Sr. Quality Assurance Engineer with twenty years quality experience complying with FDA regulations. Energetic team player supporting quality within all manufacturing operations.
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Quality Engineer, CQA, Risk Management, Quality Systems , FDA, 21CFR Part 11
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Senor Director QA/QC/Validation, CAPA/Deviatios/Change Contrlol Systems extensive experience, Experience with US and EU regulatory agencies, including successful PAI, Established leadership and CMO and CRO management, Quality lead for local and global operations, Work experience in both GMP, GCP small and large companies
I am looking a professional growth.
Ideal Companies: I would like to work with Pharmaceuticals, Biotechnology, Medical Device or Chemical Industry.
Work as a quality engineer for medical device manufacture/ consultant or pharmaceuticals
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quality assurance, R&D, Biomedial, Medical Device , Cardiac Rythum
My objective is to support the goals of large and small Biotech/Pharmaceutical companies. Manage day to day operations, monitor activities, develop documents, set standards and lead cross functional teams to ensure quality standards, regulatory compliance and strategically move projects forward in the advance of human healthcare.
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Clinical, Trials, Project Managent, Quality, Regulatory, Managent
To advance and continuously improve professionally as a consultant engineer or manager with a manufacturer of high quality medical device products.
