Validation Engineer

In-depth knowledge of cGMP, ICH guidelines, FDA regulations (21 CFR Parts 210, 211, 820), and other relevant regulatory requirements. Coordinate validation activities with cross-functional teams including Manufacturing, Quality Assurance, Engineering, and R&D.

Role: Validation Engineer II
Location: 14905 Kirby Drive, Houston, TX - 77047
Contract length: 6+ months with potential for extension and/or permanent placement
Shift:Mon - Fri 5x onsite 1st shift
Pay Rate: $63/hour, based on experience + Weekly pay and healthcare benefits.

What you will do:

• 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:
• Bachelors 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.

#TMCA

•