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PSEG offers a unique experience to our more than 12,000 employees - we provide the resources and opportunities for career development that come with being a Fortune 500 company, as well as the attention, camaraderie and care for one another you might typically associate with a small business.
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QA Scientist I: A Bachelor's degree in Medical Technology/Medical Laboratory Scientist, Biology, Chemistry or related field and a minimum of 1-3 years' experience with QC, GMP, GDP, and medical device company is required.
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The QA Lab Oversight Specialist role is an exempt level position with responsibilities for providing quality oversight over the site Quality Control laboratories responsible for testing of pre-clinical, clinical, and commercial stage CAR-T cellular therapy products.
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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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RCM is seeking a highly motivated and detail-oriented Technical Support Specialist to join our client's growing team in Branchburg, NJ. This full-time contract position offers a competitive salary of up to $45 per hour and the opportunity to play a vital role in a GMP-regulated pharmaceutical (API) manufacturing environment.
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The Radiologic Technologist & Medical Support Specialist performs routine will perform routine x-ray examinations in accordance with Concentra policies, practices, and procedures and applicable regulations under direct supervision of the treating clinician, as well as supports in other needed areas of the facility.
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Trains, supervises and evaluates the performance of QA inspectors, QA Specialist and QA Auditors to assure compliance with Standard Operating Procedures (SOPs)/cGMP. + Initiates, investigates and completes CAPA for all QA unplanned deviations under the guidance of QA Manager.
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Relevant experience includes Business Analyst/Manager, Management Analyst, Financial Analyst, QA Analyst, Accountant, and IT Project Manager/Lead, Project Control Specialist or related occupations.
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Specialist, QA Operations, is responsible for quality oversight of Cell Therapy Development Operations (CTDO) activities in accordance with BMS policies, standards, procedures, and Global cGMP requirements.
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Specialist, QA Operations, is responsible for quality oversight of Cell Therapy Development Operations (CTDO) activities in accordance with Client policies, standards, procedures, and Global cGMP requirements.
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This is NOT a QA/Testing role. Web Accessibility Specialist (WAS) Certification. Senior Accessibility Specialist (Onsite) Prior experience with project management platforms (such as Asana and Basecamp), collaboration platforms (Slack) and bug-tracking systems (Jira.
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Minimum of 7 years relevant working experience in a pharmaceutical or biotechnology company of which preferably 3 years in validation or QC, and in QA/CSV. minimum of 7 years relevant working experience in a pharmaceutical or biotechnology company of which preferably 3 years in validation or QC, and in QA/CSV.
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Manage the QA review and approval of incoming material, labeling, line opening/closing, in-process and finished device history records, including BASIS release and ERP transactions. Support the QA review and approval of product, process, facility and equipment validation protocols and reports following current quality management system requirements.
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The QA Microbiology Specialist is an exempt level position with responsibilities for providing microbiological oversight and contamination control of the production of autologous CAR-T products for clinical trials and commercial operations in a controlled cGMP cleanroom environment.
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RoleThis is an extraordinary career opportunity for a Senior Quality Assurance (QA) Specialist who will be responsible for supervising and leading business activities to ensure a state of continuous compliance.
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qa specialist jobs in Warren, NJ
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