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