Our Central Life Sciences Quality Assurance team is searching for a Document Control and Auditing Specialist for our Dallas, TX facility. The ideal candidate will assist with all process auditing functions in order to assure all procedures and processes conform to the ISO-9001 standard, current Good Manufacturing Practice (cGMP) and current Good Laboratory Practice (cGLP) standards and regulations for EPA registered products. He/she will create, maintain and control critical quality product files and master manufacturing documentation for site manufacturing processes. He/she will also create, maintain and control standard operating procedures and work instructions for the Dallas site. This position serves as the official document controller and assists in
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