Associate Director, Regulatory Affairs - Framingham, MA

The Associate Director Regulatory Affairs will join the Regulatory Development team at KalVista in contributing to the development of regulatory submissions in alignment with company objectives and support the successful commercialization of KalVista's products. · The position pr ...

The Associate Director Regulatory Affairs will join the Regulatory Development team at KalVista in contributing to the development of regulatory submissions in alignment with company objectives and support the successful commercialization of KalVistass products. · ...

The Associate Director Regulatory Affairs will join the Regulatory Development team at KalVista in contributing to the development of regulatory submissions in alignment with company objectives and support the successful commercialization of KalVista's products. · Servirá como lí ...

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 Manager to join our team in Regulatory Affairs. The successful candidate will be responsible for managing regulatory submissions, providing technical guidance to the team, and developing short-range regulatory strategies. · Direct and coordinate activities of Reg ...

· Additional Location(s): US-MA-Marlborough · Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance · At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing emp ...

Job summary · Boston Scientific is seeking a Regulatory Affairs Manager to support the Urology business unit. The successful candidate will be responsible for supporting existing product lines, developing new technologies, and managing CAPAs. · ResponsibilitiesDirect and coordina ...

The Regulatory Affairs Leader - Pharma may be involved in Pre or Postmarket duties or both. · File / Maintain regulatory deliverables. · Analyze & communicate changes and proposed changes to country regulations through Regulatory Intelligence and implement strategies. · ...

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 ...

This role involves providing regulatory expertise on multiple products, technologies, and regions. · As a Regulatory Subject Matter Expert (SME), you will devote significant time to leadership at both the franchise level and functional level, · including department employee devel ...

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 ...

· Company Description · Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, ...

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. · ...

The Director, Regulatory Affairs will be responsible for the strategic leadership, · development and execution of science-based, solution-oriented, · and globally aligned regulatory strategies for the program(s) · under his/her accountability.This role serves as a key · regulator ...

The Regulatory Support Manager will provide support to Product Managers Regions and Customers by providing quality documents and regulatory support in response to customers requests for quality regulatory and technical-related information. · ...

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

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. · ...

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 ...

Nazwa biura: USA - Maryland - Rockville, Durham Blackwell Street, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence · Posted Date: Feb · Business Introduction · At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion ...