Drive problem solving for key packaging quality issues using 8D/Drill Deep & Wide
Develop & execute quality tools, processes, projects with influencing engineering & manufacturing plants quality teams to improve product quality
Deliver significant improvements to the bottom line through Product Damage improvement
Plans and conducts document, internal and external GCP audits of clinical research activities to assess compliance with FDA, ICH GCP, and local regulations, with protocol and company SOPs
Audits and evaluates service providers
Evaluates corrective and preventative action responses to audit findings for adequacy and timeliness and manages the closeout of all corrective and preventative actions
Develops audit plans for Acorda clinical studies
Sr.
✓Manager Quality: BE/ M. Tech Mech, must able to handle team of 6( two plants) , Experience required: 10 years
Key Skills & Technical Requirements
SR. Manager Quality
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