Senior Manager, Engineering (Oral Solid Dosage) in Chantilly

Energy Jobline ZR; Chantilly (VA); On-site; USD 180,000 - 230,000; Full time

Job summary

Energy Jobline ZR is seeking a Senior Manager, Engineering (OSD) in Chantilly, VA to lead reliability, compliance, and modernization at a GMP pharmaceutical site.

You will drive capital projects, oversee HVAC and clean utilities, and ensure FDA/cGMP adherence while mentoring cross-functional teams.

This role requires hands-on leadership in a regulated environment with a track record in Lean and Six Sigma initiatives.

Qualifications

• Deep expertise in Oral Solid Dosage manufacturing 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.

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

Oral Solid Dosage

HVAC & clean utilities

Regulatory audits

Validation & change control

GMP leadership

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