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Process Development Scientist (3147727)

Job Opportunity: Process Development Scientist (3147727)

📍 Location: Juncos, Puerto Rico (Open to Puerto Rico residents only)

🕐 Shift: 100% Onsite | Administrative Shift

📅 Duration: Approximately Seven (7) Months

🔹 Contract Opportunity through ProQuality Network


Summary:

ProQuality Network is seeking a Process Development Scientist to support our client, a leading organization in the pharmaceutical and biotechnology industry. This opportunity is offered on a contract basis and is ideal for professionals with a strong background in inspection development, statistical data analysis, and scientific documentation. The position is fully onsite in Juncos, Puerto Rico and requires hands-on scientific and project support under the guidance of senior leadership.


Key Responsibilities:

  • Conceive, design, implement, and execute scientific experiments aligned with project goals.
  • Analyze and interpret data, evaluate impact on projects, and communicate findings.
  • Ensure compliance with applicable guidelines, regulations, and study protocols.
  • Contribute to new processes by generating robust and reliable data.
  • Develop and implement experimental strategies and novel scientific protocols.
  • Collaborate with internal and external stakeholders to ensure scientific excellence.
  • Author technical reports, regulatory documents, and invention disclosures.
  • Participate in scientific forums, mentoring, safety committees, and departmental initiatives.
  • Maintain expertise in relevant scientific literature and evolving technologies.


Preferred Qualifications:

  • Experience with Inspection Development processes.
  • Basic knowledge in statistics using Minitab, JMP, or similar statistical software.
  • Strong project management skills.
  • Familiarity with the development of documentation protocols and technical reports.
  • Excellent communication and team collaboration abilities.
  • Knowledge and application of Good Documentation Practices (GDP).
  • Strong orientation toward quality, compliance, and continuous improvement.


Education & Experience Requirements:

  • Highly preferred: Educational background in Engineering.
  • Doctorate degree, or
  • Master’s degree with a minimum of 5 years of relevant scientific experience, or
  • Bachelor’s degree with at least 6 years of scientific experience.


Competencies & Skills:

  • Advanced scientific analysis and troubleshooting skills.
  • Expertise in laboratory practices and scientific theory application.
  • Strong understanding of cGMP regulations.
  • Proven ability to manage multiple projects and adapt to changing priorities.
  • Technical writing skills and regulatory documentation experience.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Bilingual: Fluent in English and Spanish (verbal and written).
  • Ability to lead, mentor, and collaborate across departments effectively.


📩 This is an excellent opportunity to make a meaningful contribution to pharmaceutical process development. If you're ready to bring your expertise to a high-impact project, we invite you to apply through the job description link with your updated resume.


Thank you. We will be in contact soon.

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