Regulatory affairs jobs in Santa Ana, CACreate job alerts

Job Description At Geiss Med Hospice, we believe in cherishing every moment of life. We understand that facing a life-limiting illness or injury can be overwhelming, which is why we are here to provide a comforting hand and a listening ear. Our team of dedicated medical professionals and compassi...

Serve as Regulatory Affairs representative on project teams to develop and implement regulatory strategies for new product commercialization with key regulatory milestone, and activities for agency filing. Minimum 7 years working registration experience in Regulatory Affairs in Medical Device, Op...

Experience: 5+ years in medical device or pharmaceutical regulatory affairs, including 5+ years of management experience and 5+ years preparing regulatory submissions (FDA, EU MDR, international). Ensures compliance with our client's Quality System and Regulatory Affairs program, reporting to the...

The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. VP of Quality & Regulatory Affairs. The Kardion Regulatory Affairs team is seeking a high energy, driven individual who is lookin...

The Regulatory Affairs Specialist will support regulatory strategies and registration activities for China and Hong Kong markets. In this role, you will manage and support product registrations and regulatory submissions specific to China and Hong Kong. Create and maintain regulatory submissions ...

Seeking an experienced regulatory leader to establish and oversee global regulatory strategy for innovative cell therapies. VP/SVP, Regulatory Affairs (FTE/permanent). Build internal regulatory capabilities and manage external partners.

Serve as Regulatory Affairs representative on project teams to develop and implement regulatory strategies for new product commercialization with key regulatory milestone, and activities for agency filing. Manager Global Regulatory Affairs shall work with a high level of autonomy to bring medical...

Vice President of Regulatory Affairs. Regulatory Affairs, with 5+ years in medical devices (Class II preferred). If you’re excited to lead regulatory strategy in a mission-driven, fast-paced environment, we’d love to connect.

Provide regulatory insights and contingency planning guidance based on local and global regulations. Collaborate with cross-functional teams (manufacturing, product development, business units) to ensure alignment with regional regulatory requirements.

The Regulatory Affairs Specialist will support regulatory strategies and registration activities for China and Hong Kong markets. Represent the regulatory function in project teams, offering guidance on China and Hong Kong regulations. In this role, you will manage and support product registratio...

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Provide regulatory insights and contingency planning guidance based on local and global regulations. Collaborate with cross-functional teams (manufacturing, product development, business units) to ensure alignment with regional regulatory requirements.

VP/SVP, Regulatory Affairs (FTE/permanent). Seeking an experienced regulatory leader to establish and oversee global regulatory strategy for innovative cell therapies. This executive role will work closely with cross-functional teams to drive development, ensure compliance, and lead regulatory in...

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Provide regulatory insights and contingency planning guidance based on local and global regulations. Collaborate with cross-functional teams (manufacturing, product development, business units) to ensure alignment with regional regulatory requirements.

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

The Regulatory Affairs Specialist will support regulatory strategies and registration activities for China and Hong Kong markets. Coordinate with in-country regulatory teams to address project status, technical documentation, and compliance requirements. Provide input on regulatory strategies and...

The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. VP of Quality & Regulatory Affairs. The Kardion Regulatory Affairs team is seeking a high energy, driven individual who is looki

Regulatory Affairs, with 5+ years in medical devices (Class II preferred). Vice President of Regulatory Affairs. Represent regulatory in board meetings and due diligence.

Serve as Regulatory Affairs representative on project teams to develop and implement regulatory strategies for new product commercialization with key regulatory milestone, and activities for agency filing. The incumbent participates on the product development team to provide regulatory guidance a...

The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. VP of Quality & Regulatory Affairs. The Kardion Regulatory Affairs team is seeking a high energy, driven individual who is lookin...

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Serve as Regulatory Affairs representative on project teams to develop and implement regulatory strategies for new product commercialization with key regulatory milestone, and activities for agency filing. Manager Global Regulatory Affairs shall work with a high level of autonomy to bring medical...

Provide regulatory insights and contingency planning guidance based on local and global regulations. Collaborate with cross-functional teams (manufacturing, product development, business units) to ensure alignment with regional regulatory requirements.

Collaborate with cross-functional teams (manufacturing, product development, business units) to ensure alignment with regional regulatory requirements. Provide regulatory insights and contingency planning guidance based on local and global regulations.

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

The Regulatory Affairs Specialist will support regulatory strategies and registration activities for China and Hong Kong markets. Coordinate with in-country regulatory teams to address project status, technical documentation, and compliance requirements. Research and review regulatory requirement...

Specialist of Regulatory Affairs you will be responsible for supporting MMS Dispensing products consisting of Medical Devices and Non-Medical Devices along with associated Software and Accessories on a global basis from a Regulatory Affairs standpoint. Knowledge of global Regulatory Affairs requi...

Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving moderately complex conflicts between those requirements and development issues; also ke...

The Regulatory Affairs Specialist is responsible for managing and maintaining regulatory approvals and clearances for assigned products in China and Hong Kong. Experience: 5-7 years of regulatory affairs experience preferred, with specific experience in China regulatory registration required. Rep...

Minimum five (5) years of experience in Regulatory Affairs. Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.

Minimum five (5) years of experience in Regulatory Affairs. Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Prepare and submit product registrations and submi...

In this high profile role, the Regulatory Affairs Specialist I will be an integral part of an expanding regulatory affairs team that is responsible for maintaining and documenting our mission critical domestic and international regulatory filings and registrations. From coordinating with internat...

Participate in representing the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving conflicts between those requirements and development issues, and/or r...

Participate in representing the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving conflicts between those requirements and development issues, and/or r...

Represents the regulatory function on project teams as a subject matter expert to provide guidance on regulatory requirements and develop worldwide regulatory strategies. Proven expertise in all aspects of Regulatory Affairs, Submission Preparation, FDA Device Law/Regulations, Worldwide Regulator...

Represent the Regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting requirements and resolving moderately complex conflicts between requirements and development issues; also keeps management ap...

From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Participate in representing the OUS regulatory function on manufacturing and product development teams to provide input on regulatory ...

Provides leadership and expertise for: regulatory strategy, regulatory operations, interactions with regulatory agencies/Notified Bodies, technical file/design dossier management and approval of Regulatory documents/statements. The Associate Director of Regulatory Affairs - Soft Tissue Fillers su...

We’re looking for Customer Support Product Testers across the US to work from home and help top brands improve their products before they hit the market.

Participate in representing the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving conflicts between those requirements and development issues, and/or r...

We’re looking for Customer Support Product Testers across the US to work from home and help top brands improve their products before they hit the market.

San Francisco, CA (Willing to travel to various Bay area job sites).Hamilton Porter has teamed up with one of the largest design-build contractors in Mid West, over 25 years of business.Seeking several Project Manager(s) to run commercial construction projects serving a variety of industries.Over...