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Online Resumes with "Process development validation"
Scientist with broad-based experience in Diagnostics and Pharmaceutical R&D. Proven skills in Assay/Process Validation, PCR/RT-PCR/qPCR, Luminex Multiplex Technology and Virus Inactivation/Removal study. Experience in: Assay and Process Development/Optimization, Production Scale down, Microbiology/Virology, Molecular/Cellular Biology, cGMP/GLP/GDP, Troubleshooting
Versatile Research Assistant with 5+ years of experience in nanomedicine formulation, test methods process development and validation. Designing and executing studies to optimize the development process of new drug delivery methods/technologies, helping to ensure that products are ready for large scale manufacturing. Exceptional technology skills in the area of polymer characterization and tissue culture analysis. Proven ab...
Tags for this Online Resume: Synthetic organic chemistry, process development, validation, kilo lab, pilot plant, cGMP, DMF, drug design and develolpment, contract manufacturing, analytical chemistry, structure characterization, new molecules development
Qualifications Profile Highly accomplished engineer, with 19 years of industrial experience supported by 12 years of education in engineering. Extensive experience in product design, simulation, testing, and quality management systems. Experienced in hydraulic and controls components and systems (including hardware and software) design and applications. 14 years of experience using commercial CFD and FEA Software backed-by ...
SUMMARY OF QUALIFICATIONS * Over twenty years of experience managing regulatory affairs (RA)/quality assurance (QA), quality control (QC)/research & development (R&D) departments in pharmaceutical, medical device and dietary supplement manufacturing industries. Implemented Quality Management Systems meeting domestic and international regulatory requirements and ISO registration. Reviewed pre-clinical, clinical and pharmacok...
Summary: * Results-driven Manufacturing & Product Engineering Professional with a strong background in process development and validation, technology, product transfers, fixture design, development, and validation within highly regulated medical device environments including optical, opto-mechanical, and electro-mechanical systems and devices. * 10+ Years' Experience in writing validation/verification protocols and reports,...