Manager of Regulatory Affairs - Braintree

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 ...

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. · ...

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 ...

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 ...

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 ...

We are seeking an experienced Regulatory Affairs leader to define regulatory strategy and lead IND execution for complex oncology assets. · A Boston-based, clinical-stage biotechnology company is developing next-generation precision oncology therapies. · This role is ideal for a ...

Monte Rosa Therapeutics is seeking an experienced Director of Regulatory Affairs to lead global regulatory efforts across development programs. · ...

About Us · We are a fast‑growing biopharmaceutical organization advancing a pipeline of innovative therapies aimed at transforming patient lives. As our programs progress, we are expanding our Regulatory Affairs team with a strategic, detail‑oriented leader who thrives in dynamic ...

Monte Rosa Therapeutics seeks an experienced Director of Regulatory Affairs to lead global regulatory efforts across development programs in immunology. · ...

The Manger of Regulatory Affairs is responsible for managing the regulatory and scientific aspects of projects/products including the preparation and submission of correspondence and applications to regulatory agencies. · Identifies, obtains, compiles, authors and reviews regulat ...

We believe there is a smarter, more data-driven way to make decisions in healthcare and our cloud-native AI powered SOPHiA DDM Platform makes that vision a reality on a daily basis.You will have direct input to our mission to democratize data-driven medicine for the ultimate bene ...

We are working to change the paradigm and improve the science of cancer treatment. · ...

This job involves preparing regulatory submissions while ensuring compliance with current regulations. The specialist will maintain meticulous regulatory documentation. · Proficiency in Regulatory Documentation. · Strong understanding of Regulatory Compliance. · ...

We are seeking a hands-on Director of Regulatory Affairs to lead global regulatory strategy for a Class II medical device company. This role will own 510(k) strategy, agency engagement, and submission execution in a growing, innovation-driven company. Their portfolio consists pri ...

Monte Rosa Therapeutics is seeking an experienced and strategic Director of Regulatory Affairs to lead and support global regulatory efforts across our development programs, with a focus on immunology. · ...

We are seeking an experienced Regulatory Consultant to independently lead regulatory projects and deliver high-quality, pragmatic regulatory advice to clients across the US, EU, and UK regulatory landscapes.The opportunity involves leading smaller regulatory projects end-to-end a ...

We are seeking a hands-on · Director of Regulatory Affairs · to lead global regulatory strategy for a Class II medical device company. This role will own 510(k) strategy, agency engagement, and submission execution in a growing, innovation-driven company. Their portfolio consists ...

We are seeking a Regulatory Affairs Specialist to join our Global Regulatory Affairs Team. The ideal candidate will have experience in regulatory affairs and a passion for driving innovative solutions. · ...

The Head of Regulatory Affairs will take full ownership of the end-to-end registration and filing process for innovative drugs in the U.S. market. · A Master's degree or above in Pharmacy, Biomedical Sciences, Clinical Pharmacy or related fields; · No less than 8 years of experie ...

We are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics. · 10+ years pharmaceutical/biotechnology industry experienc ...