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Operates general analytical instruments during raw material, IP and FP testing such as High Pressure Liquid Chromatography (HPLC), Ultra Performance Liquid Chromatography (UPLC), Gas Chromatography (GC), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra-Red Spectroscopy (IR), Malvern Mastersizer, Thin Layer Chromatography (TLC) and dissolution apparatus (Distek); Creates and uses custom fields in Empower software while operating HPLC/UPLC and GC instruments.
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Performs testing for raw materials, packaging components, IP, FP and/or ST samples including dissolution, assay, Related Compounds analysis, content/blend uniformity, particle size distribution by Malvern/Sieve, bulk and tap density, cleaning validation and other tests according to the analytical methods, United States Pharmacopeia (USP) procedures in a regulated laboratory environment.
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Hands on experience to Perform/develop assigned physical and chemical tests on raw materials and active pharmaceutical ingredients using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine instruments.
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The QC Chemist II performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. Performs assigned sampling, physical, chemical tests and assay on raw materials, active dietary ingredients, in-process, finished, and stability products in an FDA GMP regulated lab environment.
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Supports department and Company initiatives to ensure quality assurance oversight and adherence to cGMP for various departments and functions such as warehouse, manufacturing processes, inspection, labeling and packaging, batch record review, batch disposition and product distribution as applicable.
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Perform assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques.
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The qualified candidate will also work closely with the Personal Care product development team to evaluate new raw materials and establish a mechanistic understanding of these ingredients in skin care applications.
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Conduct various scientific analyses to assess the quality of raw materials, in-process materials, and finished products. Maintain organized raw data records for review purposes. Promptly escalate quality or compliance concerns to Line Manager and Senior Management.
$40 - $44 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Inspector performs calibrations & measurements on raw materials, bulk products, finished products and packaging components as required in batch records and SOP’s. Performs calibrations & measurements on raw materials, bulk products, finished products, and packaging components as required in batch records and SOP’s.
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Under the supervision of the Quality Manager / Quality Supervisor the QC Inspector ensures compliance with cGMP and company policies, procedures, and specifications. Minimum 1 - 3 years’ experience in Quality Control environment preferably in cosmetics, personal care, pharma, or food packaging industry with exposure to FDA and cGMP regulations.
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Actalent Quality Assurance Specialist Plainsboro , New Jersey Apply Now Actalent is hiring a Compliance Specialist for one of NJ's largest fragrance companies! Previous experience within a quality assurance team.
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Senior Consultant | Payments | ACI MTS payment product tester/ Quality Engineer (QE) Support requirement workshops, help define the problem statement, provide solution alternatives, create detailed design documentation, implement deployment plan, and support knowledge transfer with the objective of providing high-quality and value-adding consulting solutions to customers within the guidelines, policies and norms of Infosys.
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Optimize raw material quality and service: Work with technical teams to accelerate adoption of alternate products and suppliers. Related supply chain experience in the space operating around raw materials, suppliers, supplier relationship management and supply chain best practices (> 10 years.
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Include raw materials and Finished Products. Our global team of over 2,500 employees drive our capabilities in product development, product formulation, strategic sourcing, manufacturing, packaging design, brand marketing, project management, quality assurance, compliance, distribution, and logistics.
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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. Position Summary 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.
$22 - $24 an hourExpandApply NowActive JobUpdated Today
raw job Title: quality in Monroe, NJ
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