Overview:

We’re seeking a Validation Engineer with 2–5 years of experience in the pharmaceutical or life sciences industry to support validation and qualification activities across multiple client sites. This role is ideal for a hands-on professional who enjoys a mix of technical work, client interaction and travel.

Key Responsibilities:

• Execute and document validation activities (IQ/OQ/PQ) for equipment, systems, utilities, and processes.

• Support development and review of validation protocols, reports, and related documentation.

• Ensure compliance with FDA, GMP, and company quality standards.

• Collaborate with cross-functional teams to support commissioning and qualification projects.

• Troubleshoot validation issues and provide recommendations for corrective actions.

Qualifications:

• Bachelor’s degree in Engineering, Life Sciences, or related discipline.

• 2–5 years of validation experience within pharmaceutical, biotech, or regulated environments.

• Strong knowledge of GMPs, FDA, and industry validation standards.

• Excellent communication and documentation skills.

Location: Greater Boston, Philadelphia, Raleigh-Durham, or other Eastern Seaboard locations

Travel: Ability to travel up to 80% for project assignments along the East Coast

Employment Type: Full-Time (Direct Hire)

Sponsorship: Not available (No visa sponsorship or extensions)