CQV Validation Engineer

Job Title: CQV (Commissioning, Qualification, and Validation) Engineer Location: North Carolina, United States Job Description: We are seeking a highly motivated CQV Validation Engineer to join our team. The ideal candidate will be responsible for ensuring that systems, equipment, and processes meet all necessary validation standards. Core Skills: Strong knowledge of validation methodologies and processes Proficiency in developing and executing validation protocols Excellent problem-solving and analytical skills Attention to detail and strong organizational abilities Effective communication and teamwork skills Responsibilities: Develop and execute validation protocols for commissioning, qualification, and validation of equipment and processes. Collaborate with cross-functional teams to ensure compliance with industry regulations and company policies. Perform risk assessments and gap analyses for validation projects. Maintain validation documentation and ensure it is up to date. Participate in investigations and root cause analyses related to validation failures. Qualifications: Bachelor’s degree in Engineering, Life Sciences, or a related field. 2+ years of experience in CQV validation in the pharmaceutical or biotechnology industry. Strong understanding of regulatory requirements (FDA, EMA, etc.). Seniority Level: Mid-Senior level Employment Type: Contract Job Function: Validation Engineer Industries: Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research #J-18808-Ljbffr United Pharma Technologies Inc