Pharma Manufacturing Engineer: System Owner & MMP Lead

Mirus Consulting Group; Juncos (PR); On-site; USD 80,000 - 120,000; Full time

Job summary

mîrus Consulting Group, a local Humacao, Puerto Rico firm, is seeking an experienced Engineer to provide engineering support for manufacturing and facilities operations within a regulated pharmaceutical/biotech environment.

The successful candidate will serve as a system owner, support maintenance and reliability initiatives, coordinate vendor activities, manage purchase orders, and ensure compliance with cGMP while supporting continuous operations.

Qualifications

• Master’s degree in Engineering or Bachelor’s degree with 2+ years in engineering.
• Experience as System Owner in regulated manufacturing environments.
• Experience with MMP activities and cGMP procedures.
• Experience using Maximo or similar CMMS.
• Experience creating and processing Purchase Orders (POs).
• Experience coordinating vendors in regulated facilities.
• Strong project management and multi-tasking abilities.

Responsibilities

• Serve as System Owner for manufacturing/utility systems with reliability focus.
• Support Maintenance Management Program activities and documentation.
• Apply cGMP requirements to pharma/biotech production processes.
• Utilize Maximo to manage assets, maintenance, and docs.
• Create, process, and track Purchase Orders.
• Coordinate, escort, and oversee vendors/contractors on site.
• Support troubleshooting, investigations and continuous improvement.
• Manage multiple projects and priorities with deadlines.
• Collaborate with Manufacturing, Quality, Maintenance, Validation and Supply Chain.

Skills

System Owner

Vendor coordination

Maintenance Management Program

Project management

cGMP compliance

Multi-tasking

Problem-solving

Communication skills

Education

Master’s degree in Engineering

Bachelor’s degree in Engineering

Tools

Maximo

Job description

mîrus Consulting Group, a local Humacao, Puerto Rico firm, is seeking an experienced Engineer to provide engineering support for manufacturing and facilities operations within a regulated pharmaceutical/biotech environment.

The successful candidate will serve as a system owner, support maintenance and reliability initiatives, coordinate vendor activities, manage purchase orders, and ensure compliance with cGMP while supporting continuous operations.