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Follow cGMP/cGLP requirements and execute/document all testing in the laboratory according to these standards. Adhering to cGMP/cGLP documentation practices. Experience working in a cGMP/cGLP environment.
$60,000 - $68,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Quality Operations Specialist in this role is responsible for performing various and complex investigations that ensure compliance with CGMP, implemented standard operating procedures, validated processes and established facility and quality systems.
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Monitor batch processing activities to ensure compliance with established procedures, batch records, and cGMP requirements. Participate in departmental and interdepartmental teamwork as assigned by the QA Supervisor/Manager, which may include writing deviations, performing investigations, writing change controls, executing action items, revising SOPs, and other GMP documents.
TemporaryExpandUpdated 12 days ago - UpvoteDownvoteShare Job
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Expertise in Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and related federal, state and local laws, codes, regulations and regulatory requirements. High school diploma and 5-8 years of maintenance supervisory experience, preferably in a pharmaceutical, food, or cosmetic manufacturing environment.
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Ensure that all maintenance activities comply with relevant regulatory standards, including FDA, cGMP, and other applicable guidelines. Experience with Pharma, & cGMP is preferred. Working knowledge of electrical, mechanical and basic PLC programming/troubleshooting.
$125,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Execute manufacturing processes with strict adherence to cGMP and safety guidelines. Join Our Team as a 2nd Shift Manufacturing Technician! Our renowned biopharmaceutical company, with over 40 years of expertise in plasma-derived products, is seeking dedicated individuals like you to join our team.
$47,000 - $54,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The candidate will also be responsible for ensuring that all suppliers meet the necessary FDA, cGMP and ISO requirements. Ensure suppliers meet the necessary FDA, cGMP and ISO requirements.
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Knowledgeable with the following: ultrafiltration and other filtration systems, cGMP facility design (cleanrooms, ISO classes, HVAC), utility systems common to the biopharmaceutical industry (e.g., WFI, RO water, compressed gases), clean-in-place (CIP) & (COP) equipment and cleaning cycles, clean room design, TCUs and operating principles.
ExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Clearing and disposing of waste from diverse company locations, including those adhering to current Good Manufacturing Practices (cGMP) Dispose of waste in various manufacturing locations, including cGMP areas.
Full-timeExpandUpdated 19 days ago - UpvoteDownvoteShare Job
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Transport full pallets of finished goods to storage and staging areas with power and pallet jacks in a timely manner, observing all safety regulations and ensuring all cGMP and quality standards are met.
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In addition, you will ensure quality of product in accordance with all NYBC's Standard Operating Procedures, work instructions and regulatory standards, as well as following and practicing cGMP in all work.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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OQuality targets; Manage Quality Systems to meet FDA / OTC, China NMPA, and Health Canada cGMP compliance. Performs as overall Operations leader for Melville 350 Manufacturing Plant and manages flagship complex operations in alignment with the Global and North American Supply Chain strategies and operating plans to deliver key factor results in Safety, Quality (cGMP requirements), Customer Service and all aspects of Plant Operating Costs across a $70MM + Operating budget and 700+ employees.
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Perform laboratory work in a cGMP setting, primarily working with adult cell culture (MSCs) and differentiation, following bio- manufacturing procedures and manufacturing schedules to facilitate on-time delivery of high-quality finished products for clinical use.
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That have received the above mentioned training upon hire will receive annual refresher training that covers the OSHA HAZWOPER standard and the requirements of RCRA. Hours per Day 8 Hours per Week 40 Total Hours 2,096.00.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Plan and schedule maintenance work and mechanic and custodial resources to meet maintenance department goals. Incumbents may be exposed to toxic materials, toxic gases, electrical hazards, and dangerous tools and equipment.
$80,000 - $95,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago
cgmp job in Melville, NY
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