Biopharma Process Engineer – On-site Juncos, PR

Biopharma-Consulting-Jad-Group; Juncos (PR); In loco; USD 85.000 - 110.000; Tempo pieno

Descrizione del lavoro

Biopharma-Consulting-Jad-Group is seeking an Engineer to provide engineering support for commercial operations at a biopharmaceutical manufacturing site in Juncos, Puerto Rico. The role focuses on process optimization, troubleshooting, and applying engineering principles to system modifications and capital projects.

Under general supervision, you will work with Manufacturing, Maintenance, Process Development, Utilities, Facilities, QA and Validation to develop requirements for system changes.

Competenze

• Master's degree in Engineering or Bachelor's degree in Engineering with 2 years of engineering experience.
• Experience in biotech/pharmaceutical industries is preferred.
• Familiarity with GMPs/GLPs and validation processes is desirable.

Mansioni

• Provide engineering support for commercial operations and process optimization at a biopharma site.
• Troubleshoot operational issues and apply engineering principles to system modifications and capital projects.
• Audit equipment performance and regulatory compliance; collaborate across departments to develop modification requirements.
• Support design, engineering, and construction projects within schedule and budget; assess quotes and cost estimates.
• Organize and present results for operational issues and engineering projects.

Conoscenze

Analytical problem solving

Technical report writing

Personal organization

Computer literacy

Bilingual English/Spanish

Formazione

Master's degree in Engineering

Bachelor's degree in Engineering + 2 years experience

Descrizione del lavoro

Biopharma-Consulting-Jad-Group is seeking an Engineer to provide engineering support for commercial operations at a biopharmaceutical manufacturing site in Juncos, Puerto Rico. The role focuses on process optimization, troubleshooting, and applying engineering principles to system modifications and capital projects.

Under general supervision, you will work with Manufacturing, Maintenance, Process Development, Utilities, Facilities, QA and Validation to develop requirements for system changes.