Pharmaceutical Maintenance Engineer; Oral Solid Dosage

Pharmaceutical Maintenance Engineer (Oral Solid Dosage)

Granules Pharmaceuticals Inc. (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and are currently the 10th fastest growing generic pharma company in the US. With sites in Chantilly and Manassas, Virginia, we are involved in R&D and manufacturing of generic drugs including pulsatile drug release tablets and capsules, orally disintegrating modified‑release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to provide customers reliable and affordable options.

We are seeking a skilled and proactive Maintenance Engineer with experience in the oral solid dosage (OSD) pharmaceutical industry
. The ideal candidate will be responsible for ensuring reliable operation, maintenance, and continuous improvement of manufacturing equipment and facility systems to support safe, compliant, and efficient production.

• Perform preventive, predictive, and corrective maintenance on solid oral dosage equipment, including:
  • Blenders, granulators, and mills
  • Tablet presses and capsule fillers
  • Coating machines
  • Packaging lines (bottle, blister, cartoner)
• Troubleshoot mechanical, electrical, pneumatic, and automation issues to minimize downtime.
• Support equipment installation, commissioning, qualification (IQ/OQ), and validation activities.
• Maintain accurate maintenance records, work orders, and equipment logs in the CMMS system.
• Ensure all maintenance activities comply with cGMP, safety, and regulatory requirements.
• Collaborate with Production, Quality, and Engineering teams to resolve equipment‑related issues.
• Participate in root‑cause analysis (RCA) and implement corrective and preventive actions (CAPA).
• Identify opportunities for equipment upgrades, reliability improvements, and process optimization.
• Support audits, inspections, and documentation requests from QA and regulatory bodies.
• Ensure spare parts inventory is maintained and managed effectively.

• Bachelor’s degree in mechanical, electrical, industrial, or related engineering field (or equivalent experience).
• 4+ years of maintenance experience in a pharmaceutical oral solid dosage manufacturing environment.
• Strong understanding of cGMP, FDA, and safety regulations.
• Hands‑on experience with tablet compression, encapsulation, granulation, and coating equipment.
• Ability to read mechanical drawings, electrical schematics, and equipment manuals.
• Experience with CMMS systems and maintenance documentation.
• Strong troubleshooting, analytical, and problem‑solving skills.
• Ability to work independently and in cross‑functional teams.

• Experience with automation systems (PLC, HMI, SCADA).
• Knowledge of HVAC, compressed air, and utility systems.
• Familiarity with lean manufacturing and reliability engineering principles.

• Mid‑Senior level

• Full‑time

• Management and Manufacturing

• Software Development

Chantilly, VA, United States