JOB DETAILS
Process Development Scientist - Formulation and Aseptic Filling
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 commercial formulation and aseptic filling operations at a leading biotechnology company in Juncos, Puerto Rico, as a process development scientist.
What you'll do
- Design, execute and interpret studies that support formulation and filling processes.
- Monitor and trend process data and assess product impact.
- Support deviations, investigations and root cause analysis.
- Provide manufacturing floor support for a 24/7 operation.
- Write technical reports and documentation ready for regulatory audits.
- Doctorate, or Master's + 2 years, or Bachelor's + 4 years of scientific experience (science or engineering).
- Commercial biopharmaceutical manufacturing, ideally formulation and aseptic filling.
- Protein science, formulation and filling processes.
- Process monitoring, data trending and statistical tools (e.g., JMP).
- Strong technical writing and cGMP knowledge; fully bilingual (English/Spanish).
- Contract: 12 months, with possible extension
- Shift: Administrative, 8:00 AM – 5:00 PM; may include 12-hour shifts, nights, weekends or holidays to support 24/7 operations
Key Skills
Process DevelopmentFormulationAseptic FillingBiotechnologyRoot Cause AnalysisTechnical WritingcGMPData TrendingStatistical ToolsJMPProtein ScienceRegulatory AuditsProcess MonitoringBiopharmaceutical Manufacturing
Categories
Science & ResearchManufacturingEngineering
Job Information
📋Core Responsibilities
The scientist will design and interpret studies to support commercial formulation and aseptic filling processes while monitoring process data. They will also provide manufacturing floor support, conduct root cause analysis, and prepare technical documentation for regulatory audits.
📋Job Type
contractor
📊Experience Level
2-5
💼Company Size
37
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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