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The Material Handler Floater is responsible for handling raw materials and finished goods as well as loading and unloading trucks. Responsible for safe truck loading and unloading, staging materials in the warehouses, getting raw materials and/or finished products ready for shipping to customers, internal warehouse transfers and/or production.
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Perform assigned sampling, physical, chemical tests and assay on packaging materials, raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per as per USP monograph / In-house / any other Compendial monographs.
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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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Transport finished goods and or raw materials over land to and from manufacturing plants or retail and distribution centers. Advancement Potential, and an Excellent Quality of Life. Our company is growing rapidly, and we are seeking an experienced Local Delivery Non-CDL Driver in our Branchburg, NJ location.
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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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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.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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Manufacturing quality technician. Employee is responsible to follow and uphold all Food Safety, Food Quality, Occupational Safety, Health and Environment policies and procedures as pertains to role.
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The primary objective of the QC Packaging Technician is to identify and rectify defects or deviations from established quality criteria to maintain high product quality. The Quality Control Packaging Technician will play a critical role in ensuring products are packaged correctly and meet quality standards before they are shipped to customers.
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The primary purpose of the job is to perform testing and make calculated decisions on the acceptability of process validation samples, raw materials, finished products, stability samples, and developmental samples in a regulated laboratory environment in support of timely disposition of manufactured products.
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Performs routine analytical tests of pharmaceutical raw materials, in-process samples, blends, finished products, and stability samples using instrumentation such as HPLC, UPLC, GC, UV/VIS, FTIR, dissolution apparatus, particle size analyze, etc.
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Job Description: Assistant QC ScientistOnsite role, Warren NJWork Schedule: Mon - Fri, AM - :PM EST Purpose:The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products.
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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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raw job Title: quality in Somerset, NJ
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