Senior Engineer — Data, Automation & Validation

Integrated Services for Productivity & Validation, Inc; Juncos (PR); Sur place; USD 80 000 - 110 000; Plein temps

Résumé du poste

Integrated Services For Productivity & Validation, Inc in Juncos, Puerto Rico is seeking an engineering-focused professional to advance data analytics, dashboards, and validation documentation in a contract setting.

The ideal candidate has strong experience with data analysis, dashboard development, and enabling digital tools to address operational challenges in Drug Product manufacturing. Familiarity with GMP and PPQ processes is a plus.

Qualifications

• Preferred qualifications include experience with data analysis, dashboard development, statistical evaluation, GMP documentation, validation principles, and process improvement.
• Working knowledge of AI-enabled or automation tools such as Python, Codex, Power Automate, SQL, or VBA.
• Experience supporting Drug Product manufacturing, characterization studies, engineering runs, PPQ, validation deliverables, or manufacturing readiness activities will be a plus.

Responsabilités

• Translate operational challenges into practical digital tools, dashboards, or sustainable process improvements.
• Develop data-driven dashboards and analytics to support manufacturing readiness.
• Collaborate with cross-functional teams to implement validation-related digital solutions.

Connaissances

Data analysis

Dashboard development

Statistical evaluation

GMP documentation

Validation principles

Process improvement

Digital tools

Formation

Doctorate

Master's degree

Bachelor's in Engineering

Outils

Python

Codex

Power Automate

SQL

VBA

Description du poste

Integrated Services For Productivity & Validation, Inc in Juncos, Puerto Rico is seeking an engineering-focused professional to advance data analytics, dashboards, and validation documentation in a contract setting.

The ideal candidate has strong experience with data analysis, dashboard development, and enabling digital tools to address operational challenges in Drug Product manufacturing. Familiarity with GMP and PPQ processes is a plus.