestro is a company that refines chemical material solutions with innovative products. They are seeking an FDA Regulatory Affairs Principal Specialist to ensure compliance with North American federal regulations for food packaging, focusing on the Food, Drug, and Cosmetic Act.

Chief Operating Officer, Transfusion & Transplant

Human Resources Business Partner

Volition Issues Business Review 2025

WERFEN APPLAUDS SIGNIFICANT PUBLICATION URGING ACTION ON THE RISKS OF UNDETECTED HEMOLYSIS

In Vitro Diagnostics Market Report Unveils Key Commercial Prospects

VolitionRx Limited Announces Third Quarter 2025 Financial Results and Business Update

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Senior Principal Regulatory Affairs Specialist

Werfen is a growing, family-owned, innovative company specializing in diagnostics. The Senior Principal Regulatory Affairs Specialist is responsible for managing pre-market regulatory activities to ensure compliance with US FDA, Health Canada, and EU IVD Regulations, while also preparing regulatory submissions and conducting labeling reviews.

Chief Operating Officer

Understanding The Growth Of The Prenatal Genetic Testing Industry By 2035

Global Blood Coagulation Analyzers Market to Surpass USD...

Detecting and monitoring oral anticoagulants or intravenous direct thrombin …

Optical analyte sensor

Werfen North America is a family-owned, innovative company that specializes in diagnostics. They are seeking a Senior Principal Regulatory Affairs Specialist to manage pre-market regulatory activities and ensure compliance with US FDA, Health Canada, and EU IVD regulations, while also representing regulatory interests on design teams.

Chief Business Officer

Enlil Launches Integrations with Bill.com, Onshape, and SolidWorks

Laza Medical Achieves First-in-Human Use of Real-Time AI Heart Model for Ultrasound-Guided Cardiac Procedures

Myra Vision Secures FDA Approval to Initiate US IDE Study in Glaucoma

ADONA MEDICAL COMPLETES ENROLLMENT IN FIRST-IN-HUMAN TRIAL FOR NOVEL INTERATRIAL SHUNT FOR PATIENTS WITH HEART FAILURE

Principal Regulatory Affairs Specialist

Shifamed is a medical device innovation hub focused on developing novel medical products. The Principal Regulatory Affairs Specialist will manage regulatory affairs activities for a class III mechanical circulatory support system, including submission strategy and preparation for US, EU, and Japan.

President & Chief Executive Officer

Senior Vice President

Abbott Reports Fourth-Quarter and Full-Year 2025 Results; Issues 2026 Financial Outlook

Abbott receives CE Mark for the TactiFlex™ Duo Ablation Catheter to treat patients with abnormal heart rhythms

Medtronic Diabetes announces FDA clearance for MiniMed Go™ Smart MDI system featuring Instinct sensor made by Abbott

Abbott's FreeStyle Libre 3 Plus Now Covered Across Canada Français

Abbott is a global healthcare leader that helps people live more fully at all stages of life. The Principal Regulatory Affairs Specialist position is responsible for leading strategic planning and developing innovative solutions to ensure timely regulatory registration and release of products for distribution in the Asia Pacific market.

Principal Regulatory Affairs Specialist – APAC - Diabetes Care (on-site)

Chief Financial Officer

Women exec moves at Unilever, Rothy’s, and more to watch this week

Insulet to Participate in 44th Annual J.P. Morgan Healthcare Conference

Insulet Corporation Announces FDA 510(k) Clearance of Omnipod® 5 Algorithm Enhancements That Redefine Insulin Delivery and Simplify the Pod Experience

Insulet gets FDA clearance for updates to Omnipod 5 Automated Insulin Delivery

Insulet Corporation is an innovative medical device company dedicated to simplifying life for people with diabetes through its Omnipod product platform. The Principal Regulatory Affairs Specialist will lead strategic regulatory initiatives and projects, ensuring regulatory approval and compliance of medical devices in both domestic and international markets.

Principal Regulatory Affairs Specialist (Hybrid)

Chief Executive Officer

Study Begins for Enterra Medical’s Chronic Nausea Treatment Device

Enterra Medical Introduces the new, FDA approved Enterra ReliaStim® as the Next Step Toward the Future of GES Therapy

New Hope for Chronic Nausea: Enterra Medical Begins NAVIGATE Study After Gaining FDA IDE Approval and Breakthrough Device Designation

Methods, Systems, Devices And Components for Miniaturized Implantable Gastric …

Enterra Medical is a medical device company dedicated to a singular focus: helping more people with chronic gastroparesis live better lives by advancing technology, expanding clinical science, and accelerating access to the Enterra® Therapy. The Senior Principal Regulatory Affairs Specialist will be responsible for regulatory strategies and associated daily activities, ensuring compliance with FDA and international standards.

