Regulatory Affairs Director: Average Salary in Pleasanton, CA in 2024

Director of Regulatory Affairs Body Contouring and Regulatory Innovation MPS. Directs and supports development of the regulatory strategy related to MPS activities for device regulatory activities in a variety of counties including but not limited to US, EU, US, Japan, and China. Supports regulator...

Director of Regulatory Affairs – Body Contouring and Regulatory Innovation MPS. Directs and supports development of the regulatory strategy related to MPS activities for device regulatory activities in a variety of counties including but not limited to US, EU, US, Japan, and China. Supports re...

Director of Regulatory Affairs Body Contouring and Regulatory Innovation MPS. Directs and supports development of the regulatory strategy related to MPS activities for device regulatory activities in a variety of counties including but not limited to US, EU, US, Japan, and China. Supports regulatory...

Regulatory Affairs Director required by Barrington James for an initial 12-month, remote contract opportunity with the client based in South San Francisco. ...

This Associate Director of Regulatory CMC will directly report to the Senior Director of Regulatory Affairs, CMC, and will be responsible for representing regulatory CMC on cell therapy pipeline + products. Associate Director, Regulatory Affairs CMC. Regulatory Affairs CMC experience in a pharma/bio...

They are looking to bring on a Senior Director, Regulatory Affairs to the team. Provide strategic and operational leadership in regulatory affairs, including regulatory strategies, clinical study requirements, and marketing approvals in various regions. Utilize deep knowledge of regulatory requireme...

As the Director of Regulatory Affairs, you will be a pivotal leader within the company, driving strategic regulatory decisions across the entire portfolio. Director of Regulatory Affairs. You’ll co-lead a growing regulatory team, and play a key role within regulatory submission and strategy. Regulat...

Associate Director Regulatory Affairs (Temp to Perm). Oversee regulatory submissions and approvals, ensuring alignment with global regulatory standards. Regulatory Affairs, including. Lead regulatory strategy development and execution for both U. ...

This Senior Director/Director of Regulatory Affairs will also oversee the preparation of all regulatory documents and submissions, mentor junior team members, and stay updated on changes in FDA and EU regulations. Senior Director/Director of Regulatory Affairs. Regulatory Affairs experience in a pha...

The Head of CMC Regulatory Affairs / Associate Director will lead the site Regulatory Affairs function and customer related RA CMC compliance activities. Internal regulatory support for operation and control eg:Review and approval of Lonza Regulatory Intelligence Bulletin, Interpretation of EU, US a...

As an Associate Director of Regulatory Affairs, you will represent regulatory affairs on cross-functional teams and provide regulatory advice on clinical development matters. Associate Director, Regulatory Affairs. Regulatory Affairs, regulatory submissions, drug development, oncology, FDA, EMA. Fun...

Director of Regulatory Affairs. You’d oversee regulatory filings, partner with external consultants, and eventually build out the regulatory function internally. Partner with external regulatory consultants and oversee the build-out of the internal regulatory function. This role will be pivotal in b...

Director of Regulatory Affairs, you’ll take the helm of regulatory submissions and strategic planning for successful drug approvals across key markets, including the FDA, EMA, and other regulatory agencies worldwide. Are you ready to lead regulatory strategies that bring innovative therapeutics from...

Director of Regulatory Affairs - Full Time - Onsite/Hybrid/Remote. The Director will work closely and report to the Head of Regulatory Affairs. Work closely with the Head of Regulatory Affairs to achieve company goals. Any other regulatory affairs tasks assigned or required as per the business needs...

Seeking an experienced Director of Regulatory Affairs to join a dynamic Regulatory Affairs team in a hybrid role, with some onsite presence required at our Redwood City, CA offices. Offer strategic regulatory guidance across teams (R&D, clinical, operations, legal, marketing) to align with regulator...

Responsible for reporting monthly adjustments and corrections to the Compliance Manager. ...

The specialist should be able to independently influence peers to achieve a common goal. ...

Project Manager provides guidance and support to the field service team during installation and start-up. Monitor and analyze project costs to provide recommendations for future projects. Set up and maintain project sales orders and budgets using SAP. Proficient in Microsoft Systems (Outlook, Excel,...

Assist in the preparation of regulatory submissions in support of IVDR implementation of Toxicology and Therapeutic Drug Monitoring Assays. Organize and assist in the review of materials for inclusion in regulatory submissions both in the EU and worldwide. Support the preparation of dossiers and sub...

Submits product labeling in compliance with legal/regulatory requirements and communicates planned/approved changes with operations, commercial, medical affairs and marketing. Has recognized regulatory expertise and extensive knowledge of regulatory requirements and regulations with ability to strat...

Job Title: Regulatory Affairs Associate I. Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulatory activities. Coordinate and track workflows for regulatory submissions. ...

Principal Regulatory Affairs Specialist. A leading medical device and diagnostics company is seeking a Principal Regulatory Affairs Specialist to support their growing product portfolio. Developing strategies for regulatory approval on a global scale for new and modified products. Prepare regulatory...

Administrator, Program Director, Program Manager, LCSW, LMFT, LPCC, Licensed Clinical Social Worker, Licensed Marriage and Family Therapist, Licensed Professional Clinical Counselor. ...

Job Title: Manufacturing Compliance Specialist. The specialist should be able to independently influence peers to achieve a common goal. ...

At Roche Global Regulatory Affairs, we strive to be the world's best Regulatory organization, championing patient access to the world's best diagnostics. You oversee regulatory document and submission compilation, which includes the development of submission/product registration dossiers of more com...