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Job Title: QA/QC Analyst Company : AstraZeneca Overview : The QA/QC Analyst at AstraZeneca is likely responsible for ensuring the quality and compliance of products and processes within the company's pharmaceutical manufacturing or research facilities.
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Responsibilities include but are not restricted to the following: collaborate with R & D for new product transfer and consult to resolve issues with QC test strategies; collaborate with manufacturing, process engineering and QA for non-conforming product troubleshooting and resolution; develop strategy, organization, including process improvement to ensure the Quality Control meets business expectations.
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Our client, an industry-leading CPG company, is seeking a QA/QC Manager for their state-of-the-art manufacturing plant with top-of-the-line technology. Our client, a start-up CPG company, is seeking an EHS Manager for their state-of-the-art greenfield manufacturing plant with top-of-the-line technology.
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As a Quality Control Professional , you will be working in one of these market sectors: Commercial Buildings (healthcare, higher education, mission critical, and retail), Advanced Technology (semiconductor manufacturing, renewable energy), or Industrial (pulp and paper manufacturing.
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Collaborates with and provides open, honest, technically accurate information to support teams (Eng, Fac, PS, QA, QC, SC) during scheduling meetings, event/deviation investigations and process/ equipment troubleshooting.
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BioPharma, Pharma, Quality, ISO, FDA, QA, QC, CMO, Sterile Aseptic, filling, BFC, remediation. Managers from QA, QC. Six Sigma, Lean Manufacturing , continuous improvement, etc.
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The QA Specialist will interact with manufacturing personnel and Quality Engineers to provide guidance necessary to maintain and improve CGMP compliance at the company. BS or BA degree in Science or Engineering with 0-2 years of GMP experience; QA/QC role preferred.
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Responsible for QA/QC process adherence. The Senior Process Engineer will lead piping design project teams to create world class designs for new projects, alterations and redevelopments on a variety of projects including aerospace, power, process, corporate, healthcare, pipeline, airports, industrial, manufacturing, government and military facilities.
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5) Charter cross-functional tech transfer teams comprising of R&D, QA, QC, Regulatory Affairs, and operations. 7) Be accountable for site process control strategy document, technical transfer change controls and protocols and ensure that the manufacturing batch record meets established conditions as defined in the CMC documentation.
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The QA Documentation Specialist is responsible for developing, implementing, and maintaining end-to-end Quality Assurance document systems at Chemical Guys. We manufacture our auto-detailing chemicals right here in Carson, CA and this is a great opportunity to grow and work alongside our both our quality (QA/QC) and manufacturing teams.
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The qualified candidate will act provide quality assurance support quality systems and compliance activities working cross-functionally with R&D, Product/Process Development, Manufacturing, Supply Chain, QC and QA.
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Lastly, you will issue corrective action notices to employees within the fabrication operation, when necessary, to enforce company and/or project guidelines and policies related to safety, HR, QA/QC, attendance, and production.
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Provide required support to the QA/QC team to resolve internal or external non- conformities. Develop methodologies for transferring procedures or biological processes from laboratories to commercial-scale flavor manufacturing production.
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Inspections and Sign Off: Participate in Design Verification walks that include Initial Inspections, Follow up and Final Inspection in coordination with QA/QC Trade Partners. Minimum of 3-5+ Years' Experience in executing or managing construction in the Semiconductor, Industrial, Chemical, Gas and Oil or other manufacturing markets.
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Responsible for the management of Quality Assurance and Quality Control (QA & QC) staff supporting the manufacturing plant. Ensures the organization attracts, develops and retains the best talent for QA/QC teams.
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