Associate Director, Regulatory Affairs - Norwood, MA

As a pivotal member of the Corbus Product Development Team(s) (PDT) supports Corbus' drug development by leading the preparation and/or oversight of regulatory submissions and inputting into the regulatory strategy as the US regulatory lead for Corbus' programs. · This role will ...

· As a pivotal member of the Corbus Product Development Team(s) (PDT) supports Corbus' drug development by leading the preparation and/or oversight of regulatory submissions and inputting into the regulatory strategy as the US regulatory lead for Corbus' programs.  · This role w ...

This is a Regulatory Affairs & Compliance Lead role at Sensitech, where you will be the regulatory subject-matter expert for their comprehensive product portfolio. · Develop and implement regulatory strategies for new and modified products to enable entry into target markets. · ...

Sensitech Inc., a Carrier company under the Climate Solutions Transportation (CST) segment, is a global leader in supply chain visibility solutions. Sensitech helps ensure the quality and integrity of temperature-sensitive products across the pharmaceutical, food, and industrial ...

As the Regulatory Affairs & Compliance Lead at Sensitech, you will be the regulatory subject-matter expert for our comprehensive product portfolio. · The Regulatory Affairs & Compliance Lead collaborates cross-functionally with Product Development, Quality, Manufacturing, Marketi ...

We are seeking a Regulatory Affairs & Compliance Lead to join our team at Sensitech Inc., a global leader in supply chain visibility solutions. As the regulatory subject-matter expert for our comprehensive product portfolio, you will collaborate cross-functionally with Product De ...

The Regulatory Affairs Associate role at SharkNinja involves managing customer complaints within the organization's Quality Management System (QMS). This includes reviewing submissions for completeness, logging complaints accurately in the QMS, and ensuring timely progression thr ...

The Regulatory Affairs Specialist is responsible for coordinating customer complaints within the organization's Quality Management System (QMS). This role ensures accurate recording and processing of complaints in compliance with internal procedures, ISO 13485, and applicable reg ...

The Regulatory Affairs Specialist is responsible for coordinating customer complaints and ensuring compliance with internal procedures and regulatory requirements. · Monitor designated sources for new complaints. · Accurately log complaints in the QMS. · ...

As a Regulatory Affairs Specialist at Mass General Brigham, you will be responsible for ensuring compliance with regulatory requirements and maintaining an updated library of FDA regulations and guidance documents. · AUTHORS AND REVIEWS OF STANDARD OPERATING PROCEDURES,T techNICA ...

Job summary: Join a company where you will have an opportunity to grow professionally and personally and give strength to others by Empowering Healing. We offer a strong benefits package opportunities for growth and the chance to contribute to our mission: · to provide an integr ...

We are seeking a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for clinical trials and deliver consulting services to ensure that the company meets regulatory requirements. · ...

We are currently looking for an ambitious Principal Regulatory Affairs Specialist to join our Endovascular Robotics business within Advanced Therapies. · We believe the combination of endovascular robotics, image guidance, and dedicated devices will change the way neurovascular p ...

We all share the same goal - to improve the world's health. · ...

We have unique opportunities and are always looking for exceptional talent. Join a company where you will have an opportunity to grow professionally and personally and give strength to others by Empowering Healing. · ...

Parexel International LLC seeks a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for clinical trials. The position may telecommute from anywhere in the United States up to 5 days per week. · ...

Competitive Power Ventures, Inc. ("CPV"), with headquarters in Silver Spring, MD, and an office in Braintree, MA is a leading clean energy company built around the belief that progressive companies can be powerful leaders in creating a better world. · CPV is looking for a Manager ...

We are seeking a Vice President, Regulatory Affairs (Advertising, Promotion, and Labeling) to join our team. · The role provides strategic leadership across Marketing, Medical Affairs, Legal, Clinical, and Commercial teams, · guiding risk-based decisions and enabling compliant bu ...

We are seeking a Director, Regulatory , CMC to join our team. · This position reports to the Executive Director, Regulatory Affairs , CMC and will be based out of Boston . MA USA in our Needham office Hybrid positions require a minimum of two onsite days per week On-site position ...

We are looking for a talented and detail-oriented Regulatory Affairs Specialist with 2-3 years of experience in regulatory affairs, · specifically with expertise in regulatory codes, particularly USDA codes.Ensure compliance with regulatory standards and codes governing the food ...