Validation Engineer - Houston, TX
Unicon Pharma Inc
Job Title: Validation Engineer II
Shift Timings: Monday - Friday 5x onsite 1st shift
Summary:
- Develop and execute validation protocols and reports for equipment, utilities, and facilities (e.g., IQ, OQ, PQ).
- Develop and execute CQV deliverables for Temperature Mapping (Controlled Temperature Units).
- Coordinate validation activities with cross-functional teams including Manufacturing, Quality Assurance, Engineering, and R&D.
- Analyze validation data, identify deviations, and recommend corrective and preventive actions (CAPAs).
- Prepare and present validation summaries and reports to internal and external auditors.
- Participate in the review and approval of change controls related to validated systems.
What we are looking for:
- Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or equivalent) or a related scientific discipline.
- Minimum of 2-6 years of experience in validation within the biopharmaceutical or pharmaceutical industry.
- In-depth knowledge of cGMP, ICH guidelines, FDA regulations (21 CFR Parts 210, 211, 820), and other relevant regulatory requirements.
- Ideal candidates will have hands-on experience in temperature mapping for Controlled Temperature Units and familiarity with FDA and cGMP standards. Proven experience IQ, OQ, PQ.
Vacancy posted more than 2 months ago
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