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Process Development Scientist

Company: BioPharma Consulting JAD Group

Job Location: Juncos, Juncos, Puerto Rico

Job Type: CONTRACT - (ON_SITE)

Date Posted: April 17, 2025

External

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This individual will independently design, implement, and analyze scientific experiments to support the goals of the department and broader organization. The ideal candidate will bring strong scientific acumen, exceptional problem-solving skills, and experience with inspection development processes in a regulated environment.

Responsibilities:

  • Conceive, design, and execute scientific experiments with general guidance from supervisors.
  • Interpret experimental data and provide input to improve data reliability and robustness.
  • Ensure that all studies are compliant with protocols, cGMPs, and applicable regulatory guidelines.
  • Analyze and interpret data and assess its impact on current and future projects.
  • Monitor advancements in relevant scientific fields and introduce new methods or technologies as appropriate.
  • Develop and implement novel protocols to address project-specific challenges.
  • Independently author scientific reports, summaries, regulatory documents, and invention disclosures.
  • Participate in and potentially lead cross-functional project teams.
  • Mentor junior scientists and contribute to departmental initiatives (e.g., safety, recruiting).
  • Foster internal and external collaborations to support scientific innovation.
  • Utilize statistical tools (e.g., Minitab, JMP) for data analysis.
  • Maintain Good Documentation Practices and ensure compliance with quality standards.

Technical Skills & Competencies: 

  • Strong background in scientific theory and experimental design.
  • Proficient in statistical analysis tools (e.g., Minitab, JMP).
  • Advanced troubleshooting and analytical problem-solving skills.
  • Excellent verbal and written communication skills, including technical writing.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Fully bilingual (English/Spanish).
  • Strong knowledge of cGMPs, compliance standards, and documentation protocols.
  • Ability to work collaboratively across functions and manage multiple priorities.
  • Project management and time management skills.
  • Motivated team player with the ability to lead or supervise others when necessary.

Qualifications:

  •  Education: 
    • Doctorate degree, or
    • Master’s degree with at least 5 years of scientific experience, or
    • Bachelor’s degree with at least 6 years of scientific experience.
    •  Highly preferred: Degree in Engineering or related technical discipline.
  •  

Preferred Qualifications:

  • Experience with Inspection Development processes.
  • Proven track record of success in regulated environments.
  • Experience in developing scientific documentation, protocols, and reports.
  • Demonstrated excellence in teamwork, communication, and collaboration.
  • Administrative Shift (M-F)

I am not a product of my circumstances. I am a product of my decisions.

“Stephen Covey”
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