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buyer-in-ma
Mo goal, to become a certified as a Quality Auditor (CQA) with ASQ.
I hoping someone has recently done so and can share their knowledge such that enables to me focus me studies in a successful manor
About me?
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10+ Years GMP/GLP (R&D and Manufacturing, Clean Room Environments)
10+ Years Quality Systems (ISO, FDA, Military Specifications,
10+ Year Documentation (Standard Operating Procedures, Author and/or Revise)
8 Years Technical Writing (Process Flow, Job Aid’s, Operational Instruction)
8+ Years Records Management (Determine Life Cycle, Destruction Plan, Vendor Compliance)
8+ Years Process Mapping / Job Aid Creation (Visio, Corel, 3rd Party)
7 Years Engineering Change (BOM, Batch Records, Raw Materials..)
6+ Years AutoCAD / Solidworks
6 Years Research and Development Support
4 Years Equipment Changeover (GMP/GLP Equipment)
I hoping someone has recently done so and can share their knowledge such that enables to me focus me studies in a successful manor
About me?
\
10+ Years GMP/GLP (R&D and Manufacturing, Clean Room Environments)
10+ Years Quality Systems (ISO, FDA, Military Specifications,
10+ Year Documentation (Standard Operating Procedures, Author and/or Revise)
8 Years Technical Writing (Process Flow, Job Aid’s, Operational Instruction)
8+ Years Records Management (Determine Life Cycle, Destruction Plan, Vendor Compliance)
8+ Years Process Mapping / Job Aid Creation (Visio, Corel, 3rd Party)
7 Years Engineering Change (BOM, Batch Records, Raw Materials..)
6+ Years AutoCAD / Solidworks
6 Years Research and Development Support
4 Years Equipment Changeover (GMP/GLP Equipment)