Process Development Scientist - Formulation and Aseptic Filling

BioPharma Consulting JAD Group; Juncos (PR); Presencial; USD 85.000 - 110.000; Jornada completa

Descripción de la vacante

BioPharma Consulting JAD Group is seeking a Process Development Scientist to design, execute, and interpret studies that support formulation and filling processes at a leading biotech site in Juncos, Puerto Rico. The role requires monitoring process data to assess product impact and providing manufacturing floor support for 24/7 operations.

The candidate should have Doctorate or Master’s with experience or a Bachelor’s with extensive scientific experience, with strong writing skills and cGMP

Formación

• 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).

Responsabilidades

• 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.

Conocimientos

Biopharma manufacturing

Formulation science

Aseptic filling

Process monitoring

Data trending

JMP

Educación

Doctorate

Master’s + 2 years experience

Bachelor’s + 4 years experience

Herramientas

JMP

Descripción del empleo

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