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Maintains the Quality Assurance (QA) training program, document control, customer complaint program and CAPA program. Quality Assurance Specialist. Manages the review cycle of QA controlled documents to assure practices reflect written procedures.
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Document control, archive, archival, archivist, doc control, qa, quality assurance, quality associate, quality specialist, quality assurance specialist, gmp, cgmp, gxp, mastercontrol, veeva vault, edms, document management system, pharma, biopharma, medical device, biotech, biotechnology, fda, quality systems, qms, eqms, clinical manufacturing, commercial manufacturing, novel pharmaceutical, novel drug, novel therapeutic.
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Provides professional accounting and financial specialist support to a project team, reviewing and evaluating project charges for accuracy, completing cost transfers, establishing and updating funding as needed, instituting and maintaining project budgets, and ensuring that all project data is current.
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The Quality Assurance Floor Support Specialist works as a member of the QA Floor Support team and reports to the QA Parenteral Associate Director. QA Floor Support Specialist oversees visual inspection production functions to achieve patient safety and site goals through effective quality oversight.
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The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various. Understanding and familiarity with FDA and European regulatory requirements, guidelines.
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Applies 5 Pillar Quality standards in accordance to Truly Green QA Model. Occasionally assists with inbound customer service calls based on business needs. Applies 5 Pillar Quality standards in accordance to Truly Green QA Model.
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QA Document Control Specialist (Part Time) Our client, a global leader in biotechnology and innovation of therapies for rare and genetic diseases and life-threatening conditions is seeking a QA Documentation Control Specialist II that will be responsible for responsible for the maintenance of the cGMP controlled documentation system.
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Innova Solutions is immediately hiring for a Quality Assurance Specialist - 3r d Shift. Perform QA in-process inspections for each department/line once per shift by checking the following: production paperwork, retain sample, code date/lot number/best by date, weight check documentation, metal detection documentation, label, color code, department cleanliness employee GMP practice and checking for any potential allergen cross-contamination.
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The salary range for a QA Specialist (Customer Service) is $65,000 - 75,000 and will be eligible for equity and an annual performance-based bonus. 2-4 years of QA and customer support experience.
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Monitors Licensing Specialist/Recruiter progress in licensing homes and recruitment plans. Implements QA requirements as directed by State Compliance Director. Supervises the Licensing Compliance Specialist.
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The QA Specialist is responsible for monitoring products and employee practices on the manufacturing floor to insure the safety and quality of products manufactured by Georgia Nut Company.
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Click on Apply Now to be considered for this Quality Assurance Specialist job in Rockford, IL.Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan.
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Prior experience in a GMP quality (Manufacturing/QA/QC) environment, experience in drug substance, drug product and final packaged product a plus. The Quality Specialist provides support for the business' product development portfolio and ensures adherence to CGMP compliance in a regulated environment.
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Piper Companies is searching for an experienced GCP QA Professional to join a global biopharmaceutical company producing therapies for neurology and rare disease disorders as Senior Quality Assurance (GCP) Specialist.
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The Quality Technician I is responsible for supporting the business with QA activities to ensure nonconforming products are not produced and shipped to customers. The Quality Technician I is responsible for supporting the business with QA activities to ensure nonconforming products are not produced and shipped to customers.
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