Validation Engineer

Job Title : Validation Engineer

Location : Glendale, CA

Contract Length : Long-term (Initial 6 months with potential to extend up to 2 years)

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.

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)

1–4 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