Bilingual Pharma Process Engineer (Spanish/English)

Mykelly

Juncos (PR)

On-site

USD 70,000 - 90,000

Full time

8 days ago

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Job summary

Kelly Science, Engineering, Technology & Telecom (SETT) in Puerto Rico seeks an Engineer to support process optimization and troubleshooting in pharma/biotech operations. The role focuses on manufacturing, pilot plant, or capital projects within an environment that follows cGMP guidelines.

Under supervision, you will apply engineering principles to design system modifications, run experiments, and present results.

Qualifications

  • Master’s degree in Engineering or Bachelor’s with 2 years of engineering experience.
  • Working knowledge of cGMP procedures in pharma/biotech production.
  • Experience supporting operation, troubleshooting, optimization of HVAC, utilities, and facility systems in regulated pharma/biotech.
  • Strong GDP knowledge.
  • Experience managing technical documentation and records.
  • Bilingual: Spanish and English.
  • Willingness to work non-standard shifts, including weekends and 12-hour shifts.

Responsibilities

  • Under general supervision, provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.
  • Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects.
  • Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity.

Skills

cGMP knowledge
pharma/biotech engineering practices
HVAC systems experience
GDP knowledge
technical documentation management
Bilingual: Spanish and English

Education

Master’s degree in Engineering
Bachelor’s degree in Engineering & 2 years of Engineering experience

Job description

Kelly Science, Engineering, Technology & Telecom (SETT) in Puerto Rico seeks an Engineer to support process optimization and troubleshooting in pharma/biotech operations. The role focuses on manufacturing, pilot plant, or capital projects within an environment that follows cGMP guidelines.

Under supervision, you will apply engineering principles to design system modifications, run experiments, and present results.

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