Regulatory Affairs Specialist Jobs

The Regulatory Affairs Specialist at Inventprise will produce regulatory-compliant documents to support vaccine programs, manage competing priorities, and develop strategies to meet deadlines...

The Regulatory Affairs Specialist works to gain successful 510k approval by anticipating regulatory requirements, ensuring compliance, and maintaining positive relationships with regulatory bodies...

The Regulatory Affairs Specialist will assist in preparing regulatory submissions for IVDR implementation of Toxicology and Therapeutic Drug Monitoring Assays, coordinate with regulatory colleagues, m...

The Regulatory Affairs Specialist at Nordson Medical will work within the company's quality assurance system to ensure regulatory requirements are met. Responsibilities include managing document contr...

The Regulatory Affairs Specialist at Hamilton Company is responsible for analyzing new or revised regulations and standards, communicating regulatory needs to stakeholders, and managing cross-function...

The Police Sergeant position in Lake County, CA involves supervising and participating in patrol and law enforcement activities, maintaining discipline, and ensuring department rules are followed. The...

The Senior Regulatory Affairs Specialist at Abbott will lead the preparation and submission for regulatory approvals and provide guidance to cross-functional partners. The role involves acting as a re...

The Regulatory Affairs Specialist at Medtronic provides global pre- and post-market support for coronary and renal denervation medical devices, ensuring regulatory approval and compliance. This role i...

The Regulatory Affairs Specialist at Innovaderm will oversee global regulatory submissions, ensure compliance with regulations, and provide leadership for clinical trial start-ups. This role requires...

Regulatory Affairs Specialist at AgNovos responsible for preparing regulatory submissions for the company's lead product to ensure compliance with regulatory requirements in the EU, US FDA, and other...

The Regulatory Affairs Specialist ensures compliance with Canadian Medical Devices Regulations and manages regulatory applications to Health Canada. The role involves lifecycle management, product reg...

The Regulatory Affairs Specialist is responsible for implementing regulatory strategies to achieve compliance with current and upcoming regulations in the US, EU, Canada, and globally. This role invol...

The Regulatory Affairs Specialist is responsible for implementing regulatory strategies to achieve compliance with current and upcoming regulations in the US, EU, Canada, and globally. This role invol...

Werfen is seeking a Regulatory Affairs Specialist to join their team. The role involves reviewing and approving quality system documents, maintaining regulatory product files, and coordinating field a...

The Regulatory Affairs Specialist 3 at Intuitive serves as the primary regulatory representative on project and product core teams, supporting design control activities, US and Canada regulatory asses...

The Senior Regulatory Affairs Specialist will support new product development and ensure compliance with domestic and international regulatory requirements. This role involves collaborating with vario...

The Regulatory Affairs Specialist is responsible for obtaining domestic and international market access for medical and non-medical software and systems by executing regulatory strategies and collabor...

The Staff Regulatory Affairs Specialist is responsible for developing regulatory strategies for medical devices, preparing submissions to regulatory agencies, and representing the business in interact...

The Senior Regulatory Affairs Specialist will provide regulatory leadership for BD - Specimen Management, focusing on maintaining market access for existing products and supporting new product develop...

The Senior Regulatory Affairs Specialist will provide regulatory leadership for BD - Specimen Management, focusing on maintaining market access for existing products and supporting new product develop...

The Regulatory Affairs Senior Specialist coordinates regulatory activities for development projects, including new products and life cycle management. This role involves assisting with regulatory stra...

The Senior Regulatory Affairs Specialist is responsible for ensuring the marketability of Stryker's joint replacement implant devices by authoring regulatory submissions and interacting with regulator...

Seeking a Senior Regulatory Affairs Specialist to provide regulatory support in Stryker's Foot and Ankle Division, developing global regulatory strategies, supporting submissions, and interacting with...

Seeking a Senior Regulatory Affairs Specialist to provide regulatory support in Stryker's Foot and Ankle Division, developing global regulatory strategies, supporting submissions, and interacting with...

The Senior Regulatory Affairs Specialist will support the company's regulatory compliance efforts for medical devices, including software as a medical device and additively manufactured spinal implant...