Job Title: Sr. Quality Engineer

Job Description

Working as a quality engineer in the R&D department - Wafer and Sensor Operations and Hybrid product lines. In this Quality Engineer for Operations Quality, you will have responsibility for the Quality and Compliance of process development and manufacturing of implantable electronic products at our Tempe Campus. Responsibilities may include the following and other duties may be assigned. Ensure internal quality processes, procedures, and systems are compliant with all governing standards. Support manufacturing development and continuous improvement as the Quality team member for process development and validation including Equipment Development, IQ, Process Characterization, and Test Method Development and Validation. Use knowledge of statistics on acceptance criteria, DOE, and comparison testing to support manufacturing engineers in the development of compliant test plans and reports. Support risk assessment processes for manufacturing and development including process FMEA and design FMEA, ensuring risk assessments are thorough and documentation meets all governing requirements. Support CAPA investigations, improvements, and effectiveness verification testing. Lead and/or support investigations of non-conforming product, materials, or processes through the coordination of cross-functional teams while simultaneously performing the role of Quality Engineer. The Principal Manufacturing Quality Engineer is responsible for documentation of the non-conformances, identification of the population, containment of the population, and communication of non-conformance to applicable parties. Independently provide comprehensive technical solutions for complex issues related to quality processes, procedures, and systems to meet organizational objectives. Facilitate group meetings and project leaders.

Hard Skills

• Strong back ground in Equipment Development

• 4+ years working in medical device or with wafer/electronic components

• IQ, Process Characterization, and Test Method Development and Validation

• Strong understanding of regulatory requirements, i.e.: FDA-GMP

• BS engineering degree or technical degree

Soft Skills

• Effective communication

• Team collaboration

• Attention to detail

• Problem-solving

• Leadership

Job Type

This is a contract position with a duration of 12 Month(s).

Work Site

This is a fully on-site position in Tempe, Arizona.

Work Environment

Mon-Fri 8am-5pm (In office). Office setting/manufacturing floor.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent

• Maintaining an inclusive environment through persistent self-reflection

• Building a culture of care, engagement, and recognition with clear outcomes

• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.