Equipment Engineer
Scientific Search is looking for Equipment Engineer in Fairfax Station, VA.
This local job opportunity with ID 3673971943 is live since 2026-05-12 11:47:49.
Location: Chantilly, VA
Step into a high-impact engineering role where your work directly supports the production of safe, reliable, and affordable medicines. This opportunity places you at the center of pharmaceutical manufacturing operations, influencing equipment performance, compliance, and process optimization across the full system lifecycle. If you thrive in regulated environments and enjoy seeing your engineering decisions translate into real-world outcomes, this role delivers.
Why You Should Apply
Location: Chantilly, VA
Step into a high-impact engineering role where your work directly supports the production of safe, reliable, and affordable medicines. This opportunity places you at the center of pharmaceutical manufacturing operations, influencing equipment performance, compliance, and process optimization across the full system lifecycle. If you thrive in regulated environments and enjoy seeing your engineering decisions translate into real-world outcomes, this role delivers.
Why You Should Apply
- Play a critical role in ensuring the quality and integrity of life-saving pharmaceutical products
- Work across R&D, manufacturing, packaging, and quality teams on meaningful projects
- Hands-on ownership of equipment qualification, validation, and optimization
- Exposure to capital projects and system lifecycle engineering in a regulated setting
- Oversee, maintain, and evaluate manufacturing and utility equipment
- Lead IQ/OQ/PQ activities and execute validation protocols
- Develop and review SOPs, change controls, and qualification documentation
- Support audits and ensure compliance with FDA and cGMP regulations
- Drive equipment improvements and process optimization initiatives
- Partner cross-functionally with vendors, contractors, and internal teams
- Bachelors degree in Mechanical or Industrial Engineering (Masters preferred)
- Hands-on experience with IQ/OQ/PQ and equipment validation
- Working knowledge of FDA regulations, cGMP, and Part 11
- Familiarity with CAPA, PLCs, and pharmaceutical manufacturing systems