Ad copy

Application Deadline: Wednesday July 16th. Learn Commissioning & Qualification of Equipment and Systems and Populate an IQ OQ PQ Equipment Validation Protocol. https://www.getreskilled.com/iq-oq-pq/ - Validate equipment. - Leran to excute an IQ OQ PQ Validation Protocol. - Validate Equipments & Systems. - Read P&IDs & Piping Isometrics. - Join a Validation or Qualification Team in Just 4 Months Build on your industry experience and start a higher-paying career in validation. Turn your practical work experience into an advanced certification Enroll in this program to learn: How to prioritize which parts of the equipment system are critical to validate and which parts are not etc, using component impact assessments and risk management tools. How to read/interpret the engineering documentation such as P&IDs, Piping Isometrics & Electrical Loop Drawings used to define the equipment system. How the intent of a process (like maintaining the product at the required temperature) is linked to the equipment that will be used to do this. The tests along with the functional test scripts necessary to confirm that the installed equipment is fit-for-purpose, i.e. that it will do what it states that it will do based on the User Requirement Specifications). How to use a traceability matrix tool to ensure that all requirements defined within the User Requirement Specifications (URS) are tested in the protocol. How to qualify equipment, instruments and piping systems, and automation controls. How to document all of these steps in a validation protocol which you will develop as your end of module assignment. You’ll produce your own 120-page plus IQ OQ PQ Validation Protocol to commission and qualify a clean-in-place system The protocol will detail the following elements; Product characteristics – showing what your system is looking to achieve/produce Production equipment – detailing the equipment necessary Test scripts and methods – telling you the steps involved in conducting a test Test parameters and acceptance criteria – defining acceptable test results Test checksheets – documenting and recording the test results Final approval – documenting that the validation process has been successfully carried out There are 2 modules in this 15-week program Module 1 – Manufacturing Safe Medicines (Weeks 1-5) In this module, you’ll learn about the systems used in pharmaceutical manufacturing. You’ll learn about the rules and regulations that need to be followed. And you’ll learn enough technical information to get you talking to employers. Module 2 – Commissioning and Qualification (IQ OQ PQ) of Equipment and Systems (Weeks 6-15) This is the validation bit. In this module, you will develop your own 100-page Validation Protocol to commission and qualify a clean-in-place system. You will also learn to read P&IDs, Piping Isometrics & Electrical Loop Drawings used to Develop Validation protocols. And you’ll learn how to qualify equipment, instruments, and piping systems, along with automation controls and building facilities.th