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Validation Engineer
1 month ago
Responsibilities for the Validation Engineer (CSV/CQV)
- Provide technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes while ensuring compliance with GMP and FDA standards.
- Conduct IQ, OQ, and PQ activities, as well as validate new laboratory equipment and methods.
- Support software updates and assist in creating SOPs, safety protocols, and work instructions.
- Oversee site validation master plans, ensure equipment and systems meet regulatory requirements, and drive continuous improvement initiatives.
- Collaborate with internal teams and external partners to communicate project progress effectively.
- Bachelor's degree in Chemical Engineering, Biomedical Engineering, or a related field.
- Over 3 years of experience in biotechnology and/or pharmaceutical industries.
- Proficient in drafting SOPs, validation reports, and work instructions.
- Skilled in reviewing and approving validation protocols and reports for facility/equipment commissioning, qualification, and change management.
- Salary Range: $60-65/HR.
- Long Term Contract
- Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays
Keywords: Validation, CSV, CQV, IQ, OQ, PQ, Biomedical Engineering, Pharmaceutical, Biotechnology, Laboratory Equipment, Manufacturing Equipment, Equipment Validation, Equipment Commissioning, Validation Maintenance, Cleaning Validation,
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