Sr Engineer - 35710

Integrated Services for Productivity & Validation, Inc; Juncos (PR); On-site; USD 80,000 - 110,000; Full time

Job summary

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.

Responsibilities

• 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.

Skills

Data analysis

Dashboard development

Statistical evaluation

GMP documentation

Validation principles

Process improvement

Digital tools

Education

Doctorate

Master's degree

Bachelor's in Engineering

Tools

Python

Codex

Power Automate

SQL

VBA

Job description

Integrated Services For Productivity & Validation, Inc | Contract

Juncos, Puerto Rico

We provide the industry with a platform of solutions designed to their actual needs. We share and implement leading edge technology and methods that exceed customer expectation and deliver a one-stop provider of services focus on the well-being of the company and the employees.

Job Description

• Preferred qualifications include experience with data analysis, dashboard development, statistical evaluation, GMP documentation, validation principles, and process improvement.
  
• A standout candidate would have 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.
  
• The ideal candidate should be self-driven, comfortable working with ambiguous business needs, and able to translate operational challenges into practical digital tools, dashboards, or sustainable process improvements.
  

Requirements

• Doctorate OR Masters + 2 years of Engineering experience OR
  
• Bachelors in Engineering + 4 years of Engineering experience.