Pharma Equipment Engineer: Validation & Compliance

Scientific Search; Chantilly (VA); On-site; USD 60,000 - 80,000; Full time

Job summary

A staffing and recruiting firm is seeking an entry-level engineer in Chantilly, VA to oversee and maintain pharmaceutical manufacturing equipment. The role involves leading validation activities, ensuring compliance with FDA regulations, and driving process optimization. Candidates with a Bachelor's in Mechanical or Industrial Engineering and experience in IQ/OQ/PQ are encouraged to apply. This full-time position is essential for producing safe and reliable medicine.

Qualifications

• Experience with equipment validation including IQ/OQ/PQ.
• Understanding of FDA regulations, cGMP, and Part 11.
• Familiarity with CAPA and PLCs in a manufacturing context.

Responsibilities

• Oversee and maintain manufacturing equipment.
• Lead validation activities and execute protocols.
• Develop and review standard operating procedures (SOPs).
• Support audits and ensure compliance with regulations.
• Drive equipment improvements and process initiatives.

Skills

IQ/OQ/PQ experience

FDA regulatory knowledge

Process optimization

SOP development

Cross-functional collaboration

Education

Bachelor’s degree in Mechanical or Industrial Engineering

Master’s degree (preferred)

Job description

A staffing and recruiting firm is seeking an entry-level engineer in Chantilly, VA to oversee and maintain pharmaceutical manufacturing equipment. The role involves leading validation activities, ensuring compliance with FDA regulations, and driving process optimization. Candidates with a Bachelor's in Mechanical or Industrial Engineering and experience in IQ/OQ/PQ are encouraged to apply. This full-time position is essential for producing safe and reliable medicine.