CQV Engineer

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Company: Katalyst HealthCares and Life Sciences

Location: Pennington, NJ 08534

Description:

Responsibilities:
  • Prepare commissioning, qualification, and validation documents for equipment, utilities, and systems.
  • Verify that systems and equipment operate according to design specifications and regulatory requirements.
  • Prepare and maintain comprehensive validation documentation, including test protocols, reports, and standard operating procedures.
  • Work closely with engineering, quality assurance, and production teams to resolve issues related to CQV.
  • Implement corrective actions and improvements to maintain compliance with regulatory standards.
  • Stay updated on industry regulations and standards related to CQV and ensure that all activities meet these requirements.
  • Conduct training sessions on CQV procedures and best practices for employees.
  • Participate in internal and external audits related to CQV activities.
Requirements:
  • Bachelor's degree in engineering, life sciences, or a related field.
  • Strong understanding of CQV protocols and regulatory requirements.
  • Excellent problem-solving skills and attention to detail.
  • Effective communication and teamwork abilities.
  • Relevant experience in the pharmaceutical or biotechnology industry is preferred.

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