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The Clinical Laboratory Scientist(CLS) is responsible for performing medium and high complexity laboratory testing on patient specimens, performing quality control and quality assurance procedures and complying with all applicable local, state and federal laboratory requirements.
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Ability to balance generating high quality data within the limitations of a high-throughput environment. Hands-on experience with one or more current LC-MS/MS platforms (e.g., Sciex Triple Quads, Agilent HPLCs, Shimadzu HPLCs, LEAP autosamplers, ADDA) and software (e.g., Analyst, Discovery Quant, Leadscape, Electronic Laboratory Notebook.
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Immediate opportunity for an Environmental Health & Safety Specialist II to work with multi-national pharmaceutical company dedicated to pharmaceutical research and vaccine development. Certification/ or willingness to obtain: CHMM (Certified Hazardous Materials Manager) or RCRA (Resource Conservation and Recovery Act) Training (Strongly preferred.
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Understand the quality requirement of biologics drugs application, cooperate with the application to the complete the experiments or reports. Perform routine analytical tests (e.g., SEC, CE, ICIEF, Protein A) to support the upstream and downstream process development.
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MedRhythms is looking for a Quality Assurance Specialist to ensure that our revolutionary medical technology is up to the highest standards of safety, security, and quality.
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A leading Defense and Space Manufacturing Company is seeking a Quality Assurance Specialist to join their team in Pearl Harbor, Hawaii. Knowledgeable in shipyard, maritime, and commercial work practices, quality assurance, safety, metal-work and contracting methods.
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The Quality Manager collaborates closely with cross-functional teams, including Chemistry, Manufacturing, and Controls (CMC), Regulatory Affairs, and Quality Assurance and Vistagen's GMP suppliers, to drive continuous improvement initiatives and maintain a culture of quality excellence.
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The Quality Assurance Technician will perform various assignments with direction including, but not limited to, quality audits; developing and maintaining databases; and collecting, analyzing and communicating data of varying complexity to departments across the organization.
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Minimum experience required of the position Four years of nuclear power plant experience in the field of quality assurance or supervisory experience in plant operations. Requires minimum one year of experience in the overall implementation of the Quality Assurance Program and ANSI/ANS N45.2.
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Position Summary The Quality Assurance Support Specialist attends to requests of the Director of Quality Assurance when assistance is needed, including performing confidential administrative duties for the company.
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Internal and External Contacts: QC Biological & Analytical Sciences, Quality Assurance, Validation Vendor: Waters Customer: Analytical Development, Process Development, Manufacturing, Supply Chain.
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Develop, lead, direct, update, reassessment, verification and periodic validation of FSQA programs including HACCP Program, Sanitation Standard Operating Procedures, Pest Control, Good Manufacturing Practices, Approved Supplier Program, Foreign Material Control, Plant Sanitation, Chemical Control, Product Quality Assurance, FSQA Customer Complaints, Food Defense and Security.
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As a Senior Quality Assurance Specialist, you will be responsible for maximizing crew quality performance within the Spartanburg Site. In this role, you will be expected to have an in depth understanding of the input variables and measurement systems in our production equipment, and their impact on final product quality.
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The Compliance Quality Assurance Specialist works under the Quality Assurance Officer as well as with the Financial Intelligence Unit (FIU) Investigations Director, the Deputy OFAC Officer, and the Head of the Customer Intelligence Unit (CIU.
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Responsible for working as the Quality Assurance member on new product development projects for the B. Braun Medical Inc medical device franchise. Provides Design Assurance Quality Engineering support, to the R&D organization for new products, design modifications, and OEM customers; this includes creation of Quality and Validation plans, risk analysis, traceability matrixes, URS/FS, Design Reviews, customer interface, and follow through.
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Title: quality assurance specialist Company: Randstad Life Sciences Us
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