Job Title: Associate Scientist II / Stability Coordinator

Location: Onsite – Puerto Rico

Schedule: Monday to Friday | 8:00 AM – 4:00 PM

Contract Type: 6-Month Contract (Temp-to-Hire) through ProQuality Network

🔬 Position Overview

Our client is seeking an Associate Scientist II / Stability Coordinator to support stability program activities within a cGMP-regulated environment. This role involves documentation management, stability study coordination, and technical review activities, requiring strong organization, attention to detail, and the ability to manage multiple priorities effectively.

📊 Key Responsibilities

• Manage and track documentation flow, including spreadsheets, reports, protocols, and stability data
• Author and support documentation such as:
• Stability protocols
• Technical reports
• Certificates of Analysis (CoA)
• Standard Operating Procedures (SOPs)
• Perform parallel and technical review of documents to ensure accuracy, completeness, and regulatory compliance
• Develop and execute stability work plans and schedules aligned with customer milestones and site metrics
• Ensure all activities are performed in compliance with cGMP standards
• Identify and support continuous improvement initiatives within stability and documentation processes
• Maintain organized records and ensure audit readiness at all times
• Comply with Environmental Health & Safety (EHS) requirements
• Perform additional duties as assigned

🎓 Qualifications

• Education: Bachelor’s degree in Life Sciences or Physical Sciences (e.g., Biology, Chemistry, Biochemistry)
• Experience: Entry-level role; no prior experience required

🧠 Skills & Competencies

• Strong proficiency in Microsoft Office (Word, Excel, Outlook)
• Ability to generate and maintain high-quality documentation in compliance with regulatory standards and SOPs
• Strong organizational, time management, and multitasking skills
• Ability to interpret technical instructions in written, oral, or diagram formats
• Solid mathematical and scientific reasoning skills
• Excellent written and verbal communication skills
• Ability to work effectively under pressure and meet deadlines
• Proactive mindset with strong problem-solving and critical thinking abilities
• Ability to quickly learn and retain technical information

💡 This is an excellent opportunity to build experience in stability programs, documentation, and regulatory compliance within a GMP environment, with strong potential for long-term growth.

📩 Interested candidates are encouraged to apply through the job description link with an updated resume to be considered for this opportunity.