Pharma Manufacturing Engineer — 24/7 Operations

Quality Consulting Group, LLC; Juncos (PR); In loco; USD 80.000 - 110.000; Tempo pieno

Descrizione del lavoro

Quality Consulting Group, LLC is seeking a talented engineer to support daily manufacturing operations in a world-class facility in Puerto Rico and the USA.

The role requires a Bachelor’s degree in Engineering and hands-on experience with regulated pharma/biotech equipment, CAPAs, and IBM Maximo. You will collaborate across Manufacturing, Maintenance, Process Development, QA, and Validation teams to drive process improvements.

Competenze

• Bachelor’s degree in Engineering in a related field.
• Experience supporting manufacturing equipment in regulated pharma/biotech.
• Knowledge of system owner assessments, CAPAs, and investigations.
• Experience with IBM Maximo for work orders and preventive maintenance.
• Ability to troubleshoot equipment failures and improve reliability.
• Experience developing preventive maintenance strategies and SOPs.

Mansioni

• Provide technical engineering support to daily manufacturing operations.
• Serve as a technical resource for equipment, processes, and systems.
• Monitor processes, identify issues, and propose solutions.
• Collaborate with cross-functional teams on process improvements.
• Support deviations, qualifications, validation, training, and NPI activities.
• Analyze data and present findings for projects.
• Ensure GMP/GLP compliance and regulatory expectations.
• Support 24/7 manufacturing operations including non-standard shifts.

Conoscenze

Troubleshooting

Root cause analysis

Cross-functional collaboration

Documentation

Formazione

Bachelor’s degree in Engineering

Strumenti

IBM Maximo

Descrizione del lavoro

Quality Consulting Group, LLC is seeking a talented engineer to support daily manufacturing operations in a world-class facility in Puerto Rico and the USA.

The role requires a Bachelor’s degree in Engineering and hands-on experience with regulated pharma/biotech equipment, CAPAs, and IBM Maximo. You will collaborate across Manufacturing, Maintenance, Process Development, QA, and Validation teams to drive process improvements.