Quality Engineer Medical Device/Manufacturing Processes/GD&T in Indore, Madhya Pradesh for sale

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Quality Engineer
Medical Device/Manufacturing Processes/GD&T
Responsibilities
Work with internal partners and external supplier to remediate legacy PVE. Drive new or revised SPV special process validations as needed with specified suppliers. Support evaluating vendor risk during outsourcing activities.
Provide overall quality assurance leadership in the management of select contract manufacturing sites engaged in the production of Johnson and Johnson products. Provide complex product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes.
Utilize multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), and international organization for standardization (ISO). Report on contract manufacturer performance metrics.
Handle complex technical issues for manufacturing processes that are to be transferred to satellite facilities. Provide Quality Engineering support to suppliers including audits/assessments, inspection technique support, verification/validation activities, CAPA
Requirements
A minimum of a Bachelor's degree