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.