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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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The Senior Director, Quality Assurance is responsible for ensuring adequate quality assurance activities within all GXP areas at QurAlis Corporation. This individual will work closely with CMOs, CMC, Regulatory, Clinical, Quality Systems, Validation and Supply Chain Operations teams to maintain drug product supply.
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The Senior Director, GCP Quality Assurance coordinates GCP Compliance activities with Clinical Operations, Regulatory Affairs, Clinical Supply & Logistics, Sample Management and Pharmacovigilance as well as vendors supporting Scholar Rock sponsored Clinical Studies.
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Quality Assurance, Associate Software Engineer in Test page is loaded. Play a major role to improve quality, functionality, reliability and usability of software products. Learn quality and coding best practices and standards, and train teams on best quality practices.
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Must have strong knowledge of biologics and small molecules manufacturing, materials management, quality control, quality assurance and CMC regulatory requirements. The position is responsible for product development, technology transfer and overall management of CMC activities related to ensuring robust development and reliable GMP supply of oligonucleotide conjugates and intermediates.
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Reporting to the Assistant Clinical Director (ACD) of X-Ray, the Quality Assurance (QA) Specialist facilitates the X-Ray QA program and provides appropriate education and guidance to staff which includes assessing, planning, implementing, and evaluating both orientation and continuing education programs to enhance the quality of patient care services.
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Responsible for Quality & Controls Assurance programs, activities and reviews, including claims reviews; call center and digital communications reviews; Medicare Risk Adjustment, HCC, clinical and coding reviews; DRG and medical records reviews; technology/systems and coding upgrade and implementation reviews (e.g. final user acceptance testing, etc.
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The Salesforce QA Lead will be responsible for the end-to-end development and support of a detailed Quality Assurance plan (QA Plan) optimized to reduce and eliminate any existing security or privacy vulnerabilities in the Salesforce-based licensing system.
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The Senior Analyst / Scientist will work cross-functionally with others in Quality Control, Analytical Development teams, Quality Assurance, and Manufacturing, as needed. The individual will also work on data trending, invalid assays investigations, quality events (investigations, deviations, Change control, CAPAs) and analytical assays for AAV efficacy (potency), safety and product quality.
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Requirements:BS in a scientific discipline with 8 years’ experience in pharmaceutical / biotech industry within Quality Control or Quality Assurance, at least 4 years managing QC Testing LaboratoryExperience with raw material testing programs and methodologies (FT-IR, Raman, NIR, Dot-blot, ELISA, and HPLC)Ability to communicate and work independently with scientific/technical personnel.
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The Director, GMP Quality Assurance will lead the GMP quality function by supporting and providing oversight of CMC activities, establish and manage GMP quality systems, and ensure GMP compliance.
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You'll be responsible for the operation and quality assurance of film processing, patient monitoring, and x-ray equipment. Job Description & Requirements Specialty: Interventional Radiology Technologist Discipline: Allied Health Professional Start Date: 06/24/2024 Duration: 13 weeks Employment Type: Travel Setting: Hospital Join our compassionate team of Imaging Professionals as an Interventional Radiology Tech and use your expertise to perform invasive diagnostic and interventional procedures at a reputable heatlhcare facility currently experiencing a staffing shortage.
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The QA Analyst will spearhead Quality Assurance tasks including test planning, coordination, testing, and defect tracking. We are in search of self-motivated, critical-thinking individual with a passion for Quality to join our Student Information Systems applications support team as a Quality Assurance Analyst.
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Professionals in QRM will work with the Americas Consulting Quality (ACQ) Assurance Monitoring and Inspections (M&I) Program leader and team to assist with Assurance-related external and internal inspection activities.
$136,100 - $311,000 a yearFull-timeExpandUpdated 12 days ago - UpvoteDownvoteShare Job
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Monitors and tracks the quality of all statistical and statistical programming deliverables ensuring audit practices have been enacted to validate the quality and assurance of statistical content and supporting documents.
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quality assurance jobs in Boston, MA
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