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Job alert Jobs 11 - 20 of 424

Med-Tech Media Marketing Specialist

Zeto, Inc  –  Santa Clara, CA
... Devise media mrktng strategies for FDA-cleared med devices for media & public - Jun 11

IVD Signal Analysis Engineer

Yoh, A Day & Zimmermann Company  –  San Jose, CA
... The position requires knowledge of FDA regulatory processes for IVD products. Pay Rate: $90.00 to $110.00/Hr. Type: on-site position. Job Description: We are seeking a highly skilled Automation and Verification Engineer to join our dynamic team, ... - Jun 18

Machine Operator

Avanti MFG  –  Milpitas, CA, 95035
... Distinguish between an FDA Product and non-FDA product and follow proper FDA rules and protocols when applicable. Collect standard samples and for QA testing. Add re-feed to the machines as needed. Perform manual/automatic operations of the Rewinder ... - May 23

Analytical Data Scientist

F. Hoffmann-La Roche AG  –  San Jose, CA
... Data collection and database in clinical trials following industry and FDA data standards; Food and Drug Administration (FDA) and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines ... - Jun 08

Regulatory Affairs Project Manager

GForce Life Sciences  –  Santa Clara, CA, 95053
... Skills: Knowledge of US and/or Canadian regulations relating to product and/or device clearance (FDA). Effective verbal and written communication skills, negotiation skills, and conflict management skills. Ability to work constructively with ... - Jun 18

Director of Software

Visby Medical  –  San Jose, CA
... Ensure the team adheres to coding standards, conducts thorough testing, and follows rigorous deployment processes to ensure high functioning and well documented software that can be included in an FDA submission prior to being cleared for use in ... - Jun 12

Sr Quality Assurance Engineer

Cordis  –  Santa Clara, CA
... Provide regulatory support and assist with various ongoing projects to remain in compliance with all FDA and other U.S. and international regulatory requirements. Please note, at this time Cordis is not sponsoring applicants for any type of work ... - May 29

Sr. Clinical Data Engineer (Non-IT)

Yoh, A Day & Zimmermann Company  –  San Jose, CA
... At least 5 years of experience in the medical device IVD industry, with a strong understanding of FDA regulatory standards and compliance requirements. Expert proficiency in Python programming and software engineering principles. Adept at queries, ... - Jun 20

Senior Quality Specialist

Kelly Science, Engineering, Technology & Telecom  –  Sunnyvale, CA, 94087
... Quality Specialist is responsible for supporting quality systems activities related to assay development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product ... - Jun 18

Quality Engineer - Hybrid

Cannon Quality Group  –  San Jose, CA
... suppliers and vendors EXPERIENCE REQUIREMENTS: 2+ years of in-depth Quality System implementation in compliance with FDB, FDA, and ISO 13485 2+ years of multiple simultaneous project QA or client facing QA consultancy Experience should include ... - May 31
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