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Must possess certification as required by state law which may include building inspector, building plans examiner, residential electrical inspector, plumbing inspector, mechanical inspector, mechanical plans examiner, plumbing plans examiner, electrical plans examiner, chief electrical code analyst, chief building code analyst, chief plumbing code analyst, chief mechanical code analyst, code enforcement and administration professional.
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Minimum Requirements: The QA Supervisor must have at least 5-7 years of experience in an FDA regulated manufacturing environment, with 5 years specifically in Quality Assurance or Quality Control.
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Working with Production, Regulatory Affairs, Marketing, New Product Development and other necessary departments to maintain awareness of Quality Systems activities. Conducting investigations, assessing and closing deviations, determining impact of the issues that could affect product quality, safety and purity.
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Minimum Requirements: The QA Supervisor should have a minimum of 5-7 years of experience in a FDA regulated manufacturing environment, with at least 5 years in Quality Assurance or Quality Control.
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Developing and deploying the Quality systems to ensure products conform to defined requirements. Product quality and conformance to government regulations, industry standards, and Company policies.
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Minimum Requirements: The QA Supervisor must have at least 3-5 years of experience in an FDA regulated manufacturing environment, with 3 years specifically in Quality Assurance or Quality Control.
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Today, our 82,000 associates serve more than 10 million customers a week across 10 Southeastern and Mid-Atlantic states.
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An Associate degree with 10 plus years in pharmaceutical manufacturing experience will be considered. Education and Experience: BS Degree or BA Degree with a Science major or concentration and continuing education credits in the pharmaceutical industry through a reputable professional society.
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Manages brand portfolios to maximize long-term sales and profit; develop and execute portfolio strategy to build long-term brand health.
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Manages brand portfolios to maximize long-term sales and profit; develop and execute portfolio strategy to build long-term brand health.
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The QA Supervisor supports all of the day to day operations, techniques, and activities associated with those departments that are used to fulfill the Quality Assurance requirements of the product and/or service.
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Must have at least 3-5 years of experience in an FDA regulated manufacturing environment, with 3 years specifically in Quality Assurance or Quality Control. Ensure cross training is performed and documented for individuals within the QA Document Specialist group.
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Job Title Quality Assurance Document Supervisor. Primary Skills Quality Assurance Professionals. Industry(ies) Biotechnology/ Life Sciences,Pharmaceutical. Track individual reviewer metrics to determine if additional training or guidance is needed.
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Reviewing of PMs, Pest Control, Calibration records, etc. Must periodically work second and third shift hours in support of personnel on those shifts. Prior FDA or equivalent inspection experience is highly recommended.
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Manages brand portfolios to maximize long-term sales and profit; develop and execute portfolio strategy to build long-term brand health.
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Title: quality inspector Company: Consolidated Aerospace Manufacturing in Lancaster, SC
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