Biopharma Process Development Scientist - Formulation

Integrated Services for Productivity & Validation, Inc; Juncos (PR); On-site; USD 70,000 - 110,000; Part time

Job summary

Integrated Services For Productivity & Validation, Inc in Juncos, Puerto Rico seeks a Process Development Scientist to join our contract team. The role focuses on supporting formulation and aseptic filling in a fast-paced biopharmaceutical environment.

The candidate will analyze process data, support deviations and investigations, provide manufacturing floor support, and collaborate across functions. Spanish and English proficiency required, with strong technical writing for regulatory audits.

Qualifications

• Experience in a commercial biopharmaceutical manufacturing environment, supporting formulation and aseptic filling.
• Understanding of protein science, formulation and filling processes.
• Experience with process monitoring, data trending, and JMP for statistical analysis.
• Experience supporting deviations, investigations, root cause analysis, and product impact assessments.
• Ability to provide manufacturing floor support in a 24/7 operation.
• Bilingual proficiency in Spanish and English (written and verbal).
• Strong technical writing skills for regulatory audit documentation.
• Excellent communication, presentation, problem-solving, project management, and cross-functional collaboration.

Skills

Biopharma manufacturing

Protein science

Process monitoring

Data trending

Statistical analysis (JMP)

CAPA & investigations

Manufacturing floor support

Bilingual Spanish/English

Technical writing for audits

Cross-functional collaboration

Project management

Communication skills

Education

Doctorate in relevant field

Master’s degree + 2 years scientific experience

Bachelor’s degree + 4 years scientific experience

Job description

Integrated Services For Productivity & Validation, Inc in Juncos, Puerto Rico seeks a Process Development Scientist to join our contract team. The role focuses on supporting formulation and aseptic filling in a fast-paced biopharmaceutical environment.

The candidate will analyze process data, support deviations and investigations, provide manufacturing floor support, and collaborate across functions. Spanish and English proficiency required, with strong technical writing for regulatory audits.