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YO AI Labs in Chantilly, VA, USA is seeking a Senior Manager, Engineering (OSD) to oversee equipment reliability, facility systems, and continuous improvement in a cGMP environment.
You will lead engineering teams across OSD manufacturing, packaging, and utilities, drive CAPA and reliability initiatives, and ensure regulatory compliance with FDA and OSHA standards. A strong background in HVAC, clean utilities, and environmental controls is required.
This role oversees equipment reliability, facility systems, utilities, capital projects, and continuous improvement initiatives while ensuring full compliance with cGMP, safety, and regulatory standards. The ideal candidate brings deep technical expertise in OSD processes and strong knowledge of facility engineering, including HVAC, clean utilities, building systems, and environmental controls.
Mentor and develop engineering and facility staff, fostering technical growth and leadership capability.
Build a collaborative, high performance engineering organization.
12+ years of engineering experience in pharmaceutical Oral Solid Dosage (OSD) manufacturing.
Deep technical knowledge of OSD equipment (granulators, fluid bed dryers, tablet presses, capsule fillers, coaters, packaging lines) and facility infrastructure (HVAC, cleanrooms, clean utilities, chilled water, boilers).
Demonstrated track record leading and developing larger engineering and facilities operations.
Candidates must have strong, hands-on experience in US-based facilities and operations. Direct familiarity with US regulatory standards, local permitting requirements, building codes, OSHA regulations, and FDA cGMP compliance is mandatory
Bachelor's degree in mechanical, Chemical, Electrical Engineering, or related field.12+ years of engineering experience in pharmaceutical OSD manufacturing.
Strong knowledge of facility engineering, including HVAC, clean utilities, building systems, and environmental controls.
Proven leadership experience managing engineering and facility teams.
Deep understanding of cGMP, validation, and regulatory requirements.