Process Specialist

Our client is seeking a Process Validation Engineer to support multi-client manufacturing operations in a regulated cGMP CDMO environment. This role partners closely with Manufacturing, Engineering, and QA to ensure robust, compliant, and scalable processes across diverse customer programs.

Shift: Monday–Friday, 8:00am–5:00pm

Pay: $34–$38.50/hour

• Execute and document process validation activities (PPQ, IQ/OQ/PQ) for equipment, processes, cleaning, and utilities.
• Write validation protocols and reports for customers in support of tech transfer, scale-up, and routine manufacturing.
• Support process engineering activities, including defining CPPs/CQAs and maintaining validated state across multiple client products.
• Author and maintain SOPs, templates, and validation documentation to ensure audit readiness.
• Review manufacturing, analytical, and microbial data; support deviations, investigations, and CAPAs.
• Provide technical support during client and regulatory audits.

• Bachelor’s degree in Chemical, Mechanical, or related Engineering field.
• 1–3 years of experience in process validation, process engineering, or manufacturing support in a cGMP environment (CDMO experience preferred)

• Associate

• Full-time

Personal Care Product Manufacturing

Medical insurance

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