Senior Manager, Engineering (Oral Solid Dosage)

Scientific Search; Chantilly (VA); On-site; USD 120,000 - 170,000; Full time

Job summary

Scientific Search seeks a Senior Manager, Engineering (OSD) to lead engineering and facilities for an Oral Solid Dosage site in Chantilly, VA. You will drive reliability, compliance, and modernization across manufacturing and packaging operations, ensuring safety and regulatory adherence.

The role demands deep OSD process knowledge, hands-on leadership in GMP environments, and a focus on CAPA, validation, and continuous improvement through Lean/Six Sigma.

Qualifications

• Experience leading engineering in OSD pharmaceutical manufacturing.
• Deep knowledge of HVAC, clean utilities, and environmental controls.
• Proven track record with validation, change control, and audits.

Responsibilities

• Lead engineering and facility operations across OSD manufacturing and packaging.
• Oversee maintenance, reliability, and performance of critical equipment.
• Manage HVAC, clean utilities, and facility systems to meet cGMP standards.
• Drive capital projects, upgrades, and infrastructure improvements.
• Ensure compliance with FDA, cGMP, and safety regulations.
• Lead root cause investigations and implement CAPA solutions.
• Champion continuous improvement using Lean and Six Sigma.

Skills

Leadership

Oral Solid Dosage

HVAC & Clean Utilities

Validation & Change Control

Regulatory Audits

GMP Environment

FMEA / HAZOP

Job description

Senior Manager, Engineering (OSD)

Location: Chantilly, VA
Step into a pivotal leadership role where you’ll shape the backbone of a high-impact pharmaceutical manufacturing site. My client is seeking a strategic engineering leader to drive reliability, compliance, and innovation across Oral Solid Dosage operations—ensuring life-saving products are delivered with precision and excellence.

Why You Should Apply

• Lead engineering strategy at a cutting-edge OSD manufacturing facility
• High-visibility role influencing operations, compliance, and capital projects
• Drive modernization, automation, and continuous improvement initiatives
• Collaborate with cross-functional leaders in a regulated, mission-driven environment

What You’ll Be Doing

• Lead engineering and facility operations across OSD manufacturing and packaging
• Oversee maintenance, reliability, and performance of critical equipment
• Manage HVAC, clean utilities, and facility systems to meet cGMP standards
• Drive capital projects, upgrades, and infrastructure improvements
• Ensure compliance with FDA, cGMP, and safety regulations
• Lead root cause investigations and implement CAPA solutions
• Champion continuous improvement using Lean and Six Sigma

About You

• Deep expertise in Oral Solid Dosage manufacturing processes and equipment
• Strong knowledge of HVAC, clean utilities, and environmental controls in pharma
• Experience with validation, change control, and regulatory audits
• Hands-on leadership in facility engineering within a GMP environment
• Skilled in risk assessments such as FMEA or HAZOP