Top 79 Manufacturing engineer Jobs in Santa Rosa, Ca

Supplier Quality Engineer
SMC Ltd. —Santa Rosa, CA
- $86,000 - $103,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- PMP
- Paid holidays
- Disability insurance
Quick Apply
Associate / Engineer Material Process
Northrop Grumman —Santa Rosa, CA
- $69,400 - $125,200 a year
- Overtime
- Microsoft Excel
- Bachelor of Science
- Mid-level
- Paid holidays
- Disability insurance
3d
Manufacturing Engineer
EnPro Industries —Santa Rosa, CA
- $89,964 - $134,946 a year
- Full-time
- Microsoft Excel
- Bachelor of Science
- Engineering
- Health insurance
- Dental insurance
8d
R&D Firmware Engineer
Keysight Technologies, Inc. —Santa Rosa, CA
- $143,000 - $238,000 a year
- Full-time
- Bachelor of Science
- System design
- 8 years
- Health savings account
- Employee stock purchase plan
Manufacturing Process Engineer
Viavi Solutions —Santa Rosa, CA
- $98,700 - $183,300 a year
- Full-time
- 5 years
- Bachelor of Science
- English
- Disability insurance
- Health insurance
6d
Machine Learning Performance Engineer
Keysight Technologies, Inc. —Santa Rosa, CA
- $160,160 - $266,930 a year
- Full-time
- Mid-level
- C++
- Health savings account
- Employee stock purchase plan
Sr. Manufacturing Engineer
Endologix —Santa Rosa, CA
- $100,000 - $115,000 a year
- Full-time
- Bachelor of Science
- Engineering
- Master's degree
- Dental insurance
- Paid time off
Electrical Engineer Wire Harness
Confidential —California
- $76 - $132 an hour
- Full-time
- Senior level
Quick Apply
8d
Senior Kinetics DE/CD Engineer
Leidos —California
- $131,300 - $237,350 a year
- Full-time
- Hybrid work
- System design
- 11+ years
- Windows
Regional Engineer
Lane Enterprises Inc —California
- $86,000 - $110,000 a year
- Full-time
- Hybrid work
- Engineering
- Mid-level
- 3 years
- Paid holidays
- Health insurance
3d
Product Design Engineer
Stäubli —Windsor, CA
- $105,000 - $135,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Research
Quick Apply
Mfg Engineer, Advanced
Keysight Technologies, Inc. —Santa Rosa, CA
- $100,850 - $168,080 a year
- Full-time
- Mid-level
- Office
- 3 years
- Health savings account
- Employee stock purchase plan
7d
Supplier Quality Engineer
Endologix —Santa Rosa, CA
- $90,000 - $102,500 a year
- Full-time
- Engineering
- Mid-level
- 3 years
- Commuter assistance
- Health savings account
Semiconductor Fab Industrial Systems Engineer
Keysight Technologies, Inc. —Santa Rosa, CA
- $124,420 - $207,370 a year
- Full-time
- Office
- 8 years
- SQL
- Health savings account
- Employee stock purchase plan
Application Engineer/Scientist
Keysight Technologies, Inc. —Santa Rosa, CA
- $118,660 - $125,340 a year
- Full-time
- Computer Science
- Mid-level
- Analysis skills
Equipment Engineer: Advanced Packaging and Die Fab
Keysight Technologies, Inc. —Santa Rosa, CA
- $80,640 - $134,400 a year
- Full-time
- Engineering
- Mid-level
- Continuous improvement
- Health savings account
- Employee stock purchase plan
Equipment Engineer: Thin Film Fab
Keysight Technologies, Inc. —Santa Rosa, CA
- $100,850 - $168,080 a year
- Full-time
- 5 years
- Engineering
- Continuous improvement
- Health savings account
- Employee stock purchase plan
Staff Optical Coating Process Engineer
Coherent Corp. —Santa Rosa, CA
- $102,178 - $138,000 a year
- Full-time
- Computer literacy
- Bachelor of Science
- Writing skills
Senior Automation/Controls Engineer
Viavi Solutions —Santa Rosa, CA
- $134,400 - $249,600 a year
- Full-time
- 5 years
- Windows
- SQL
- Disability insurance
- Health insurance
13d
Sr. Research Scientist/Engineer
Viavi Solutions —Santa Rosa, CA
- $101,500 - $188,500 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Computer skills
- Disability insurance
- Health insurance

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Supplier Quality Engineer

SMC Ltd. -
Santa Rosa, CA

Quick Apply

Job Details

Full-time
$86,000 - $103,000 a year

Benefits

Paid holidays
Disability insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Employee assistance program
Vision insurance

Qualifications

Microsoft Excel
Microsoft Outlook
Defect resolution root cause analysis
Quality control statistical data analysis
Preventive action implementation
Design of experiments
Corrective and preventive actions (CAPA)
English
ISO certification audits
Quality control audit
Minitab
Vendor compliance audits
Supplier audits
Production validation processes
Quality risk management
Medical device manufacturing facility experience
Biomedical regulatory compliance
Manufacturing
Regulatory compliance analysis
PPAP
FDA regulations
Failure analysis

Full Job Description

About Us:

SMC Ltd. is a globally recognized premium supplier to the medical market with locations throughout the world. People committed to speed, technology, and exceptional performance are the cornerstone of our organization. Comprised of dedicated people and decades of manufacturing experience, we have continued to experience strong growth and currently have outstanding career opportunities for equally dedicated people.

