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.*