- US Tech Solutions (San Francisco, CA)
- …in program/project management for Software development. + 2+ years working with quality assurance, device testing, or customer technical support triaging. + ... management work to ensure we deliver, with velocity, high quality features to our users. + This project/position will...and product to manage projects that improve the overall quality and efficiency of the client's wallet. **Responsibilities:** +… more
- AbbVie (Pleasanton, CA)
- …year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 year of related ... YouTube and LinkedIn. Job Description Key Responsibilities + Responsible for Supplier Quality Management cycle. + Primary contact with suppliers on all quality… more
- Mallinckrodt Pharmaceuticals (Sacramento, CA)
- …while ensuring work is completed and documented in compliance with the company quality system and medical device regulations. Innovation Environment: Work with ... Job Title Senior Technical Product Specialist - Medical Device Requisition JR000015165 Senior Technical Product Specialist -...we contribute to something that matters because we make quality products that impact patient lives. Our dynamic work… more
- Gilead Sciences, Inc. (Foster City, CA)
- …goals, and results to team members across functions and departments, including device development, packaging, quality , regulatory affairs and manufacturing. + ... aspirations. Join Gilead and help create possible, together. **Job Description** The Device , Packaging, and Process (DPP) function is a key component of Gilead's… more
- Cordis (Santa Clara, CA)
- …of education and experience preferred + Expertise in the FDA and International Medical Device Quality System Regulations and ISO 13485 + Six Sigma, Lean and/or ... **Responsibilities** **SUMMARY** Ensures that the products meet strict safety and quality standards. Collaborates with design and production teams to establish and… more
- US Tech Solutions (San Bruno, CA)
- …Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design/Process Verification, and Validation. ... Medical Device Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management Systems (QMS). + 3+ years of technical program… more
- Terumo Neuro (Aliso Viejo, CA)
- …data analysis. 3. Demonstrated command and knowledge of FDA and ISO medical device quality system requirements. 4. Proven experience in statistical analysis ... **12874BR** **Title:** Staff Engineer, Quality (New Products) **Job Description:** Production Support Focus...verification, and design validation. 2. Strong knowledge of medical device design control process. 3. Ability to understand the… more
- Actalent (Santa Clara, CA)
- …or equivalent combination of education and experience. * Expertise in the FDA Medical Device Quality system Regulation, MDD 93/42/EEC and ISO 13485 * Experience ... so you will get exposure to all aspects of Quality Engineering. ESSENTIAL DUTIES AND RESPONSIBILITIES + IQ, OQ,...move. + The position is responsible for ensuring that quality audit programs and regulatory submissions comply with external… more
- Amazon (Sunnyvale, CA)
- …phase, where the team investigates new processes and technologies that could impact the quality of the device , and mitigating these risks through the validation ... to everything, digital or physical. The Role: The Manager, Quality Engineering Manager (QEM) is responsible for leading a...Manager (QEM) is responsible for leading a team of Quality Engineering Managers and ensuring that our products meet… more
- ManpowerGroup (Fremont, CA)
- …in engineering or a related field with a minimum of 7 years of medical device quality assurance experience. + In-depth knowledge of quality management ... client, a leader in the healthcare industry, is seeking a Quality Engineer III to join their team. As a Quality Engineer III, you will be part of the Quality… more