Benefits:

401(k) matching

Company parties

Competitive salary

Dental insurance

Free food & snacks

Health insurance

Opportunity for advancement

Paid time off

Training & development

Vision insurance

BridgeMed Solutions, Inc is seeking a Project Manager. Training will be provided.

Are you passionate about pioneering medical innovations? Join our dynamic team at BridgeMed Solutions, where we're revolutionizing healthcare through cutting-edge technology. We are an Irvine-based Contract Manufacturing Organization that is ISO and FDA certified. We are a privately owned company that specializes in tissue heart valve technology. We additionally custom produce transcatheter valves for various clients. Embrace the opportunity to make a meaningful impact on patient care while collaborating with talented professionals in a fast-paced startup environment. Apply now and be part of our journey towards transforming lives.

The Project Manager should have a background as an engineer with general knowledge of engineering principles and be responsible for providing engineering support for products from design through commercialization. Responsibilities will include the design of products, prototypes, subassemblies, design for manufacturability, design for verification, establishing critical dimensions, validation of manufacturing processes, client and vendor Management.

Job Title: Project Manager

Experience: 2-4 years industry experience

Location: Irvine, CA

Job Type: Full Time, 100% In-House

Salary: $60000 - $75000

Benefits: PTO, Sick days, Holiday Pay, 401k, Health-Vision-Dental Coverage, Free Lunch Fridays, Company Parties

Position Responsibilities

· This position will provide support in the design, development, testing, and refinement system, sub-system, and components for medical devices, manufacturing equipment, etc.

· Design and develop medical devices, and procedures using the principles of engineering and biological sciences

· Design, development, and verification/validation testing of medical products for CE mark submissions / FDA submissions

· Research, document, organize, prepare, and present the materials for internal knowledge transfer

· Accountable for all record-keeping as necessary

· Manage product design during product development

· Develop and control prototypes, laboratory testing, design refinement, design verification/validation, and documentation

· Perform necessary engineering analysis as-needed basis.

· Prepares plans, and schedules, and manages projects.

· Performs other duties as assigned

Basic Qualifications:

B.S. degree in Mechanical Engineering

3+ years of client management

3+ years of design and development

Oral and written communication skills

Solidworks / Cadcam is a plus

Vendor relations is a plus

Heart Valve assembly is a plus