The Role
Supports drug product manufacturing and process improvement through data analysis, dashboard development, statistical evaluation, GMP documentation, validation, automation, and digital tool development. The role translates ambiguous operational challenges into sustainable solutions and may support characterization studies, engineering runs, PPQ, validation deliverables, and manufacturing readiness activities.
Summary Generated by Built In
- 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.
Skills Required
- Doctorate in Engineering
- Master's degree in Engineering plus 2 years of Engineering experience
- Bachelor's degree in Engineering plus 4 years of Engineering experience
- Experience with data analysis, dashboard development, statistical evaluation, GMP documentation, validation principles, and process improvement
- Working knowledge of Python, Codex, Power Automate, SQL, or VBA
- Experience supporting drug product manufacturing, characterization studies, engineering runs, PPQ, validation deliverables, or manufacturing readiness activities
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The Company
What We Do
ISPV Inc. is a Life Science company that leads Productivity & Validation projects for the Pharmaceutical and Food industries.
