Biopharma PD Scientist - Hybrid, 4-Month Contract

ProQuality Network

Juncos (PR)

Hybrid

USD 85,000 - 120,000

Full time

14 days+

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Job summary

ProQuality Network seeks a Process Development Scientist to support formulation and aseptic filling in a commercial biopharma manufacturing environment in Puerto Rico. The role designs, executes, and interprets experiments to improve processes and robustness, with cross-functional collaboration across manufacturing, quality, and engineering.

The position requires strong technical expertise in protein science, data analysis, and cGMP compliance, and bilingual English/Spanish communication for a

Qualifications

  • Experience in commercial biopharmaceutical manufacturing.
  • Fluency in English and Spanish (written and spoken).
  • Knowledge of cGMP and regulatory expectations.

Responsibilities

  • Design, execute, evaluate, and interpret scientific experiments to support process development initiatives.
  • Develop experimental strategies and provide technical recommendations to generate robust process data.
  • Ensure studies comply with approved protocols, cGMP, and regulatory guidelines.
  • Analyze and interpret data to assess project impact and support decision-making.
  • Support process monitoring, data trending, and statistical evaluations to identify improvements.
  • Provide technical support for deviations and investigations.

Skills

Biopharma processes
Data analysis
Troubleshooting
Cross-functional collaboration
Regulatory compliance

Education

Doctorate degree
Master’s degree +2 years
Bachelor’s degree +4 years

Tools

JMP

Job description

ProQuality Network seeks a Process Development Scientist to support formulation and aseptic filling in a commercial biopharma manufacturing environment in Puerto Rico. The role designs, executes, and interprets experiments to improve processes and robustness, with cross-functional collaboration across manufacturing, quality, and engineering.

The position requires strong technical expertise in protein science, data analysis, and cGMP compliance, and bilingual English/Spanish communication for a

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