Senior Product Engineer

Immediate need for a talented

Senior Product Engineer . This is a

12+months contract

opportunity with long-term potential and is located in

Northridge, CA(Onsite).

Job ID:26-30104
Pay Range: $51 - $52/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Key Requirements and Technology Experience:

B.S. in Mechanical, Electrical, Biomedical, or related Engineering field

Bachelor's degree or higher in Life Sciences or related discipline

Minimum 5-7 years of experience in Quality Assurance and/or Quality Systems within the medical device industry.

Experience implementing or improving ISO 13485-based QMS.

Strong experience working with Singapore medical device regulatory requirements.

Demonstrated experience supporting or leading GDPMDS/GDP certification projects.

Proven track record of successfully helping organizations obtain and maintain GDP certification

Experience interacting with certification bodies, accreditation bodies, and regulatory authorities.

5-8+ years of product engineering experience

Lead end-to-end product development activities including design, prototyping, testing, and validation

Drive technical decisions and provide engineering expertise throughout the product lifecycle

Develop and review engineering specifications, design documents, and technical reports

Identify and resolve complex engineering challenges using systematic problem-solving approaches

Cross-Functional Collaboration

Partner with R&D, Quality, Manufacturing, Marketing, and Regulatory teams to ensure alignment

Serve as a technical resource and mentor for junior engineers

Communicate technical concepts clearly to both technical and non-technical stakeholders

Lead or contribute to multiple concurrent engineering projects

Define project scope, timelines, and deliverables

Track milestones and proactively manage risks and dependencies Quality & Compliance

Ensure products meet regulatory requirements (e.g., ISO, FDA, MDR) and internal quality standards

Support design verification and validation (V&V) activities

Participate in design reviews, FMEAs, risk assessments, and change control processes

Identify opportunities to improve products, processes, and engineering practices

Apply data-driven methods to analyze performance and drive decisions

Stay current with industry trends, emerging technologies, and best practices

Our client is a leading

Medical Equipment Manufacturing Industry,

and we are currently interviewing to fill this and other similar contract positions.

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