Pharma Process Engineer: Troubleshooting & Optimization (PR)

Inteldot; Puerto Rico; On-site; USD 80,000 - 110,000; Full time

Job summary

Inteldot is seeking an engineering professional to optimize processes and troubleshoot operational issues in a regulated manufacturing setting. You will apply basic engineering principles to design and implement system modifications and to organize and present results for projects of minor scope and complexity.

The role requires experience with GMP, GDP, change control, and lifecycle management, with the ability to coordinate cross‑functional teams and document technical work accurately.

Qualifications

• Experience troubleshooting equipment/process in regulated environments.
• GMP knowledge and familiarity with GDP documentation practices.
• Experience with change control and risk assessments.
• Ability to coordinate cross-functional teams and stakeholders.
• Experience supporting equipment decommissioning and lifecycle management.

Responsibilities

• Provide solutions to technical problems of moderate scope in manufacturing.
• Act as technical expert during troubleshooting and cross-functional discussions.
• Supervise manufacturing processes for performance indicators and mentor junior staff.
• Collaborate with manufacturing, maintenance, quality, and validation on modifications.
• Support deviations, equipment qualification, process validation, and training activities.
• Apply engineering principles to design and implement system modifications.
• Organize and present results for operational issues or projects of moderate scope.
• Support 7/24 non-standard shift operations as needed.

Skills

Process troubleshooting

Regulated environments

GDP knowledge

Change control

Documentation management

Regulatory compliance

Cross-functional coordination

Project management

Qualification & validation

Education

Masters in Engineering

Bachelor’s in Engineering

Job description

Inteldot is seeking an engineering professional to optimize processes and troubleshoot operational issues in a regulated manufacturing setting. You will apply basic engineering principles to design and implement system modifications and to organize and present results for projects of minor scope and complexity.

The role requires experience with GMP, GDP, change control, and lifecycle management, with the ability to coordinate cross‑functional teams and document technical work accurately.