Validation Engineer III

ManpowerGroup Global, Inc.; Town of Norway, San Diego (WI, CA); On-site; USD 44,324 - 63,128; Full time

Benefits offered by this job

Opportunity to work in a dynamic environment

Collaboration with a diverse team

Impactful projects that improve patient health

Job summary

ManpowerGroup Global, Inc. is seeking a Validation Engineer III to support validation activities in their Quality Assurance Department. The role involves leading validation protocols and managing projects in compliance with FDA and ISO standards.

The ideal candidate should possess a Bachelor's degree in a relevant field and have at least 5 years of experience in validation. Strong technical skills and the ability to communicate effectively are essential for success in this role.

Qualifications

• 5+ years of experience in validation within the medical device or related industry.
• Proficiency in equipment qualification (IQ/OQ/PQ), process validation, and computer system validation.
• Strong understanding of FDA regulations and ISO standards.

Responsibilities

• Lead and execute validation protocols for compliance with FDA and ISO standards.
• Develop and maintain validation documentation including URS, FRS, and DRS.
• Perform risk assessments and support continuous improvement initiatives.

Skills

Technical expertise

Excellent communication skills

Problem-solving

Organizational skills

Education

Bachelor's degree in Engineering, Biology, Chemistry, or related field

Job description

Our client, a leader in the medical device industry, is seeking a Validation Engineer III to join their team. As a Validation Engineer III, you will be part of the Quality Assurance Department supporting validation activities across multiple projects. The ideal candidate will demonstrate strong technical expertise, excellent communication skills, and a proactive approach to problem‑solving, which will align successfully within the organization.

Job Title: Validation Engineer III

Location: San Diego, CA

Pay Range: $39/hr on w2

What's the Job?

• Lead and execute validation protocols for equipment, processes, and systems in compliance with FDA, ISO 13485, and other relevant standards.
• Develop and maintain validation documentation including URS, FRS, DRS, FAT, DQ, IQ, OQ, PQ, PV, and related reports.
• Perform risk assessments, gap analyses, and support continuous improvement initiatives within the Quality Management System.
• Support internal and external audits by providing validation documentation and technical expertise.
• Manage validation projects, develop timelines, and communicate project status to stakeholders effectively.

What's Needed?

• Bachelor's degree in Engineering, Biology, Chemistry, or a related science field.
• At least 5 years of experience in validation within the medical device or related industry.
• Proficiency in equipment qualification (IQ/OQ/PQ), process validation, and computer system validation.
• Strong understanding of FDA regulations, ISO standards, and Good Documentation Practices.
• Excellent problem‑solving, organizational, and communication skills, with the ability to work independently and collaboratively.

What's in it for me?

• Opportunity to work in a dynamic, innovative environment supporting life‑changing diagnostics.
• Chance to contribute to high‑quality validation processes and ensure compliance with industry standards.
• Collaborate with a diverse team of experts committed to excellence and continuous improvement.
• Engage in meaningful projects that impact patient health and safety.
• Be part of a company that values diversity, inclusion, and professional growth.

If this is a role that interests you and you would like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!