• Union City
• US$130000 - US$170000 per year + Bonus
• Posted 4 days ago

Senior Systems Engineer | 140k-170k + Bonus| Medical Devices Company Introduction We are looking for a Senior/Principal Systems Engineer, title is flexible, for one of our medical device clients. Our client is constantly growing and in NPD, this candidate can have career growth opportunities into...

• Alameda
• US$130000.00 - US$165000.00 per year + Bonus
• Posted 4 days ago

Senior Electrical Test Engineer | 130k-165k + Bonus| Innovated Electromechanical Start Up Company Intro We are looking for a Senior Electrical Test Engineer for one of our medical device clients. They are a start up company that was recently acquired, and based off previous success they are start...

• Irvine
• Negotiable
• Posted 12 days ago

This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. General Description and Duties: To perform this job successfully, an...

• Brisbane
• US$120000 - US$135000 per year
• Posted 17 days ago

The Sr. Quality Engineer will be responsible for facilitating QMS implementation, ensure conformance to regulatory compliance / customers, and oversee component qualification from suppliers.

• Brisbane
• US$95000 - US$115000 per year
• Posted 17 days ago

The Quality Systems Engineer (PMS) will be responsible for ensuring compliance of the QSR to all applicable regulations and standards & working cross-functionally with various teams to execute the transition EU Medical Device Directive to EU Medical Device Regulation. Requirments: B.S., Life Scie...

• Brisbane
• US$90000 - US$105000 per year
• Posted 17 days ago

The Quality Specialist (Complaint Handling) will be responsible for investigation and reviewing all product complains and take appropriate corrective action(s) aligned with regulatory and QSR requirements. Requirements: B.S., Life Science, Engineering, or related 1-2 years industry experience Reg...

• Irvine
• Negotiable
• Posted 17 days ago

Title: Complaint & CAPA Coordinator Department: Quality Assurance Reports to: Director of QA/RA Direct Reports: N/A JOB SUMMARY: Ensures that the company's products consistently meet or exceed established quality standards. Responsible for day to day Quality System processes and tasks including C...

• Brea
• Negotiable
• Posted 17 days ago

Job Title: Manufacturing Engineer Department: Manufacturing ESSENTIAL FUNCTIONS AND RESPONSIBILITIES include the following. Execute remediation validation/ verification activities such as: Installation Qualification (IQ), Operations Qualification (OQ), Process Qualification (PQ)/Process Performan...

• San Diego
• Negotiable
• Posted 17 days ago

Job Title: Regulatory Affairs Specialist I-III Status: Exempt Location: San Diego, CA (Hybrid) Austin Vita is delighted to support a worldwide diagnostic company based in San Diego, who is looking for a Regulatory Affairs specialist to join a growing team. Job Summary The Regulatory Affairs Speci...

• Valencia
• US$120000.00 - US$150000.00 per year
• Posted 18 days ago

The Systems Engineer is responsible for solutions, architecture, and requirements management of an electronic medical device system. This position leads collaboration efforts for requirements analysis and test documentation, including all related Requirements Specification, Design Description, Te...

• San Diego
• US$150000.00 - US$170000.00 per year
• Posted 18 days ago

The QA Manager is responsible for overseeing the activities of their assigned team(s) and individually performing tasks to ensure the effectiveness of the Quality Systems. This position manages work assignments and processes to meet productivity standards, quality goals and department objectives....

• San Diego
• US$12000.00 - US$150000.00 per year
• Posted 18 days ago

Job Summary The Senior Quality Engineer is an advanced level position that works with cross-functional teams to ensure product and processes meet specifications and operate within claims and control parameters in alignment with Quality Management Systems (QMS) requirements. This position works wi...

• Irvine
• US$110000.00 - US$130000.00 per year
• Posted 18 days ago

The primary responsibility of the lead regulatory affairs specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies. The incombant is also responsible for ensuring products and procedures comply with regulatory agency specifications. Supports necessary...

• Carlsbad
• US$90000 - US$120000 per year
• Posted 19 days ago

Project Manager The Project Manager is responsible for supporting the delivery of the programs within R&D. They will ensure project plans are consistently tracked and maintained through close collaboration and communication with team leaders. Utilizing their project management expertise, they wil...

• Fremont
• US$120000 - US$165000 per year
• Posted 21 days ago

The Program Manager will be responsible for projects at all stages of the lifecycle including: project planning, documentation throughout research and development, maintaing customer needs, facilitating communication amongst teams, conducting feasability studies, risk assessment and analysis, con...

• Fremont
• US$130000 - US$160000 per year
• Posted 22 days ago

The NPI Program Manager will be in charge of the budget, timeline, and technical aspects of various projects. They will work with external/internal teams and operate as the main poc with the customers, as well as be an active part of new business development.

• Tustin
• US$120000.00 - US$160000.00 per year
• Posted 2 months ago

Senior Scientist (NGS Assay Development) Primary Job description Leads projects. Provides technical review, direction, and feedback to others. Conducts advanced research. Core Job Responsibilities Design and conduct routine to complex experimental procedures within the overall scope of a research...

• San Clemente
• Negotiable
• Posted 3 months ago

Job Title: Director of Regulatory Affairs Austin Vita is delighted to support a premier weight-loss solutions company based in Orange County who is hiring for a Director Regulatory Affairs to join a growing team. Located in San Clemente, this position offers a hybrid work environment. Job Descrip...

• Fremont
• US$130000 - US$150000 per year
• Posted 3 months ago

This cross-functional position will operate as the Quality rep. on current and new product development, focusing largely on design & risk assessment / analysis and requiring a very strong technical skillset. The SQE will be responsibile for developing and continually improving standard practices ...

• Brisbane
• US$115000 - US$135000 per year
• Posted 7 months ago

The Design Quality Assurance Engineer will respresent Quality and work with Regulatory, Operations, and R&D for all design control and product development related activities.