Job Description We are seeking a talented Process Engineer to select inspection strategies for critical quality attributes on components. You will be responsible for completing Test Method Validation studies and generating subsequent inspection documentation. You will troubleshoot failures in TMV studies and provide appropriate solutions. You will also provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with new product development procedures. Additionally, you will lead and support capital acquisition activities from specifying equipment, contract negotiation, installation, and validation. You will lead or participate in process review meetings, participate in PFMEA, Control Plan, SOP, and PPAP generation associated with product transfers and launches, and review and approve validation documentation. Responsibilities
- Select inspection strategies for critical quality attributes on components.
- Complete Test Method Validation studies and generate subsequent inspection documentation.
- Troubleshoot failures in TMV studies and provide appropriate solutions.
- Provide engineering support for new product and process introductions.
- Lead and support capital acquisition activities from specifying equipment, contract negotiation, installation, and validation.
- Lead or participate in process review meetings.
- Participate in PFMEA, Control Plan, SOP, and PPAP generation associated with product transfers and launches.
- Review and approve validation documentation.
- Experience in regulated manufacturing industries such as medical device, aerospace, or automotive.
- Demonstrated ability to deliver project tasks on time with a focus on quality.
- Experience troubleshooting and solving engineering-related problems.
- Proficiency in using a wide variety of inspection tools and their qualification.
- Experience executing Measurement System Analysis (MSA).
- Ability to read and interpret engineering drawings and understand geometrical dimensioning and tolerancing.
- Good understanding of Design for Manufacturing (DFM), related statistical tools, and validation/verification techniques.
- Solid knowledge of manufacturing processes, materials, product, and process design.
- Bachelor's degree in Engineering or related field.
- Experience with CTQ, TMV, and remediation processes.
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following: Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fremont,CA. Application Deadline This position is anticipated to close on Jun 13, 2025. 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.
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 due to a disability, please email ... for other accommodation options.