Associate Regulatory - Alameda

The Regulatory Affairs Associate will lead the preparation, strategy, and submission of FDA regulatory applications for medical devices.Develop end-to-end regulatory strategies that integrate clinical evidence. · Author and contribute to clinical and scientific sections of FDA su ...

The Regulatory Affairs Associate will lead the preparation and submission of FDA regulatory applications for medical devices. · ...

We are seeking a Regulatory Affairs & Quality Specialist with experience in medical devices and international regulations. · ...

Seeking a Regulatory Affairs Associate to support international addendum labelling (IFUs, import labels, and country-specific labelling) for medical devices. · ...

We are seeking a Regulatory Affairs & Quality Specialist with experience in medical devices and international regulations.This role involves handling regulatory submissions, interpreting letters from multiple countries, supporting cross-functional teams, and ensuring compliance w ...

The Senior Regulatory Affairs Specialist is responsible for managing and executing regulatory activities for Class III implantable medical devices that require governmental approval. · Prepare, author, and submit PMA supplements · ...

We are seeking a Regulatory Affairs & Quality Specialist with experience in medical devices and international regulations. · This role involves handling regulatory submissions, interpreting letters from multiple countries, supporting cross-functional teams, and ensuring complianc ...

We are looking for a Senior Regulatory Affairs Associate to join our team in Pleasanton, California. · This is an exciting opportunity to lead and innovate within the company's regulatory affairs team. The role involves ensuring compliance with federal and state regulations for p ...

The Regulatory Affairs Specialist is responsible for managing regulatory submissions and government interactions related to products requiring regulatory approval. · ...

Description · Why choose us? · Are you ready to take the next step in your career? Join us for an exciting opportunity at Albertsons Companies, where innovation and customer service go hand-in-hand · At Albertsons Companies, we are looking for someone who's not just seeking a job ...

This role is an exciting opportunity at Albertsons Companies where innovation and customer service go hand-in-hand. · Provide regulatory expertise on cross functional project teams for the Own Brands categories assigned to them. · ...

· The Regulatory Affairs Specialist is responsible for managing regulatory submissions and government interactions related to products requiring regulatory approval. · ...

Building the future of food and well-being starts with you. Join our team and bring your best self to the table. · The Own Brands Technical Services department has an opening for a Senior Regulatory Affairs Associate. · ...

The Associate Director of Regulatory Affairs will independently represent regulatory affairs on cross-functional teams and provide targeted, actionable advice across the clinical development organization. · ...

The Associate Director, Regulatory Operations will serve as a key publishing lead within the Regulatory Operations function, · responsible for managing and executing regulatory submission activities to support the company's growing pipeline and portfolio. · ...

+Job summary · The Associate Director of Regulatory Affairs will independently represent regulatory affairs on cross-functional teams and provide targeted, actionable advice across the clinical development organization. · +Demonstrate leadership within the regulatory affairs depa ...

We have an opening for a transactional/regulatory associate with 2-4 years of experience preferably with health law background or direct health care/senior care experience. · This is a fantastic chance to explore a growing and intriguing field become subject matter expert and wor ...

As a new member of the Revolution Medicines team you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. · The Associate Director Regulatory Operations will serve as a key publishing lead ...

Partnering with a high-growth clinical-stage biotech using human genetics to develop precision small-molecule medicines. · This is a hands-on Associate Director role supporting global regulatory strategy across multiple clinical programs. · ...

The Senior Associate, Regulatory Affairs reports to a Senior Director, Regulatory Affairs and will support the senior Regulatory team members. · We are seeking a highly motivated and enthusiastic individual to continue their growth in regulatory affairs by supporting the implemen ...