Validation Engineer Jobs


Validation Engineer Jobs

Validation Engineers

Validation Engineer

Validation in the pharmaceutical and medical device industry is defined as the documented act of demonstrating that a procedure, process, and activity will consistently lead to the expected results. It often includes the qualification of systems and equipment. It is a requirement for Good Manufacturing Practices and other regulatory requirements. Since a wide variety of procedures, processes, and activities need to be validated, the field of validation is divided into a number of subsections including the following:

  • Cleaning Validation
  • Process Validation
  • Analytical Method Validation
  • Computer System Validation

Validation Engineer Recruitment Agency – JobContax Validation Design Engineer Jobs

JobContax specialises in the Global Recruitment of Validation Engineers. JobContax has over 10 years experience in the Validation Engineering Sector and has a worldwide network of contacts within the industry. JobContax has long standing partnerships with some of the world’s largest ECPM Contractors.

Validation Engineer Jobs Asia Validation Engineer Jobs Australia Validation Engineer Jobs Canada
Validation Engineer Jobs Ireland Validation Engineer Jobs UK Validation Engineer Jobs Middle East
Validation Engineer Jobs New Zealand Validation Engineer Jobs China Validation Engineer Jobs.

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Validation Process

OPQ Validation Process

OPQ Validation Process

The validation process consists of identifying and testing all aspects of a process that could affect the final test or product. Prior to the testing of a process, the system must be properly qualified. Qualification includes the following steps: (These steps are common practice for equipment (IQ, OQ and PQ).

  • Design Qualification (DQ)- Defines the functional and operational specification of the instrument, program, or equipment and details the rationale for choosing the supplier.
  • Installation Qualification (IQ) – Demonstrates that the process or equipment meets all specifications, is installed correctly, and all required components and documentation needed for continued operation are installed and in place.
  • Operational Qualification (OQ) – Demonstrates that all facets of the process or equipment are operating correctly.
  • Performance Qualification (PQ) – Demonstrates that the process or equipment performs as intended in a consistent manner over time.
  • Component Qualification (CQ) – Manufacturing of auxiliary components to ensure that they are manufactured to the correct design criteria.

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