Job Summary:

This role ensures supplier quality at SMC Ltd. by supporting Quality Systems Management and leading strategic auditing, supplier/component development, qualification, and sourcing in collaboration with Procurement, Operations, and Quality. The position is accountable for Supplier Quality Engineering deliverables across new product development, manufacturing launch, and sustaining activities, while driving continuous improvements. Responsibilities include providing customer and supplier support through effective root cause resolution and proactive issue prevention, ensuring safe operations and overall team success. Performance is evaluated on execution, adherence to timelines, production support, quality outcomes, communication, continuous improvement, and strong cross-functional collaboration.

Essential Job Duties and Responsibilities:

Plan, conduct, and document supplier audits to ensure compliance with quality standards and regulatory requirements.
Manage supplier classification changes/updates and maintain accurate supplier records and information.
Open, track, and follow up on Supplier Corrective and Preventive Actions (CAPAs) to drive timely resolution.
Collaborate with Quality Engineers (QEs) on customer complaints related to supplier performance.
Provide Supplier Scorecard inputs to support supplier performance monitoring and evaluation.
Review, assess, and process supplier change requests in alignment with quality and regulatory requirements and in collaboration with applicable stakeholders.
Support supplier selection, classification, and initial evaluations for new and existing suppliers.
Manage Supplier PPAPs (Production Part Approval Process), including record creation in IQMS and communication with suppliers and customers.
Collaboration in the development/improvement of receiving inspection instructions/techniques of purchased parts.
Lead supplier Qualifications including (not limited to) activities such as, supplier Measurement System Analysis (MSA), tolerance and GD&T reviews, FMEA, control plans, FAI and DOE input for purchased components.
Provide inputs and collaborate on Advanced Quality Plans (APQP) to ensure robust product launches and process controls.
Contribute to the Validation Master Plan for purchased components and services, integrating supplier requirements into the overall validation strategy.
Provide Supplier Quality technical support to Program Management Department.
Collaborate in Engineering Change orders that impact purchase part or services
Identifies and addresses opportunities for improvement to supplier related processes.
Develops, maintains and updates Procedures, Work Instructions, and Forms
Point of contact for suppliers, internal and external customers for supplier related issues
Supports the ISO 13485 Business Management System through Internal Auditing.
Assist with third party and FDA quality audits as needed.
Perform other duties as assigned.

Essential Qualifications:

Bachelor’s degree in Engineering or a related technical discipline.
2–4 years of experience in a Supplier Quality role within the medical device manufacturing industry, with strong knowledge of ISO 13485:2016 and 21 CFR Part 820 requirements.
Hands-on experience with Gage R&R, CpK/PpK studies, and Design of Experiments (DoE).
Proficiency in validation/qualification activities (IQ, OQ, PQ).
Solid knowledge of risk management standards (ISO 14971) and application of risk assessment techniques such as FMEA.
Familiarity with quality processes and tools including CAPA, PPAP, Root Cause Analysis, and structured problem-solving methodologies (e.g., 8D, 5 Whys).
Experience planning and conducting supplier audits to ensure compliance with quality standards and regulatory requirements.
Strong understanding of ISO 13485 quality systems and regulatory expectations under 21 CFR 820.
Proficient in Minitab and the Microsoft Office Suite (Excel, Word, PowerPoint, Outlook).
Excellent interpersonal, verbal, and written communication skills.
Proven ability to prioritize tasks, manage time effectively, and meet deadlines.
Detail-oriented, with a strong focus on accuracy, consistency, and quality in deliverables.
Ability to read, write, and communicate effectively in English.

Desirable Qualifications:

Experience with metrology equipment, measurement methods, and inspection techniques.
Proficiency in CMM and MicroVu programming for precision measurement and validation.
Project Management training or certification (e.g., PMP or equivalent).
Six Sigma Green Belt certification or demonstrated application of Lean Six Sigma methodologies.
Certified Lead Auditor or completion of recognized lead auditor training

What SMC has to offer?

Clean, Climate-Controlled Environment
Stable schedule
Paid holiday and PTO
Health, dental, and vision insurance
401(k) retirement savings
Life and disability insurance
Promotional opportunities
Training and career growth programs
Amazing co-workers
Tuition reimbursement
Employee Assistance Program

ADA Requirements:

The employee must be able to perform medium work, exerting up to 50 pounds of force occasionally and/or negligible force frequently to move objects. This role requires extended periods of sitting while using a computer and performing repetitive motions with the wrists, hands, and fingers. Close visual acuity is necessary to prepare and analyze data, review detailed information, view a computer screen, and perform extensive reading. The employee must also have the physical capacity to stoop, kneel, crouch, reach, stand, walk, push, pull, lift, grasp, feel, and communicate as required to perform essential job functions.

We are committed to fair and equitable hiring with salaries based on relevant factors, such as work experience, education, and certifications. Toward the principle of equal pay for equal work, we post and hire within defined salary ranges. We ask all applicants to review salary ranges for each posted job opportunity, as we will not hire outside the predetermined range.

Annual Salary Range $86,000 - $103,000

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Refine Your Search

manufacturing engineer jobs in santa rosa, ca

Supplier Quality Engineer

Associate / Engineer Material Process

Manufacturing Engineer

R&D Firmware Engineer

Manufacturing Process Engineer

Machine Learning Performance Engineer

Sr. Manufacturing Engineer

Electrical Engineer Wire Harness

Senior Kinetics DE/CD Engineer

Regional Engineer

Product Design Engineer

Mfg Engineer, Advanced

Supplier Quality Engineer

Semiconductor Fab Industrial Systems Engineer

Application Engineer/Scientist

Equipment Engineer: Advanced Packaging and Die Fab

Equipment Engineer: Thin Film Fab

Staff Optical Coating Process Engineer

Senior Automation/Controls Engineer

Sr. Research Scientist/Engineer

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