United Pharma, a leading pharmaceutical company committed to quality and innovation, is actively seeking a skilled Validation Engineer to join our team in Indianapolis, Indiana. This role is critical in supporting large HVAC building automation systems within FDA-regulated pharmaceutical environments to ensure compliance with safety and regulatory standards.
If you have experience working in regulated environments and a passion for maintaining high standards in pharmaceutical manufacturing, this opportunity is perfect for you.
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Key Responsibilities
- Support large HVAC building automation customers ensuring seamless system performance.
- Execute CQV (Commissioning, Qualification, Validation) protocols including IQ, OQ, and PQ steps.
- Work closely within FDA-regulated environments ensuring regulatory compliance and human safety.
- Maintain and document validation activities aligned with industry best practices.
Skills & Experience Required
- Experience in regulated environments such as FDA, GMP, or equivalent compliance frameworks.
- Strong knowledge of CQV, IQ, OQ, PQ validation processes and documentation.
- Deep understanding of safety-critical systems in pharmaceutical manufacturing.
- Ability to navigate complex compliance requirements and execute validation protocols efficiently.
Why Join United Pharma?
- Opportunity to work in a cutting-edge, FDA-regulated pharmaceutical environment.
- Collaborate with a passionate team dedicated to quality and regulatory excellence.
- Grow your career with a company focused on innovation and compliance.
- Competitive salary and growth prospects in a stable industry.
Location
Indianapolis, Indiana, USA
How to Apply
Interested candidates should send their updated resume to bindu@unitedpharma.us to apply for this position.
