Senior R&D Technician

Manpower; Temecula (CA); On-site; USD 70,000 - 110,000; Full time

Job summary

Manpower is seeking an experienced Senior R&D Technician to bridge early-stage medical device design with physical realization in Temecula, CA. The role focuses on assembling complex prototypes, refining processes, and contributing to design feedback for engineering partners.

The ideal candidate has 5–10 years in medical device manufacturing, strong mechanical and interpretation skills, and hands-on experience with laser welding, soldering, and bench testing.

Qualifications

• 5–10 years of experience in medical device manufacturing.
• High School Diploma (or equivalent) or significant hands-on experience.
• Familiarity with medical device equipment/techniques (e.g., laser welding, plastic processing, soldering, bench testing, and precision inspection).
• Ability to read and interpret engineering drawings and manufacturing documentation.

Responsibilities

• Prototype assembly of complex medical device prototypes and development of assembly methods and processes.
• Design and develop custom tooling and fixtures to support scalable production.
• Read and interpret complex engineering drawings and provide actionable feedback to refine designs.
• Own lab equipment, calibration, and maintenance responsibilities.
• Work within strict quality-controlled environment procedures and guidelines.
• Document progress and draft clear updates for client meetings.

Skills

Mechanical comprehension

Interpret engineering drawings

Basic arithmetic

MS Office

Teamwork

Self-directed

Education

High School Diploma

Tools

Laser welding

Plastic processing

Soldering

Bench testing

Precision inspection

Job description

We are seeking an experienced and self-motivated Senior R&D Technician to join our engineering team. In this role, you will act as a key hands-on bridge between early-stage product design and physical realization, helping develop, assemble, and optimize complex medical device prototypes and manufacturing processes.

As a Senior Technician, you will be expected to operate and maintain laboratory equipment to support novel Medical Device prototypes, offer valuable design feedback to engineering partners, and maintain high standard compliance within a quality-controlled environment.

Key Responsibilities

• Prototype Assembly & Process Development: Build high-quality, complex medical device prototypes. Assist engineers in defining assembly methods, developing processes, and drafting technical documentation.
• Tooling & Fixturing: Design and develop custom manufacturing tooling and fixtures to support production scalability.
• Design & Technical Feedback: Read and interpret complex engineering drawings and manufacturing instructions, offering actionable feedback to refine prototype designs.
• Lab & Equipment Ownership: Serve as the subject matter expert for laboratory equipment and instruments—managing maintenance, calibration, and optimal usage.
• Controlled Environment & Quality Systems: Work independently and within teams under strict quality-controlled environment procedures and guidelines.
• Documentation & Communication: Maintain precise records (e.g., laboratory notebooks) and draft clear progress updates to support client meetings. Maintain a professional demeanor during complex client interactions.

Qualifications & Skills

Required:

• Experience: 5–10 years of experience in medical device manufacturing or a closely related technical industry.
• Education: High School Diploma (or equivalent) or significant equivalent hands-on experience.
• Technical Skills: Familiarity with medical device equipment/techniques (e.g., laser welding, plastic processing, soldering, bench testing, and precision inspection).
• Core Competencies: Strong mechanical comprehension, basic arithmetic, and the ability to interpret technical drawings and manufacturing documentation.
• Software: Proficient with MS Office applications.
• Professional Attributes: Self-directed with minimal supervision required; highly organized, mature, responsible, and a collaborative team player.
• Prior experience working within an assembly line setting.
• Experience navigating regulated Medical Device Quality Management Systems (QMS).

Physical Requirements & Working Conditions

• Cleanroom Access: Ability to enter and exit a Controlled Environment Room (CER) regularly.
• Precision Work: Ability to work under a microscope for extended periods.
• Physical Effort: Ability to sit for extended periods and lift up to 50 lbs.
• Mobility: Willingness to travel as required between primary operating locations and other designated sites.