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Breaking beauty boundaries is in our company's DNA. Since its game-changing launch of the first opaque nail enamel in 1932 (and later, the first long-wear foundation), Revlon has provided consumers with high-quality product innovation, performance, and sophisticated glamour.
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10+ Years experience in Quality Assurance function for TEXTILE products. Travels to domestic distribution facility in SC to train and manage QC staff to ensure that quality standards are understood.
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This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements.
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Our technologies included raw water pretreatment, degasification, hot lime softening, boiler make-up, condensate polishing, wastewater treatment, cooling, and oil/water separation for markets such as petrochemical/chemical, power generation and heavy industrial plants.
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Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position will ensure that all product, process or system related quality activities from raw material inspection through shipment of final product are in compliance with Corporate and governmental regulations.
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Experience with Veeva (Quality Docs, QMS and Training modules) a plus. Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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Position requires on-site presence at companies' HQ Essential Duties and Responsibilities Conducting Training: Developing and conducting training programs for personnel on GMP and GDP requirements, quality systems, and relevant procedures to ensure understanding and compliance throughout the organization.
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Contribute to vendor development and qualification efforts; audit vendors (e.g., raw materials, packaging, contract labs) to ensure cGMP compliance. A growing pharmaceutical organization is urgently hiring for a QA leader with extensive hands on experience with Quality Systems and Compliance.
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The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products. Experience in assay transfer, technology transfer, validation from Analytical Developmental group to Quality Control group.
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Position Brand Description: Conduct routine and nonroutine analyses of inprocess materials raw materials envroin sa alivate ys super r : deP go od duo ability sponseis yb as necaiet phemical acceptable GMP practices during of al work tasks.
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Pen/Pen Scripting, Python, UNIX/Linux, PL/SQL, Microservices, JIRA, Lean Kit, TDP, TOAD, SQL Developer, Rally, Selenium, Soap UI, Postman, XML, Quality Center, and Shell scripting. REQUIRES: Master’s or equivalent in Computer Science/Applications, Information Technology, Business Management/Administration or Electronics Engineering + 1 year experience as Software Quality Engineer, Software Quality Assurance Analyst, Test Engineer, Quality/Product Test Professional or related.
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Prepares monthly Manufacturing and Quality Related KPI’s. Proven quality and trustworthy performance have established widespread confidence in the HORIBA Brand. The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing, and metrology, to a broad range of scientific R&D and QC measurements.
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Performs raw material planning for projects within JDE. Monitor inventory levels for raw materials to ensure site meets inventory targets. Maintain effectiveness of the Quality System components relevant to this position.
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Candidate should have a good grasp of Quality Assurance and Engineering foundations and expertise across any of the major Industry domains such as Banking, Finance, Insurance and Healthcare. 15 - 18 years of experience in Software Quality Assurance & Testing, DevOps, Software engineering.
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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. Provide drug safety and pharmacovigilance leadership to the quality and compliance team, fostering a culture of collaboration, excellence, and continuous learning.
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raw job Title: quality in Piscataway, NJ
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