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General Scope of Work: This position will oversee of all aspects of the company's quality improvement efforts. Will plan and direct quality assurance policies, programs, initiatives, strategic plans and resources that are required to meet the expectations of both internal and external customers. CAPA, Supplier Audit, Internal Audit, Product Release, Document Control, Training, Change Control and Management Review. Procurement and assignment of Quality Assurance Resources. Critical review and reporting of Quality Assurance output and performance. Budget, management and reporting of Quality Assurance expenses. Coordination, facilitation and review of validations required in support of Product and Manufacturing Engineering projects.

Require: BS/BA in Mechanical Engineering, Manufacturing Engineering, Science or Business Administration.10+ years experience in QA systems implementation and management with 5 years as a CQE/CQM ideally in a medium-size pharma manufacturing environment.

E-mail resume to: smorley@themorleygroup.com

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