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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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