Category / Type: Science & Biotechnology • Quality Assurance / Testing • Puerto Rico • Permanent / Full Time

support quality assurance programs, procedures, and controls while driving continuous improvement and ensuring compliance with applicable quality

• Monitor and track quality detractors through service and complaint databases.
• Ensure compliance with company policies, procedures, quality standards, and applicable safety and environmental regulations.
• Develop solutions to database issues of moderate scope and complexity.
• Write and support the development of Standard Operating Procedures (SOPs).
• Identify and analyze significant quality trends and report findings to management and cross-functional teams.
• Provide technical support in the use of information mapping technology.
• Support product review and release activities.
• Generate moderately complex statistical summaries and quality reports.
• Provide support for GMP auditing activities.

• Bachelor's Degree or equivalent.
• 2-4 years of relevant work experience.
• Experience in a Quality Assurance / pharmaceutical or regulated manufacturing environment preferred.
• Experience with investigations and complaints strongly preferred.
• Strong analytical, problem-solving, documentation, and communication skills.
• Ability to work effectively with cross-functional teams.