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Your technical expertise as a QA Specialist I in the area of cGMP, clinical setting will contribute to our client's innovative therapies which will impact the quality and duration of life. 0-3 years' work experience in a cGMP related industry or in a clinical setting is preferred.
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The primary responsibility of the Data Verification Specialist is to ensure the Chemical Quality (CQ) laboratory is in compliance with cGMP technical requirements, training, data review, pre and post sterile product testing, investigational testing and investigations, and completion of area related projects.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Work with Quality management to ensure quality systems support cGMP manufacturing of pre-clinical to commercial products. Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe.
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Adhere to cGMP guidelines, SOP's and plant policies/rules. Responsible for accurate and timely documentation of work in batch records, log books and other official documents. Adhere to cGMP guidelines, SOP's and plant policies/rules.
$19 an hourExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The Material handler is responsible for the distribution of materials during production activities that are conducted in accordance with cGMP standards of operations. Complete cGMP Paperwork thoroughly and promptly.
Full-timeRemoteExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Utilizes manufacturing equipment and in-process instrumentation to manufacture medical devices in accordance to current Good Manufacturing Practices (cGMP), company policy and safety requirements.
Full-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Ensure compliance, as set forth in internal quality protocols and SOPs including cGMP and FDA regulatory guidelines, within the areas of responsibility, and document out of specification conditions with deviations, CAPAs and Change Controls as appropriate.
Full-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Ensures that the quality management system demonstrates regulatory compliance per GLP/GCP/cGMP/GXP, ISO, and other applicable regulations for the Luminex sites in Chicago, Madison and Toronto. 10+ Years of Experience in Quality Assurance or Regulatory Affairs activities in a cGMP Medical Device or Pharmaceutical environment.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Draft and revise manufacturing SOPs/work instructions to support process improvements and maintain cGMP compliance. Knowledge of cGMP regulations and SOP adherence. Production Manager or Manufacturing Manager experience in the medical device industry, with likely cleanroom experience.
$200,000 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Draft new and revise existing manufacturing SOPs/work instructions to support process improvements and maintain cGMP compliance. Rigorous adherence to SOPs and cGMP regulations with the ability to accurately complete documentation associated with the manufacturing process in a timely fashion is required.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Responsible for reviewing Medical complaints that involve a non-medical quality related problem. Product complaint documentation, investigation, and review of all non-medical complaint content. Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GCP. This requires good analytical skills, technical writing and good documentation.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines.
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Familiarity with relevant regulations and standards (e.g., ISO, FDA, cGMP). Proficiency in using QA software tools and electronic Quality Management Systems (eQMS) is a plus. Knowledge of Quality Management Systems (QMS), CAPA processes, and audit procedures.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Preferred degree in technology or scientific background (MLT, LPN, RN)." Interface with internal the client's customers such as physicians, nurses, pharmacists, hospital personnel, risk managers, purchasing agents, sales representatives, general public, manufacturing sites, technical support, commercial organization and PV regarding the client product complaints.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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You will follow company standard operating procedures and policies and other cGMP related procedures. The company's disruptive and innovative products compete in the Functional Beverage and Active Nutrition segments, under three consumer-loved brands: C4® (one of the fastest-growing energy drink brands in the United States and the #1 selling global pre-workout brand), XTEND® (the #1 post-workout recovery brand in the United States), and Cellucor® (an award-winning sports nutrition brand created in 2002.
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cgmp job in Austin, TX
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