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Reporting directly to the Senior Manager of Quality, this position collaborates closely with External Manufacturing Organizations (EMO), spanning pharmaceuticals, medical devices/combination products, consumer products/OTC, and biologics sectors, ensuring adherence to cGMP regulations and Bausch Health requirements.
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10+ years of experience in a GMP environment in pharmaceutical, biologics, vaccines, cell or gene therapy operations, including solid experience in Quality Systems and Regulatory CMC. Hands-on experience with designing and implementing GMP Quality Systems.
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Assist the Vice President Quality Assurance maintain a Reinsurance Claims Quality Assurance Program focused on assessing quality of technical claims handling, ensuring high quality claims handling for Everest, and identifying areas for improvement across the Global Reinsurance Claims Department.
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Reporting to the Executive Director of Development Quality Assurance, the Senior Director of Pharmacovigilance QA serves as a strategic partner managing quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and other related activities performed by Drug Safety & Pharmacovigilance and Medical/Clinical Departments.
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The Area Chief of Staff partners with the Practice Manager (if applicable) to drive the culture and delivery of quality care by the veterinary provider team (DVM, CVT, VA) in their assigned hospitals to ensure that every pet receives consistent care aligning with our six domains of quality(safe, effective, patient/client centered, timely, efficient and equitable care.
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10 years of Quality experience within Pharmaceuticals, OTC drugs, Dietary Supplements, Cosmetics, Foods and/or Medical Devices. Previous experience as Site Director or Site Quality Director.
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Being able to take good quality X-ray images following CityMD X-ray protocol in an efficient and accurate manner. Graduation from an accredited X-ray Technologist program. 4-6 months experience as a X-ray Technologist.
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Reporting to the Global Quality Engineering Director, the Supplier Quality Specialist will achieve ALAM goals in the areas of manufacturing quality, technology advancement, productivity, off-spec elimination, non-conformance elimination, customer satisfaction, and cost reduction.
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Use Mastercam CAD/CAM software to define efficient tooling operations to create high quality parts. The CNC Machinist Programmer will be responsible for operating several CNC machining tools to produce a variety of precision parts to support our growing sales of industrial drying equipment and systems.
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Maintain proper steam pressures, within specs, performing daily water treatment test, and water quality. Reports food safety and quality problems to Plant Management to initiate action.
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Job Description & Requirements Specialty: MRI Technologist Discipline: Allied Health Professional Start Date: 05/14/2024 Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel MedPro Healthcare Staffing , a Joint Commission-certified staffing agency, is seeking a quality MRI Tech for a contract with one of our top healthcare clients.
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As a private Independent practice, Luxottica operates the optical dispensary while the Affiliated Doctor operates the Doctors office and provides high quality optometric care and service to patients.
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Quality Lab Analyst+ Months RoleOnsite in Raritan, NJ.Full-Time, hybrid days onsite and days remotely. Coordination with other brand protection associates and Quality with regards to product samples.
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Contributes along with CSL and/or Medical Monitor to development of study design to meet study objectives, development of biomarker/PK strategy in collaboration with Translational Medicine and Clinical Pharmacology (TMCP), providing strategic direction to Biostatistics and Data Operations (BDO) for EDC, edit checks, data quality listings, SAP, Data Mgmt plan, providing strategic direction to Clinical Operations on SDV plan.
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The successful candidate will provide quality expertise to manage and improve processes across Aquestive's development program, ensuring compliance with Good Clinical Practices (GCP), Good Laboratory Practice (GLP), Preclinical stage and GMP for clinical manufacturing oversight.
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quality job Title: scientist Company: Spectrum in Bridgewater, NJ
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