What are the responsibilities and job description for the Mid-Level Validation Engineer position at United Pharma Technologies Inc?
Job Title: Mid-Level Validation Engineer
Location: Boulder, Colorado
Position Overview:
We are seeking two Mid-Level Validation Engineers to join an on-site team in Boulder, CO, supporting the qualification of legacy equipment to Operational Qualification (OQ) status. This is a hands-on role focused on executing validation protocols and generating documentation in a fast-paced, regulated environment.
Key Responsibilities:
- Execute Installation Qualification (IQ) activities
- Develop and maintain validation documentation in accordance with internal protocols
- Support qualification of legacy API equipment, including:
- Reactors
- Vessels
- Custom baths
- ANFDs (Agitated Nutsche Filter Dryers)
- Simple filters
- Ensure compliance with GMP standards and validation protocols
- Collaborate with site teams to meet project timelines and deliverables
Required Qualifications:
- 5 years of experience in equipment validation, preferably in an API manufacturing environment
- Strong understanding of IQ/OQ/PQ validation principles
- Ability to work independently and deliver under tight timelines
- Excellent attention to detail and documentation practices
- Must be available 100% onsite in Boulder, CO
