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Work with CSS leaders and Quality Assurance to unify processes and tools (where possible) to enable common ways of working between CSS and TT. Influence the continuous improvement of the product development process to ensure quality, robust development work products via metrics and design assurance processes.
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Collaborate with Quality Assurance, Quality Control, ADC Assembly, Packaging Engineering, NPD, and NPC in the collection of specifications, artwork, standards, etc. The Senior Specialist, Quality Assurance position is fully responsible for the support on pilot batching, scale up, line trials, up to first production of new product launches at a contract manufacturer (CM) of both Cosmetic and OTC products.
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Quality assurance check for each active study site for all regulatory documents, including: IRB Renewal, IRB Protocol Approval, Informed Consent Review, Signature of Co-Investigator, IRB Membership list, Lab Normal, CAP, CLIA, 1572 Form, Agreements, PI CVs.
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IT Audit Senior Manager - Project Assurance and Cybersecurity is an integral part of Internal Audit team and provides perspective on the assurance and advisory activities of strategic projects and delivers cybersecurity and infrastructure audits.
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Understands clinical trial operational complexities from study start up through enrollment, quality assurance, and study readout. Each leader is accountable to the therapeutic area, R&D, commercial, Company Leadership and the patients we serve for: (i) creating a vision and defining the strategy and integrated development plan for each asset within their portfolio, (ii) developing a set of objective criteria against which each asset advancing through the pipeline will be evaluated to enable debate and rapid, data-driven decision making; and (iii) ensuring that only high quality and differentiated assets enter the market.
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Identify requirements and ensure compliance with the many accrediting bodies and regulatory agencies dealing specifically with diagnostic imaging practices including quality assurance, infection control, patient safety, radiation safety, and OSHA.
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GCP, and GLP Quality Systems responsibilities include training, document management (SOPs and other controlled documents), change control, process improvement, and quality Quality systems activities will be coordinated with the Quality Systems group.
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Strong technical background in assay development, pharmaceutical analysis, bioassay, impurity testing, microbiology support, quality control, and stability management. Ph. D. or M.S in Biology, Chemistry, Micrology or related biotechnology discipline with a minimum of 15 years of Quality Control experience in biopharmaceutical or biotech industry.
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Demonstrated strong knowledge of ICH/GCP, regulatory guidelines/directives, clinical research processes and principles of Quality Assurance. Build and lead a Global Quality Strategy organization that provides experienced Quality Assurance support for Clinical Development projects and processes.
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The Chief Audit Officer (CAO) is responsible for providing independent assurance and consulting services that add value and improve operations. Certified Internal Auditor (CIA), Certified Public Accountant (CPA), Certified Risk Management Assurance (CRMA) or equivalent certification required.
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As a Quality Control Technician you'll be working to support the plant's day-to-day operations around quality. You'll be supported by your team with possibilities to grow into a Supply Chain Professional and directly impact the quality of our products - helping to improve real lives.
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We are adept in synthetic chemistry and process research services, which include Process Chemistry, Quality Control, Good Manufacturing Practice, Quality Assurance, Crystallization Research and Development, Solid Form and Polymorph Screening, Catalysis Screening and Enabling Technology, High Potent Compound Handling (HPAPI), Impurity Isolation and Structural Elucidation, and Preformulation and Formulation Research and Development.
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As a (Senior) Manager in External Data Quality Management, you will hold an important role within our Clinical Data Management team. (Senior) Manager, External Data Quality Management page is loaded.
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The Specialist, Quality Assurance provides Quality Assurance support for GMP Raw Materials that support the production of GMP Manufacturing operations of cell therapy products at our US Cell Therapy facility located in Princeton, NJ. Responsibilities include providing QA oversight of materials used for Manufacturing, Quality Control, and Process & Analytical Development.
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Our partnership with Rutgers University creates the state’s largest academic healthcare system dedicated to providing high-quality patient care, leading-edge research, and world-class health and medical education, further advancing our mission of providing high-quality healthcare in New Jersey.
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quality assurance jobs Title: quality assurance officer Company: Octapharma Plasma Inc in Cranbury, NJ
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