Troubleshooting Engineer, GMP & Process Ops

Cis-International-LLC; Juncos (PR); On-site; USD 70,000 - 95,000; Full time

Job summary

Cis-International-LLC is seeking an Operations Engineer with a strong foundation in mechanical, electrical or chemical engineering to optimize processes and troubleshoot moderate-scale issues in pharma/biotech environments.

You will work under supervision, apply standard engineering methods, collaborate with cross-functional teams, and contribute to design, cost estimates, and implementation of improvements within GMP and regulated settings.

Qualifications

• Masters or Bachelor’s in engineering with 2 years of engineering experience.
• Educational background in Mechanical, Electrical and/or Chemical Engineering.
• Experience with equipment and/or process troubleshooting in a regulated environment.
• Knowledge of pharmaceutical/biotech processes and GMP production operations.
• Organizational & technical writing skills; strong English and Spanish communication.

Responsibilities

• Provide solutions to technical problems of moderate scope and complexity.
• Evaluate, select and apply standard engineering techniques under supervision.
• Perform routine technical tasks and contribute to cost estimates.
• Troubleshoot operations and coordinate with cross-functional teams for modifications.
• Design, engineering, and construction projects within schedule and budget constraints.

Skills

GMP knowledge

Bilingual English/Spanish

Technical writing

Presentation skills

Problem solving

Education

Masters or Bachelor\u2019s in engineering + 2 years experience

Mechanical, Electrical and/or Chemical Engineering

Experience in regulated environment

Pharma/biotech GMP knowledge

Job description

Cis-International-LLC is seeking an Operations Engineer with a strong foundation in mechanical, electrical or chemical engineering to optimize processes and troubleshoot moderate-scale issues in pharma/biotech environments.

You will work under supervision, apply standard engineering methods, collaborate with cross-functional teams, and contribute to design, cost estimates, and implementation of improvements within GMP and regulated settings.