JOB DETAILS
Senior Engineer - Process Monitoring, CPV and Manufacturing Systems
CompanyBioPharma Consulting JAD Group
LocationJuncos
Work ModeOn Site
PostedNovember 11, 2026
About The Company
BioPharma Consulting JAD Group provides a complete portfolio of technical support and solutions for the FDA regulated industry. We deliver solutions with a flexible cost effective approach to meet your company’s needs. BPC JAD group is a company created to help our customers bridge the gap between their business strategy and results.
Our mission is to help our clients succeed by partnering with them and providing value added business solutions on the validation, engineering and compliance fields.
We will carry out our mission by creating a long-term partnership with our customers and provide reliable and cost effective technical solutions.
BPC JAD Group objective is to deliver reliable tailored solutions; from providing consultation to becoming part of your staff. We will develop customized frameworks to help our customers unlock the hidden value in their plants, facilities, equipment and people with an optimal integration of resources regulations and technology.
About the 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.
- 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).
- Contract: 7 months, with possible extension
- Shift: Administrative, Monday–Friday
Key Skills
Process MonitoringContinuous Process VerificationManufacturing SystemsData AnalysisChange ControlGxPGMPData IntegrityExcelJMPPower BISQLSmartsheetPower QueryPower AutomateTechnical Documentation
Categories
EngineeringManufacturingTechnologyScience & ResearchData & Analytics
Job Information
📋Core Responsibilities
The Senior Engineer will lead continuous process verification activities, including data review and trend identification for drug product operations. They will also configure and support manufacturing systems while coordinating controlled document and process changes.
📋Job Type
contractor
📊Experience Level
2-5
💼Company Size
37
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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