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Reporting directly to the Senior Manager of Quality, this position collaborates closely with External Manufacturing Organizations (EMO), spanning pharmaceuticals, medical devices/combination products, consumer products/OTC, and biologics sectors, ensuring adherence to cGMP regulations and Bausch Health requirements.
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Minimum of 5+ years of experience working with Pharmaceutical Manufacturing systems (e.g. Data solutions, MES technologies such as Rockwell Automation Pharma Suite, Emerson Syncade, Siemens Camstar, or Werum PAS-X.
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Specifically at the Branchburg site, this position would aid the site adoption and continued enhancement of new and existing systems including Manufacturing Execution Systems (MES), progressing the site's paperless manufacturing objective and Digital Plant Strategy.
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The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing, and metrology, to a broad range of scientific R&D and QC measurements.
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The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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A trusted partner of world leaders in the retail, manufacturing, distribution, travel, services and software industries, Sonata’s software portfolio includes the Brick & Click Retail Platform©, Modern Distribution Platform©, Rezopia Digital Travel Platform©, Kartopia E-commerce Platform©, Halosys enterprise development automation Platform©, CTRM Commodity Trading and Risk Management Platform© and KODO - AI Powered Customer Experience (CX) Platform.
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A minimum of five (5) years experience within a cGMP environment in the biotech/biopharma industry and Cell/Gene Therapy cGMP manufacturing experience preferred. Provide technical expertise in the Technical Operations group, own the process knowledge of the cell and gene therapy manufacturing process technology to support technical activities for transfers into and out of the Raritan facility.
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The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century.
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Handle logistics and coordination of electrical construction activities as per engineering standards, vendor development, with the various departments like manufacturing, QA, QC, R&D for the engineering and Validation Aspects; maintain VMP and other GMP documents, Support Process Validation and Development Studies.
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Comprehensive direct experience in bioprocess development and biological manufacturing. Proven experience in leading teams and collaborating with stakeholders and suppliers to improve biological manufacturing processes and technology transfer.
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Chanel is a world leader in creating, manufacturing and distributing luxury products, including Ready-to-Wear, Accessories, Fragrances, Makeup, Skincare, Jewellery and Watches. US support currently includes Annual sponsorship of the MoMA film program, Tribeca Film Festival programs and Through Her Lens, Support of the Academy Gold Fellowship for Women and Sponsorship of the BAAND Together Dance Festival at Lincoln Center.
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The Injection Molding Process Engineer is a "hands-on" position that plans, directs, and coordinates manufacturing equipment and processes to produce high-quality injection molded products. Strong and diverse technical background in injection molding processing, tooling, equipment, materials, manufacturing, and quality.
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At least 5 years of experience in a manufacturing environment, with a proven track record in digital innovation. JOB CATEGORY: Engineering - Industrial / Manufacturing. Strong technological proficiency, including familiarity with programming (e.g., Google Appscript, Python), data analytics (e.g., DOMO, Tableau, Looker Studio), and IoT architecture solutions like MQTT communication protocol.
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Associates or no degree required with 4 or more years of experience working in the pharmaceutical industry in Quality Control/Assurance or Manufacturing, and 2 or more years in a leadership role.
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manufacturing job Title: manufacturing assistant Company: Ashley Furniture Industries Inc in Bridgewater, NJ
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