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Pharmaceutical Validation Professional

2 weeks ago

Jersey City, New Jersey, United States Piper Companies Full time
Job Title: Validation Engineer (CSV/CQV)

Piper Companies is seeking an experienced Validation Engineer (CSV/CQV) to work in Raritan, NJ. The ideal candidate will provide technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes while ensuring compliance with GMP and FDA standards.

Job Responsibilities
The Validation Engineer (CSV/CQV) will be responsible for conducting IQ, OQ, and PQ activities, validating new laboratory equipment and methods, supporting software updates, and creating SOPs, safety protocols, and work instructions. This role also involves overseeing site validation master plans, ensuring equipment and systems meet regulatory requirements, and driving continuous improvement initiatives.

Requirements
  • 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.
  • Skill in reviewing and approving validation protocols and reports for facility/equipment commissioning, qualification, and change management.

Benefits Package
  • Salary Range: $60-65/HR.
  • Long Term Contract.
  • Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays.