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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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The successful candidate will oversee technical installation of Manufacturing Operational Technology (OT) hardware and software solutions that support Pharma Services Group (PSG) GxP compliant systems, including the following examples of OT devices Manufacturing Execution Systems, Computerized Maintenance Monitoring Systems, Advanced Analytic Systems, Serialization Systems, etc.
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The Sr. Manager will be responsible for all processes associated with delivery, receipt, and storage of patient apheresis and distribution of clinical and commercial cell therapy drug products that will be manufactured within a state-of-the-art multi-product cell therapy manufacturing facility.
$90,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Continuous innovation in passive component function integration, miniaturization, and manufacturing automation, cutting edge WSS and amplifier technology and comprehensive optical, mechanical, electrical and software integration capabilities enable us to serve the needs of high-density, high-bandwidth, and flexible optical networks.
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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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This exciting new role sits on our E2E Advanced Therapies Cell Therapy MAKE Manufacturing Team and works with the Site Lead of Supply Chain Systems. Minimum 4 years of relevant work experience in Pharmaceutical Manufacturing System Processes (GxP) Systems environment and related Master Data Management.
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Responsible for revenue and contribution margin generation at assigned accounts and newly discovered customers for contract drug delivery service businesses such as Vancouver Labs™, Birmingham Labs™, oral development services, and custom polymer development and manufacturing services.
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Act as an Optical Engineer for complex photonics programs in areas that can include free-space optical communications, laser transmitters for remote sensing, and RF photonics. The Optical Scientist position is intended for an individual who is interested in supporting and leading programs devoted to the design, development, and use of free-space photonics.
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Leads the Cell Therapy manufacturing sites ecosystem as an IT manager with ownership of local products and works toward re-defining to a platform or standard product according to JJT strategy. Johnson & Johnson Innovative Medicine is recruiting a Technical Product Senior Manager - CAR-T Manufacturing Systems to support the North America (NA) region for our Advanced and Cell Therapy Manufacturing business in Raritan, NJ.
$118,000 - $203,550 a yearExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy.
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Partner with Manufacturing, Product Support, Microbiology, Regulatory Affairs, Quality Control Labs, Engineering and Compliance. Utilize multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), and international organization for standardization (ISO.
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Apply Job Type Full-time Description Position SummaryThe Upstream Manufacturing Scientist is responsible for executing mammalian cell culture processes and producing recombinant proteins for a wide range of mammalian based biosimilars.
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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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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. Works closely with quality, manufacturing, Global Regulatory Affairs (GRA), and technical staff from global locations within industrial network, contract manufacturing organizations (CMOs), and alliance partners to author high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers.
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A cornerstone of this roadmap is the acceleration of its data organization and adoption of artificial intelligence (AI) and machine learning (ML) solutions, to accelerate R&D, manufacturing and commercial performance and bring better drugs and vaccines to patients faster, to improve health and save lives.
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pfizer manufacturing jobs in Raritan, NJ
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