Quality Engineer III

ManpowerGroup Global, Inc.; Santa Clara (CA); On-site; USD 47,000 - 63,000; Full time

Benefits offered by this job

Medical plans

Dental plan

Vision plan

Health Savings Account (HSA)

Flexible Spending Account (FSA)

Dependent Care FSA

Life Insurance

Disability Insurance

Travel Insurance

401(k) with match

Weekly pay

Job summary

ManpowerGroup Global, Inc. is seeking two dedicated Quality Engineer III professionals for a 12-month contract in Santa Clara, CA. The role supports manufacturing, integration, and testing of engineered-to-order bioprocessing equipment and automation systems.

The ideal candidate has 4+ years in Quality Engineering within regulated manufacturing, strong problem-solving and communication skills, and hands-on experience with cGMP and ISO standards. $40/hr; long-term extension possible.

Qualifications

• Bachelor’s degree in engineering or related technical field required.
• 4+ years in Quality Engineering or similar in regulated manufacturing.
• Hands-on quality support on equipment assembly, testing, and documentation.

Responsibilities

• Serve as the primary Quality Engineering partner for manufacturing, integration, and testing activities.
• Collaborate with Manufacturing, Engineering, Automation, Project Management, and Supply Chain to meet quality requirements.
• Provide hands-on quality support on the production floor addressing real-time issues.
• Support quality readiness for IQ/OQ/PQ and customer acceptance activities.
• Develop and maintain SOPs, work instructions, and quality records compliant with cGMP and ISO standards.

Skills

Problem-solving

Communication

Attention to detail

Quality systems knowledge

Education

Bachelor's degree in Mechanical, Process, Electrical, Automation, Biomedical Engineering

Job description

Our client, a leader in the bioprocessing equipment manufacturing industry, is seeking twodedicated and detail-oriented Quality Engineer III's to join their dynamic team. As a Quality Engineer III, you will be an integral part of the Quality department supporting manufacturing, integration, and testing activities. The ideal candidate will demonstrate strong problem-solving skills, excellent communication, and a proactive approach to quality assurance, aligning seamlessly with the organization’s commitment to excellence and continuous improvement.

Job Title:Quality Engineer III (2 openings)

Location:Santa Clara, CA

Pay Rate:$40/hr.

Job Type:12-month contract with the potential for hire/extension

Schedule: M-F 40 hrs./wk.

What's the Job?

• Serve as the primary Quality Engineering partner for manufacturing, integration, and test activities supporting engineered-to-order bioprocessing equipment and automation systems.
• Collaborate with Manufacturing, Engineering, Automation, Project Management, and Supply Chain teams to ensure quality requirements are met throughout project execution, including build, integration, FAT, and release.
• Provide hands-on quality support on the production floor, addressing real-time quality issues related to equipment assembly, wiring, tubing, automation configuration, testing, and documentation.
• Support quality readiness for HAT/FAT and customer acceptance activities, including review of build records, test documentation, and release packages, and perform or support IQ, OQ, PQ activities.
• Develop, maintain, and approve SOPs, work instructions, templates, and quality records in compliance with cGMP, ISO 9001, and ISO 13485 standards.

What's Needed?

• Bachelor of Science degree in Mechanical, Process, Electrical, Automation, Biomedical Engineering, or a related technical field.
• 4+ years of experience in Quality Engineering or a related technical role within a regulated manufacturing environment.
• Hands-on experience supporting engineered-to-order bioprocessing or capital equipment, including mechanical assembly, electrical/automation integration, and testing activities.
• Strong knowledge of cGMP principles and quality standards such as ISO 9001, ISO 13485, ISO 14971, and ISO 17025.
• Proficiency with site Quality Management Systems, including Document Control, CAPA, Deviations, Nonconformance, Change Management, and Auditing.

What's in it for me?

• Opportunity to work in a cutting-edge manufacturing environment supporting innovative bioprocessing solutions.
• Engage in meaningful projects that impact global health and biomanufacturing advancements.
• Collaborate with a diverse and talented team committed to quality and continuous improvement.
• Develop your skills through exposure to industry standards and regulatory compliance processes.
• Be part of a company that values integrity, accountability, and professional growth.

Upon completion of waiting period consultants are eligible for:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account
• Health Flexible Spending Account
• Dependent Care Flexible Spending Account
• Supplemental Life Insurance
• Short Term and Long Term Disability Insurance
• Business Travel Insurance
• 401(k), Plus Match
• Weekly Pay