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The Quality Assurance Specialist works closely with all facility personnel to ensure excellent quality performance and full compliance with cGMP and Food Safety requirements.
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Five (5) to seven (7) years of quality assurance experience in the Pharmaceutical industry providing oversight to Manufacturing Operations, QC, and other cGMP areas. Performs independent technical review of documentation including Batch Production Records during and post-execution of cGMP activities.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Perform start up and commissioning activities, as required and work in a collaborative team environment and interact with other support groups such as Engineering, Validation, Quality Assurance and Metrology.
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The Sr. Associate Compliance provides scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product quality complaints; ensures compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP) and Quality Management System standards, compiles monthly Quality metrics for internal and corporate review, and analyzes trends to implement corrective and preventive actions to mitigate adverse trends.
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We have an urgent requirement for Quality Assurance Associate for one of our medical device client. Job Title: Quality Assurance Associate. Manage quality status of WIP and finished good materials on physical inventory and in inventory system (JD Edwards.
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The Quality Assurance Manager is an exempt position that is paid semimonthly. Leads quality assurance activities for medical device, over-the-counter, and prescription drug products.
Full-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Tofurky is looking for a Quality Assurance (QA) Manager to join our QA Team. The QA Manager will be responsible for overseeing the food safety and quality systems within Tofurky’s plant operations located in Hood River, OR. As an integral member of the QA Team, you’ll work with a core quality assurance team, as well as working cross-functionally to maintain, develop and enhance our food safety programs.
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Provide proactive quality assurance and risk assessment using FMEA, HCCAP, and Quality by Design in compliance with client and cGMP policies, procedures, rules, and regulations.
$75,000 - $85,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Quality Specialist II will assist the Quality Assurance team with special projects as required. Quality Assurance Specialist II. Responsible for ensuring compliance to FDA and cGMP standards for Quality Control, including continuous training.
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Act as technical liaison for Quality Assurance department in the absence of the Quality Assurance Manager: externally with customers and vendors; internally with production, R&D, marketing, and procurement for all quality processes.
$68,000ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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High level job accountabilities included activities related to sterility assurance, manufacturing oversight, quality system and release of raw materials. Interact with manufacturing management to provide quality perspective on routine operations and support systems.
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Report any errors or discrepancies to the line leader, Supervisor, Director of Quality and/or General Manager. Basic knowledge and understanding of cGMP. Inspection of initial product produced as it is bottled and released off the production line, checking for correct content, volume fill level, bottle size, verification of label, correct batch number, expiration date, verification packaging conforms to customer purchase order specs.
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Strong knowledge of chemical process safety, validation, and quality assurance. Experience in a Pharmaceutical cGMP or other regulated environment. Write, review, and revise SOPs (Standard Operating Procedures) and/or work instructions for cGMP (Good Manufacturing Practices) manufacturing of commercial product.
$91,000 - $115,750 a yearExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Must have a minimum of one (1) year work experience in the biologics industry, preferably in a donor center, and a minimum of one (1) year quality assurance-related work experience. Provides advice and consultation to other management team members regarding daily quality assurance issues including donor suitability and/or product quality.
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A minimum of 3 years’ experience in a GMP manufacturing environment with a bachelor’s degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical engineering, Biochemistry or related field or seven years of experience in a clinical quality assurance environment.
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