Description
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
• 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
Ready to Seal the Deal?
Submit your application today and take the next step in your career with Weil Group, Inc.
Apply for this Job