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Process Development Scientist (Biotechnology) 3220901

Process Development Scientist – Biotechnology Industry

Location: East Region, Puerto Rico (Open to Residents of Puerto Rico)

Work Schedule: Hybrid preferred onsite | Administrative Shift

Contract Type: By contract through ProQuality Network

Duration: Approximately 6 months

Open Positions: 1


Job Summary

ProQuality Network is currently seeking a Process Development Scientist for a contract position with our client in the biotechnology industry. This role is ideal for professionals with a strong scientific background and experience in experimental design, validation processes, and process development within the biotech sector. The selected candidate will play a vital role in the design, execution, and analysis of scientific experiments supporting ongoing and future projects.


Key Responsibilities

  • Conceive, design, implement, and execute scientific experiments under general guidance.
  • Develop and apply experimental strategies and assess the impact of data on project outcomes.
  • Ensure compliance with protocols, applicable guidelines, and regulatory standards.
  • Generate robust and reliable data to support new processes and process improvements.
  • Maintain expertise in scientific field, monitor technological developments, and apply relevant advancements.
  • Independently author technical reports, summary documents, and regulatory documentation.
  • Participate in cross-functional project teams and contribute to department-wide initiatives.
  • Support the execution and documentation of validation and equipment characterization processes.
  • Engage in scientific collaboration and mentoring opportunities.
  • Contribute to safety, recruitment, and committee functions as needed.


Preferred Qualifications

  • Strong knowledge of vision system technologies and inspection/packaging concepts.
  • Experience in:
  • Development and execution of processes/equipment characterization.
  • Establishing testing strategies and developing characterization protocols.
  • Supporting Site Acceptance Tests (SATs), document generation, and validation strategies.
  • Risk assessments and QRAES.
  • In-depth understanding of validation processes for new equipment installations.
  • Ability to resolve routine technical problems and offer innovative solutions.


Educational & Software Requirements

  • Doctorate degree, or
  • Master’s degree with at least 5 years of relevant scientific experience, or
  • Bachelor’s degree with at least 6 years of relevant scientific experience.
  • Proficient in Microsoft Office Suite: Word, Excel, PowerPoint.
  • Experience using data analysis tools preferred.


Core Competencies & Skills

  • Advanced scientific analysis, laboratory, and troubleshooting skills.
  • Strong verbal and written communication, including technical writing.
  • Project management, analytical problem solving, and creative experimental design.
  • Ability to lead, mentor, and collaborate across departments.
  • Strong organizational skills and ability to manage multiple projects.
  • Knowledge of cGMP, scientific protocols, and regulatory requirements.
  • Fully bilingual in English and Spanish.


If you are ready to grow your career in the biotechnology industry and make a meaninful impact, we invite you to apply through the job description link with an updated resume!


Thank you. We will be in contact soon.

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