Director, Early Precision Medicine Regulatory Affairs - Cambridge Crossing - MA - US

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. · ...

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 ...

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 ...

The Regulatory Affairs Specialist role includes obtaining and maintaining regulatory approvals, supporting quality management system objectives, and ensuring adherence to applicable regulatory standards. · Obtain and maintain regulatory approvals · SUPPORT QUALITY MANAGEMENT SYST ...

Completes a variety of administrative tasks for Regulatory project support which may include but is not limited to document formatting, document generation, document storage co-ordination and shipping of regulatory submissions. · ...

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 ...

We are seeking a Senior Regulatory Affairs Specialist to develop and implement regulatory strategies for our innovative medical imaging equipment.This individual will be responsible for preparing and managing complex submissions, ensuring compliance with evolving global regulatio ...

The Regulatory Affairs Manager will draft and file documentation and submission materials for new and/or existing products to regulatory authorities in support of global product registrations. · Cross-functional Collaboration: Collaborate with R&D PPM (product and project manager ...

The Regulatory Affairs Manager is responsible for executing regulatory strategies and ensuring compliance with global regulations. They will lead the process to obtain and maintain market approval for DeepHealth's product and product development. · Oversee the day-to-day function ...

The Regulatory Affairs Manager reports to the Director of Regulatory Affairs and is responsible for executing regulatory strategies, ensuring compliance with global regulations and leading the process to obtain and maintain market approval for DeepHealth's product and product dev ...

In this role you be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy. · ...

Beam is seeking a Manager Regulatory Affairs to progress a broad portfolio of advanced genetic medicines in a fast paced and dynamic biotech environment. · ...

+Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy.+Assist in the implementation of comprehensive regulatory strategies by ...

+Job Summary · The VP of Regulatory Affairs will lead create and drive the regulatory strategy for life cycle management activities for Vafseo Auryxia and early development programs. · ...

The Director, · Regulatory Affairs will lead global · regulatory strategy for development-stage · neuroscience programs. · <li_annual bonus opportunity medical dental vision life and AD&D short term long term disability 401(K) plan with match stock options flexible non-accrual pa ...

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

The Regulatory Affairs Specialist supports the activities of the Regulatory Affairs Department in ensuring compliance with accreditation, licensing, and regulatory requirements. · This position assists with survey readiness, documentation management, · performance tracking, · and ...

Job summary · Regulatory Affairs Manager for medical devices company. · Partner closely with the Director of Regulatory Affairs to define and implement regulatory strategies. · Provide regulatory guidance during product development to ensure compliance. · ...

We are seeking a Regulatory Affairs Specialist to support the Life Cycle Management (LCM) Regulatory Affairs team in the creation,maintenance,and review of technical documentation.This role ensures compliance with European and U.S.medical device regulations,includingsuch as EU MD ...