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5+ years of progressive Quality Assurance experience in medical device or pharmaceutical manufacturing organizations. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S. Job Summary: The Manager of Quality is responsible for all aspects of the Quality Management System and its adherence to global standards in addition responsible for employee health and safety.
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Company DescriptionSQA Services is a leading Supply Chain and Quality Assurance consulting firm specializing in the management of Supplier Audit, Quality Engineering, Inspection, and Remediation programs in the Aerospace/Defense, Semiconductor, Medical Device, Pharmaceutical, Cosmetic, and Automotive manufacturing industries.
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Troubleshoot and provide resolution to technical issues to support ramp-up and steady-state operations of two automated pharmaceutical manufacturing facilities. Scope of support will include: Plasma Fractionation and Albumin Purification processes; Process equipment (vessels, centrifuges, filter presses, UF/DF, robotics, COP washers, CIP skids); Distributed Control System (DeltaV) and Process Logic Controllers; Manufacturing Execution System (Siemens Simatic IT); Automation hardware; In Process Testing lab (pH, conductivity, titration); Safety and quality investigations.
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Technical competencies/ Certifications/ Licenses:Technical competenciesMinimum 10 years of experience in Quality Assurance/Compliance in the pharmaceutical, biopharma/biologics or related industry performing direct hands-on work in Quality Assurance, Quality Control, laboratories, manufacturing, supply chain, facilities or engineering preferred.
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Industry background and connections in the Energy, Pharmaceutical, R&D / High Tech, Transportation, Communications and Manufacturing is preferred. The individual will be expected to work at a high tempo and have the ability to engage in conversations with various different stakeholders ranging from IT and Security Operations, Threat & Vulnerability Management, Security Engineering as well as C-suite individuals in security and risk management.
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Assist in complying with any other company and /or departmental objectives as directed by the Group LeaderEducation or Equivalent: Bachelor's Degree in Science or related field required (Chemistry, Microbiology or Biology); A minimum of 3 years related experience in the pharmaceutical manufacturing industry.
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Cutting-Edge Technology: Work with state-of-the-art facilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing. The role is responsible for performing quality activities and maintaining a quality laboratory environment in a sterile pharmaceutical manufacturing facility.
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A minimum of 2 years relevant technical experience in quality oversight of a biotech or pharmaceutical manufacturing operation. Job DescriptionJob DescriptionJob DescriptionSwing Shift - Parenteral Facility (PF)Please note that this will be a typical Manufacturing Swing Shift position.
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Communicate process issues to Manufacturing Manager, Production Shift Foreman and Quality Systems Manager. Gerresheimer is the global partner for pharma, biotech, healthcare and cosmetics with a very broad product range for pharmaceutical and cosmetic packaging and drug delivery devices.
Starting at $20.6 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical prouct development and manufacturing. Perform assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per as per USP monograph / In-house / any other Compendial monographs.
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12+ years of experience in HR, 5+ years in a leadership role, with a strong background in the HR business partner function, learning and development, and manufacturing operations, preferably within the pharmaceutical industry.
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SEGULA TECHNOLOGIES is an Engineering and Design Services company with a proven ability to boost innovation and competitiveness within the major industrial sectors, including Automotive, Aerospace & Defense, Energy, Rail, Naval, Pharmaceutical, and Oil and Gas.
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Job DescriptionJob DescriptionOverviewAs a Procurement Specialist, you will be responsible for managing the sourcing, procurement, and supply of raw materials, packaging materials, and other goods essential for manufacturing high-quality dietary supplement products.
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The QA Manager will delegate responsibilities to direct reports (QA Associate I, II, and III) to achieve the requisite business needs, while providing ongoing support to Manufacturing processes.
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Requirements:Required Qualifications:Manufacturing: 2 years (Preferred)Document management: 2 years (Preferred)Quality assurance: 2 years (Preferred)Knowledge & SkillscGMP compliance within the pharmaceutical manufacturing industry.
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