Sterilization Validation Specialist

SmartRecruiters, Inc.

Rocky Mount (NC)

On-site

USD 52,000 - 74,000

Full time

2 days ago
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Job summary

Global Channel Management is seeking a Validation Associate to support sterilization validation activities in a manufacturing environment. The role involves coordinating protocol testing, data collection, and reporting results to ensure compliance with regulatory guidelines.

The candidate should have 3–5 years of experience in sterilization equipment processing, cycle development, process and validation engineering, and strong knowledge of cGMP regulations.

Qualifications

  • Validation Associate needs BS degree in a technical discipline.
  • Validation Associate requires:
  • Must have 3-5 years experience with Sterilization Equipment Processing.
  • A combination of Cycle Development; Process Engineering and Validation Engineering
  • cGMP regulations and latest validation guidelines
  • Able to work extended/odd hours around manufacturing schedule as required.
  • aseptic processing and terminal sterilization
  • strong project management.

Responsibilities

  • Ensure all aspects of validation adhere to required policies and procedures, including safety and training.
  • Writing and execution/coordination of validation protocol testing.
  • Compile and report on relevant validation data and generate summary reports to document the results of the validation studies.

Skills

Sterilization Equipment Processing
Cycle Development
Process Engineering
Validation Engineering
cGMP regulations

Education

BS degree in a technical discipline

Job description

Global Channel Management is seeking a Validation Associate to support sterilization validation activities in a manufacturing environment. The role involves coordinating protocol testing, data collection, and reporting results to ensure compliance with regulatory guidelines.

The candidate should have 3–5 years of experience in sterilization equipment processing, cycle development, process and validation engineering, and strong knowledge of cGMP regulations.

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