- AbbVie (Pleasanton, CA)
- …Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 year ... drawings & GD&T + performing daily assigned tasks in compliance with FDA's Quality System Regulation (QSR), ISO 13485,...MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes… more
- Kelly Services (Santa Clara, CA)
- …Training Specialist** . This is a temp-hire contract with one of our Global Medical Device Robotics & Digital Solutions clients, located in **Santa Clara, CA.** ... this group you will be eligible for 50% paid Medical & Dental, a 401K plan, and a variety...to inquiries. Coordinates the performance of audits to assess compliance with quality and regulatory requirements. Demonstrates Leadership Imperatives… more
- J&J Family of Companies (Santa Clara, CA)
- …design and development. **Essential Job Functions** + Design and develop software for medical device product(s) in full compliance with the company's ... portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and… more
- AbbVie (Irvine, CA)
- …compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to… more
- AbbVie (Pleasanton, CA)
- …compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...work collaboratively with a team to design and develop medical products from initial concept through the transfer to… more
- Gilead Sciences, Inc. (La Verne, CA)
- …plans for QMS improvement + Participate in external industry committees and ensure compliance with applicable medical device and combination product ... provides comprehensive support of these combination products. **Roles/Responsibilities:** + Monitor medical device standards for quality management system (QMS)… more
- RTX Corporation (Fairfield, CA)
- …the demands of a rapidly evolving global market. As a Propellant Actuated Device (PAD) Domain Lead Engineer, this position will apply scientific principles to ... technologies, components, sub-systems, machines, tools, and systems to ensure compliance with specifications, requirements, and customer guarantees across applicable… more
- Danaher Corporation (West Sacramento, CA)
- …budget overruns. + Utilize project management tools to track progress and ensure compliance with internal policies. The essential requirements of the job include: + ... pay. We offer comprehensive package of benefits including paid time off, medical /dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay… more
- TAD PGS, Inc. (Whittier, CA)
- We have an outstanding Contract position forWarehouse Operator - Device Testing to assist our client inWhittier, CA. Pay Rate: $23.50 Job Responsibilities: Perform ... and incidents + Adherence to protocols for various operational activities + Compliance with client's assignment schedule + Ability to stand for extended periods… more
- Actalent (San Diego, CA)
- …receipt, and implementation of new and revised labeling. Required Skills: + Experience in medical device labeling and regulatory compliance + Proficiency in ... both new and existing in vitro diagnostic (IVD) and medical device (MD) products. This role requires...Clinical, and Manufacturing teams to ensure labeling accuracy and compliance . + Incorporate redlined changes into artwork drafts and… more
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