Occupation:Laboratory Technician |
Location:Raritan, NJ |
Education Level:Bachelor |
Will Relocate:YES |
Description
Profile Self-motivated Research Scientist - Regulatory QA/QC with a strong commitment to integrity and follow- through in delivering results. An organized and flexible, team oriented leader with meticulous planning practices, and adept in managing multiple priorities and innovation projects simultaneously. Formulation in Oral Care and Personal Care products. Provide strategic and tactical plans supporting new product development to meet corporate objectives. Perform critical function as a technical support for Marketing, Quality, Microbiology, and in house Manufacturing. A perfectionist which suits my work as it requires constant precision, vigorous quality control and optimization. Accomplishments Participated and worked on a patent for SprinJene toothpaste. Developed and formulated SprinJene Fresh Boost and SprinJene White Boost toothpaste. Had the opportunity to work on different areas from R&D, Marketing/sales, Microbiology QC, Quality, and Production. Developed and implemented systems. Monitor Experience in manufacturing and formulating medical device for diagnostic. Perform synthesis and purification of oligonucleotides according to SOP's and cGMP. Follow laboratory compliance according to quality standards and regulations. and document all QC related production activities according to established SOP's SOI's and cGMP. Follow laboratory compliance and regulatory affairs. Worked in Product Development and Operation team to ensure product safety compliance and performance. Experience in oral care and personal care QA/QC microbiology marketing/sales and production. Strong attention to detail and project management skills. Handled fast paced work environment. Developed and implemented systems Monitor, CoA's, and SDS according to QA/QC regulations and cGMP. Oversees and supervise employees during production from start to finished product, R&D, Microbiology, Analytical QC test, and Quality documentations. Data gathering and analysis of the results in a report. and document all QC related production activities according to established SOP's SOI's and cGMP. Reviewed documents and performed QC test USP microbial limit testing for raw materials bulk and finished product micro analysis of water environment monitoring and gowning according to regulation. Supervised developed and implemented systems SOP's and SOI's according to quality standards. Reviewed documents and performed Bioburden testing Part-Time Preservative Efficacy Test (PET)

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