Responsibilities: Develop and implement validation plans, protocols (IQ,OQ ,PQ), and reports for equipment, processes, and systems. Ensure validation activities comply with regulatory requirements, industry standards, and company policies. Develop test plans and acceptance criteria for validation activities. Work closely with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to coordinate validation activities. Qualifications : o Bachelor’s degree in Engineering, Life Sciences, or a related field. o Experience in validation within a regulated industry, such as pharmaceuticals, biotechnology, or medical devices. o Experience with Temperature and Steam Sterilization(Autoclave) o Experience in Equipment Qualification o Experience in validation protocols generation and execution o Flexibility to work weekends and extended hours as needed to meet project deadlines and support team efforts. o Strong organizational skills and attention to detail. o Pragmatic approach to validation processes, ensuring efficient and effective validation outcomes. Weil Group is proud to be an Equal Employment Opportunity Employer.
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Job Type
Full-time
Career Level
Mid Level