Senior Design Quality Engineer
Spectraforce
Irvine, California
2 hours ago
Job Description
Position Title: Senior Design Quality Engineer
Work Location: Irvine, CA 92614
Assignment Duration: 18 Months
Work Arrangement: Onsite
Position Summary: As part of our Quality Engineering team, you will work closely with our R&D and Manufacturing teams to develop the latest tools and technologies to address significant, unmet clinical needs that impact patients’ lives around the world.
Key Responsibilities:
Qualification & Experience:
Additional Information:
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 54.00/hr.
Work Location: Irvine, CA 92614
Assignment Duration: 18 Months
Work Arrangement: Onsite
Position Summary: As part of our Quality Engineering team, you will work closely with our R&D and Manufacturing teams to develop the latest tools and technologies to address significant, unmet clinical needs that impact patients’ lives around the world.
Key Responsibilities:
- Perform Quality Engineering activities related to product development and ongoing cleanroom build support
- Ensure NPD processes comply to quality system and applicable regulatory standards.
- Update risk management and design control files. Maintain relevant quality documentation.
- Develop and execute test methods validations and qualification plans.
- Support design verification and facilitate process validation and commercialization activities related to multi-site transfer.
- Work collaboratively with cross-functional teams, including R&D, manufacturing, regulatory, clinical, and marketing.
- Other duties assigned by Leadership.
Qualification & Experience:
- Bachelor’s degree in engineering or Scientific field & 4+ years' experience -OR- Master's Degree or equivalent in Engineering or Scientific field & 3+ years' experience
- Proficient understanding of medical device operations and/or manufacturing processes. Medical Device experience strongly preferred.
- Relevant experience in product development, quality assurance, and/or related fields
- Knowledge and understanding of Engineering and Quality principles, theories, and concepts
- Understanding of ISO 13485
- Experience developing, updating, and maintaining technical content of risk management files
- Basic understanding of statistical techniques. Experience using statistical software (i.e. Minitab) a plus.
- Experience in test method development including validation and/or fixture development
- Solid problem-solving, organizational, analytical, and critical thinking skills
- Good documentation and communication (e.g., written and verbal) skills with keen attention to detail
- Ability to build productive working relationships and interact professionally with all organizational levels
- Ability to manage competing priorities in a fast-paced environment
Additional Information:
- Strong preference: candidates with previous experience in NPD, Design Assurance (DA), Quality Engineering.
- Role will not be for full time conversion.
Applicant Notices & Disclaimers
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 54.00/hr.