Pharma Process Engineer: GMP Troubleshooting & 24/7 Ops

PRPDG; Puerto Rico; On-site; USD 70,000 - 100,000; Full time

Job summary

PRPDG is seeking an engineering professional to optimize processes and troubleshoot operations in a regulated pharma environment. Under general supervision, you will apply basic engineering principles to design and implement system modifications for minor projects and proofs of concept.

The role requires a Bachelor’s or Master’s in engineering with 2+ years of experience in mechanical, electrical, or chemical disciplines, and proficiency in English and Spanish for cross-functional communication.

Qualifications

• 3+ years of engineering-related experience in mechanical, electrical, or chemical disciplines is advantageous.
• Experience in regulated environments and GMP production operations preferred.
• Strong written and verbal communication skills in English and Spanish.

Responsibilities

• Provide solutions to technical problems of moderate scope and complexity under general supervision.
• Evaluate and apply standard engineering techniques to design/modify systems or processes.
• Serve as technical expert during troubleshooting with multi-functional teams.
• Support manufacturing/quality systems such as deviations, equipment qualification, and process validation.
• Assist with 7/24 shift operations as needed.

Skills

Troubleshooting

Technical writing

Bilingual English/Spanish

Cross-functional collaboration

Education

Engineering degree (Bachelor's or Master's)

Job description

PRPDG is seeking an engineering professional to optimize processes and troubleshoot operations in a regulated pharma environment. Under general supervision, you will apply basic engineering principles to design and implement system modifications for minor projects and proofs of concept.

The role requires a Bachelor’s or Master’s in engineering with 2+ years of experience in mechanical, electrical, or chemical disciplines, and proficiency in English and Spanish for cross-functional communication.