Validation Associate

SmartRecruiters, Inc.; Rocky Mount (NC); On-site; USD 52,000 - 74,000; Full time

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 a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

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

must
be able to Lift and carry light loads as necessary in conducting
testing, sitting, standing, walking, weekend or long hours based on
testing schedule, wear proper gowning and PPE in manufacturing areas as
required to meeting GMP and OSHA requirements.

• 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.

Additional Information

$46hr

12 MONTHS