Validation Engineer | Glendale, CA | Onsite

Title: Validation Engineer

Location: Glendale, CA (Local Candidates Only)

Duration: 6-12+ months

Overview:

• A leading pharmaceutical manufacturer in Glendale, CA is seeking multiple Validation Engineers to support ongoing capital projects. We are targeting local candidates only who can hit the ground running-strong validation protocol writing and execution skills are a must.

• This is a great opportunity for early-career professionals (1 4 years of experience) who want to contribute to long-term, high-impact projects in a regulated environment.

Key Responsibilities:

• Write and execute IQ/OQ protocols for equipment such as centrifuges, filter presses, and processing tanks
• Perform installation qualifications and support equipment validation activities
• Collaborate with engineers during job walks for capital projects
• Prepare and maintain accurate technical documentation in compliance with regulatory standards
• Coordinate with cross-functional teams to meet validation timelines and ensure project alignment
• Communicate effectively with project stakeholders and team members
• Support multiple validation efforts simultaneously while maintaining high-quality standards

Qualifications:

• BS degree in Engineering, Life Sciences, or related field (required)
• 2 4 years of Validation Engineering experience in the pharmaceutical industry
• Strong experience with equipment validation and technical writing
• Familiarity with GMP environments and FDA expectations
• Excellent communication and organizational skills
• Positive attitude and ability to multi-task in a fast-paced project setting
• Must be committed to supporting a long-term engagement

Best regards,

Lavesh Kumar

| Sr. Technical Recruiter

STELLENT IT A Nationally Recognized Minority
Certified Enterprise

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