Manager/Associate Director, US Regulatory Affairs - Yorba Linda

The Regulatory Affairs Project Manager (RAPM) is responsible for directing and coordinating all regulatory activities associated with global Legal Manufacturer (LM) transitions across the organization. · This role oversees a defined 12-month program timeline, ensures cross-functi ...

+The Regulatory Affairs Project Manager (RAPM) is responsible for directing and coordinating all regulatory activities associated with global Legal Manufacturer (LM) transitions across the organization. · +Lead the end-to-end regulatory workstream for Legal Manufacturer changes a ...

Develop regulatory submissions and assessments to ensure timely global commercialization of products. · Ensure personal and Company compliance with all Federal State local and Company regulations policies and procedures. · ...

Career-defining. Life-changing. · iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. · ...

Develop and execute global regulatory strategies for new and existing products (e.g., dietary supplements, herbal extracts, TCM). · ...

This is a part-time Regulatory Affairs Manager position at Huisong Pharmaceuticals in Santa Ana, CA. · ...

We're looking for innovators who strive to make a difference. We care about our people and our industry of improving the health, well-being and quality of life of individuals with allergic conditions. · Lead by induvial contribution, and direct a team to prepare regulatory submis ...

We are a high-growth company with an entrepreneurial spirit that produces reliable products supported by proven clinical data. · - Familiarize with the design manufacture and clinical use of Terumo Neuro products · - Perform specific regulatory tasks for new/modifified product · ...

Be at the forefront of innovation – shape regulatory strategies that bring breakthrough therapies and life-changing technologies to patients around the world. · ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions.This role will support execution of global regulatory strategies, ensure compliance with FDA, EU, and international requirements, and collabor ...

The Post-Market Regulatory Affairs Specialist represents the Regulatory Affairs function.The position is responsible for knowledge of requirements and processes for maintaining a product in the clinical setting. · A strong candidate must have Medical Device IDE (clinical trial) e ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions. · Provide regulatory support for U.S. and global submissions. · ...

We are searching for a Director of Regulatory Affairs with deep expertise in invasive electromechanical medical devices and extensive experience preparing and submitting · 510(k) notifications. This individual will lead regulatory strategy and submissions for · devices requiring ...

We are a high-growth company looking for an intern in Regulatory Affairs to join our team. · The Regulatory Affairs team is responsible for executing regulatory strategies and obtaining approvals for our products. · This internship will provide valuable experience and skills in r ...

Become a Regulatory Affairs Advisor at Southern California Edison (SCE) and build a better tomorrow. · Lead portions of the General Rate Case (GRC) · ...

The Associate provides review and approval of marketing and sales materials for compliance; review, revision and general maintenance of regulatory files such as adverse event reporting and state registrations. · ...

The Post-Market Regulatory Affairs Specialist represents the Regulatory Affairs function and is responsible for knowledge of requirements and processes for maintaining a product in the clinical setting. · A strong candidate must have Medical Device IDE (clinical trial) experience ...

The Manager provides regulatory guidance and strategic direction for Biological and Pharmaceutical Advertising initiatives. · ...

The Regulatory Affairs Specialist will support the Director of Regulatory Affairs in regulatory compliance efforts. · Strong understanding of regulatory requirements · Effective research and analytical skills · Strong verbal and written communication skills · ...

Are you interested in working for an organization that is making a difference in people's lives every day? We're a high-growth company · ...

Job Title: · Regulatory Affairs Specialist II · Join our client's Regulatory Affairs team to support the transition to the EU's In Vitro Diagnostic Regulation (IVDR), impacting all CE-marked IVD products. · ...