Regulatory Affairs Specialist: Average Salary in Marlborough, MA in 2024

The Principal Regulatory Specialist is responsible for carrying out Pre-Market and Post-Market regulatory activities in compliance with Digital Factory's Quality Management System for domestic and various international markets for SaMD products. Conceive of and Implement the Regulatory Strategy in ...

Responsibilities for preparation and submission of global regulatory applications, as well as maintenance of internal regulatory file documentation. May lead small projects or represent Urology Regulatory Affairs on corporate teams, as needed. Regulatory Affairs or related experiences. Come join a g...

Principal Regulatory Affairs Specialist - Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on develo...

Principal Regulatory Affairs Specialist - Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on develo...

Principal Regulatory Affairs Specialist – Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on develo...

The Regulatory Affairs Specialist will work closely with the Director of Regulatory Affairs to obtain and maintain global regulatory approvals to allow IPG to market its state of the art devices worldwide. Senior Regulatory Affairs Specialist #24-150 | Posted 07/24/2024 Marlborough, Massachusetts Ap...

We have a robust pro Regulatory Affairs, Regulatory, Specialist, Principal, Product Development, Support, Business Services. ...

We are seeking a Regulatory Affairs Specialist to assist in the development of regulatory strategy, manage the execution of regulatory plans, and perform other activities that lead to and maintain device registrations. Represent Regulatory Affairs on cross-functional product development and manufact...

Principal Regulatory Affairs Specialist - Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on develo...

Responsibilities for preparation and submission of global regulatory applications, as well as maintenance of internal regulatory file documentation. May lead small projects or represent Urology Regulatory Affairs on corporate teams, as needed. Regulatory Affairs or related experiences. Come join a g...

We are seeking a Regulatory Affairs Specialist to assist in the development of regulatory strategy, manage the execution of regulatory plans, and perform other activities that lead to and maintain device registrations. Represent Regulatory Affairs on cross-functional product development and manufact...

This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufa...

We are seeking a Regulatory Affairs Specialist to assist in the development of regulatory strategy, manage the execution of regulatory plans, and perform other activities that lead to and maintain device registrations. Represent Regulatory Affairs on cross-functional product development and manufact...

Principal Regulatory Affairs Specialist – Endoscopy . This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Acts as a core team member on devel...

Responsible for the preparation and compiling of document packages for regulatory submissions, audits and inspections. Manage and maintain regulatory databases and technical files. Reviews materials such as labeling, marketing materials or user manuals to ensure compliance with regulatory agency req...

The Regulatory Affairs Specialist will work closely with the Director of Regulatory Affairs to obtain and maintain global regulatory approvals to allow IPG to market its state of the art devices worldwide. Regulatory affairs experience in generating applications and experience in collaboration with ...

Cherry Hill Programs brings the magic to every experience by capturing moments that last a lifetime. In partnership with retail locations, tourist attractions, and destinations across North America, Cherry Hill Programs contributes millions of holiday and souvenir experiences for children and famili...

Preclinical, Clinical, Medical Affairs, Manufacturing and Quality Control, providing regulatory guidance to aid in preparing, reviewing, and approving of regulatory NDA/IND/CTA/IMPD submissions materials. Manages a range of concurrent regulatory projects, and issues, and responds timely to ensure re...

We are seeking an experienced leader with proven management and regulatory expertise s related to. Collaborate with colleagues in Commercial, Medical Affairs, Legal, Compliance and other expertise areas in creation of promotional and disease awareness communications, field training materials, and ma...

Preclinical, Clinical, Medical Affairs, Manufacturing and Quality Control, providing regulatory guidance to aid in preparing, reviewing, and approving of regulatory NDA/IND/CTA/IMPD submissions materials. Responsible for integrating and applying knowledge of global regulations governing radiopharmac...

We are seeking an experienced leader with proven management and regulatory expertise s related to advertising/promotional materials and labeling. Collaborate with colleagues in Commercial, Medical Affairs, Legal, Compliance and other expertise areas in creation of promotional and disease awareness c...

We have an exciting opportunity for a PMO Delivery Manager, responsible for managing the development and improvement of the PMO Delivery capability within the Central Technology Portfolio Office, ensuring the effective and efficient delivery of high-quality programmes or projects. The role of PMO De...

BELFOR Project Managers have either a restoration or construction focus. Qualified candidates will be the industry expert and are local, regional, or national BELFOR resources for large projects, complex projects, and high-risk/high-profile environments. Project Managers are eligible to become BELFO...

Preclinical, Clinical, Medical Affairs, Manufacturing and Quality Control, providing regulatory guidance to aid in preparing, reviewing, and approving of regulatory NDA/IND/CTA/IMPD submissions materials. Responsible for integrating and applying knowledge of global regulations governing radiopharmac...

The Principal Compliance Specialist is responsible for providing quality support and guidance to manufacturing and support functions to ensure continued compliance to cGMP. Principal Compliance Specialist. Your job, as Principal Compliance Specialist on our Quality Assurance (QA) Operations team, wi...