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.