Chairman, President & CEO

If You Invested $1000 In Boston Scientific Stock 5 Years Ago, You Would Have This Much Today

Expert Outlook: Boston Scientific Through The Eyes Of 6 Analysts

Boston Scientific earnings on deck after Q3 miss, Penumbra deal

Boston Scientific ratings affirmed by Fitch, outlook positive

Boston Scientific is a leader in medical science, and they are seeking a highly skilled and experienced Principal Regulatory Affairs Specialist to join their Interventional Cardiology and Vascular Therapies Division. In this pivotal role, you will ensure global regulatory compliance across various post-market surveillance domains and collaborate with cross-functional teams to drive compliance and continuous improvement.

Executive Chair of the Board of Directors (previously CEO)

President and CEO

EBR Systems to Participate at the Canaccord Genuity MedTech, Diagnostics and Digital Health & Services Forum

EBR Systems Achieves First Enrollments in the WiSE-UP Study for Heart Failure Patients

EBR Secures NTAP and TPT Reimbursement for the WiSE System, effective October 1, 2025

Wireless Pacemaker Leads Market to Reach USD 561 Mn by 2035, Driven by Leadless Innovation & Rising Cardiac Care Demand

EBR Systems, Inc. is a pioneering company in cardiac technology, known for developing the world’s first FDA approved, leadless left ventricular endocardial pacing device for heart failure. The Principal Regulatory Affairs Specialist will lead regulatory projects, ensure compliance with medical device regulations, and mentor team members while driving regulatory strategies to support business objectives.

Boston Scientific is a leader in medical science, committed to solving important health industry challenges. The Principal Regulatory Specialist will be responsible for planning, authoring, managing, and implementing regulatory submissions to various global regulatory agencies, ensuring compliance and supporting worldwide product approvals.

Chair & CEO

Chief Financial Officer and Vice President

Neurointerventional Devices Market is Projected to Increase at a CAGR of 7.2% Through 2025-2029

UAE General Surgery Devices Market Trends & Opportunities, 2020-2024 & 2025-2030 | Minimally Invasive Surgical Technologies Gain Traction, Advanced General Surgery Devices Fuels Demand

Stryker announces Allan Golston will retire from Board of Directors

Stryker announces the retirement of Glenn S. Boehnlein and the promotion of Preston Wells to Vice President, Chief Financial Officer

Stryker is seeking a Principal Regulatory Affairs Specialist to join their Medical Division. This role involves developing and implementing environmental compliance strategies to meet various regulations, influencing design and manufacturing processes, and managing compliance issues for new product development and sustaining projects.

Non Executive Director

Consultant for distributors of medical devices

Urodynamic Equipment and Consumables Market Size to Hit Nearly USD 808.16 Million by 2034

Laborie to acquire Organon’s JADA System for $465M

Laborie Announces Agreement to Acquire the JADA® System from Organon

Organon to Sell Jada System to Laborie Medical Technologies

Laborie is a world-class specialist medical company focused on advancing technologies that preserve and restore human dignity. The Principal Regulatory Affairs Specialist is responsible for leading regulatory activities for global product approvals and lifecycle management, ensuring compliance with global regulations and corporate standards.

Stryker is a leading medical technology company, and they are seeking a Principal Regulatory Affairs Specialist to join their Medical Division. This role involves developing and implementing environmental compliance strategies to meet various regulations and influencing design and manufacturing processes for new product development and sustaining projects.

Influential Women Profiles Julie Wilhelmson: Leader in Quality and Regulatory Excellence in the Medical Device Industry

Bracco Medical Technologies is seeking a Principal Regulatory Affairs Specialist responsible for developing and implementing regulatory strategies across various projects and products. The role involves collaborating with internal stakeholders and external consultants to ensure compliance with regulations and maintain product approvals.

Fda Regulatory Affairs Principal Specialist

Fda Regulatory Affairs Principal Specialist in united states (1000+)

FDA Regulatory Affairs Principal Specialist

Senior Principal Regulatory Affairs Specialist

Senior Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist – APAC - Diabetes Care (on-site)

Principal Regulatory Affairs Specialist (Hybrid)

Senior Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist