Validation Associate

Job Description

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.

Validation Associate duties:

• 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