Senior Validation Engineer

Job Location Compli, LLC, a George Butler Associates' affiliate, was founded in 2001 to provide commissioning, validation and regulatory support services to the life sciences industry. Efforts consist of providing commissioning, qualification and validation project deliverables to clients around Lifecycle validation efforts. This included, but is not limited to, developing Lifecycle documentation (URS's, Trace Matrices, System/Component Impact Assessments, Risk Assessments, Master Planning, etc.), developing Commissioning, Qualification and Validation documentation (CQV protocols, executing protocols, developing summary reports and final report packages). Collate and analyze data and prepare Summary Reports. Perform all other tasks, and projects. Other duties as assigned. Preferred prior experience in performing CQV services on the following systems / equipment: Utilities including HVAC systems and Purified Water / Water for Injection Systems Lyophilizers / Freeze Dryers Spray Dryers Aseptic Fill Lines and associated equipment Blending Equipment BS in science related field (e.g., engineering, biology, microbiology, chemistry, etc.). Minimum 5+ years' experience specific to commissioning, qualification and validation activities. Prior experience in the pharmaceutical / biotech manufacturing industry. Prior experience with Current Good Manufacturing Practices and other relevant regulations related to the Pharmaceutical / Biotech industry. Must have strong interpersonal and communication skills. Must have strong critical thinking skills. Travel Compensation It's more than just a job... To view full details and how to apply, please login or create a Job Seeker account