Senior Engineer - Process Monitoring, CPV and Manufacturing Systems
BioPharma Consulting JAD Group
- Work arrangement
- On-site
- Job type
- Contract
- Occupation
- Engineering, Science & Manufacturing
- Location
- Juncos, Juncos, PR
- Compensation
- Not disclosed
- Apply by
- May 14, 2027
About this role
Support manufacturing process engineering, system configuration and continuous process verification for drug product operations at a leading biotechnology company in Juncos, Puerto Rico.
What you'll do
- Lead CPV activities: process data review, trend identification, periodic reports and escalation of performance issues.
- Configure and support manufacturing systems (DME, PLM, MMP/MPP management): gather requirements, implement and test changes, and document results.
- Coordinate controlled document and process changes through review, approval and implementation.
- Interpret manufacturing data to support investigations, troubleshooting and continuous improvement.
- Use digital tools to improve reporting, monitoring and workflows.
Requirements
- Bachelor's in Engineering + 4 years (or Master's + 2, or Doctorate); Chemical, Mechanical, Electrical, Industrial, Biomedical or related.
- Manufacturing support in a GxP/GMP environment.
- Change control, controlled documentation and data integrity.
- Strong Excel; JMP and/or Power BI.
- SQL, Smartsheet, Power Query or Power Automate (a plus).
- Fully bilingual (English/Spanish).
Benefits
- Contract: 7 months, with possible extension
- Shift: Administrative, Monday–Friday