Lead Process Development Scientist - Sterile Manufacturing

Biopharma-Consulting-Jad-Group; Juncos (PR); On-site; USD 110,000 - 150,000; Part time

Job summary

Biopharma-Consulting-Jad-Group is seeking a Process Development Sr Scientist to independently conceive and execute experiments advancing process development, technology transfer, and sterile drug product operations. This role serves as a key scientific and technical resource, contributing to project leadership, data-driven decision-making, and continuous improvement of sterile drug product operations.

You will lead cross-functional teams, apply GMP principles, mentor staff, and contribute to

Qualifications

• Doctorate (PhD, PharmD, MD) with relevant postdoctoral experience where applicable or Master’s degree + 3 years of scientific experience or Bachelor’s degree + 5 years of scientific experience.
• Experience in sterile drug product manufacturing and aseptic processing.
• Strong writing and communication skills; GMP knowledge and data-driven decision making.

Responsibilities

• Independently design, execute, monitor, and interpret complex experiments to advance process development and manufacturing technologies.
• Prepare novel protocols and experimental designs addressing technical challenges and robustness.
• Lead data analysis to identify trends and support decision-making.
• Author technical reports, investigations, and change controls.
• Provide hands-on support to sterile drug product manufacturing including aseptic filling and process readiness.
• Support PPQ/validation, technology transfer, and continuous improvement initiatives.

Skills

Sterile manufacturing

Aseptic processing

Contamination control

Data analysis

JMP/Minitab

LIMS

Technical writing

Project management

Leadership

Bilingual English/Spanish

Education

PhD/PharmD/MD with postdoc

Master's +3 years

Bachelor's +5 years

Tools

JMP

Minitab

LIMS

HLEE

Job description

Biopharma-Consulting-Jad-Group is seeking a Process Development Sr Scientist to independently conceive and execute experiments advancing process development, technology transfer, and sterile drug product operations. This role serves as a key scientific and technical resource, contributing to project leadership, data-driven decision-making, and continuous improvement of sterile drug product operations.

You will lead cross-functional teams, apply GMP principles, mentor staff, and contribute to