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B.A./B.S degree in Chemical Engineering, Biology, or similar relevant field with at least 6 years of direct GMP manufacturing experience in a biotechnology manufacturing facility or Pilot Plant OR a High School Diploma with 10 years of experience in protein purification in Biotech/Pharmaceutical industry.
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2-4 years’ experience in Formulation work in Pharmaceutical Industry, Dietary Supplement Industry, Food Industry or a related fieldHands-on experience with beverage, gummy, stick packs, tableting and capsules preferredWorking knowledge of regulations pertaining to dietary supplements manufacturingKnowledge of good manufacturing practices (GMP.
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ZS is looking for a Decision Analytics Consultant in the ZS Supply Chain and Manufacturing practice with an experience in pharmaceutical drug development and tech transfer. The primary responsibility of this role is to deliver projects in pharmaceutical CMC development area for ZS Supply Chain and Manufacturing clients.
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8+ years of experience in Facility/Maintenance/Engineering, preferrable pharmaceutical manufacturing. Eugia is US-based independent specialty pharmaceutical company focused on generic sterile injectables, oncology, hormones, and ophthalmic medicines.
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Minimum 1 year pharmaceutical manufacturing experience- preferably in compression/encapsulation/coating. Supports and assists in the manufacture of pharmaceutical products according to Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs) and batch record specifications.
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Support start-up of biotechnology, cell & gene therapy, and pharmaceutical manufacturing facilities. 7-15 years of experience in the biotech/biologics, cell/gene therapy, and/or pharmaceutical/drug sectors.
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Bachelor's degree in Engineering (Mechanical Engineering, Pharmaceutical Engineering, Chemical Engineering, Biomedical Engineering). On-site work in Plainsboro, NJ M-F normal business hours For the visual inspection related positions (Manufacturing Engineer II), the top skills are.
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10+ years of experience, preferrable pharmaceutical manufacturing. Perform manufacturing and facility equipment maintenance, installations and repairs as needed by customers or determined through routine audits including but not limited to carpentry, electrical, plumbing (boilers, chillers, dust collector, air handling unit, fire alarm system etc) and light construction.
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These range from incubator companies focused on technology and cutting-edge diagnostics, to Fortune 500 entertainment, pharmaceutical, consumer products, publishing, consulting, manufacturing, and financial services firms.
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0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Responsible for accurately maintaining legible and accurate records, required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and Health and Safety requirements.
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Complete projects aimed to evaluate, analyze, and improve existing processes, support the development of new manufacturing processes, and manufacturing process troubleshooting. Statistical process control: analyze and trend existing process parameters, process inputs and outputs to improve manufacturing yields, reduce manufacturing scrap, and error proof manufacturing processes.
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We have partnered with a large Pharmaceutical Manufacturing company in the Monroe, NJ area to provide them with a Senior Financial Analyst. The Senior Financial Analyst in the Financial Planning & Analysis group plays in integral role in preparing, validating and analyzing local and corporate management reporting and supporting various annual and quarterly financial planning activities (e.g., budgeting, and forecasting.
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Leveraging and developing relationships to build long-term business partnerships in key industry sectors including energy, waste, cement/lime, oil/gas, chemical manufacturing, and pharmaceutical.
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Support projects to implement statistical process control (as necessary), analyze and trend existing process parameters, process inputs and outputs, improve manufacturing yields, reduce manufacturing scrap, and error proof manufacturing processes.
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Strong technical background in assay development, pharmaceutical analysis, bioassay, impurity testing, microbiology support, quality control, and stability management. Work closely with Manufacturing, Tech Transfer, QA, and Regulatory departments to ensure appropriate testing information is effectively communicated and documented.
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pharmaceutical manufacturing jobs in Cranbury, NJ
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