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The North Creek Manufacturing Facility at Pfizer is seeking a highly motivated Manufacturing Associate that desires the opportunity to significantly contribute to the development and commercialization of transformative cancer therapies.
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Ginkgo has built a platform for "cell engineering" to use AI/ML tools for DNA design, long DNA synthesis and assembly, next-gen sequencing, automated culturing, assay development, high-throughput high-content screening to advance pre-clinical research and development as well as manufacturing process optimization across therapeutic modalities.
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The newly created Manufacturing Intelligence organization within Pfizer’s Global Technology & Engineering will help to drive Pfizer Global Supply toward ‘Industry 4.0’ capability through Big Data, Process Analytical Technology, Advanced Process Control, Artificial Intelligence and Robotics.
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Building Repairs, Building Repairs, Business Overheads, Cabinetry, Color Schemes, Color Selections, Communication, Computerized Maintenance Management Systems (CMMS), Customer Satisfaction, Deadline Management, Detail-Oriented, Dexterity, Environmental Conditions, Exterior Design, Exterior Painting, Finishing Materials, Furniture Building, HVAC Systems, Ladders, Life Sciences Industry, Manufacturing, Manufacturing Environments, MAXIMO CMMS, Organizing, Painting Process + 9 more.
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Good knowledge of pharmaceutical manufacturing and related unit operations is also a plus. This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The successful candidate will be a member of the SMO team and will have the responsibility to develop and implement Process Analytical Technologies, and support robotics, cobotics and lab automation initiatives for SMO manufacturing and quality operations.
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Define and drive the analytical development strategy in full alignment with the other CMC and associated functions (Drug Product Design, Clinical and Commercial Supply Chains, Nonclinical and Clinical Development, Quality Assurance, Regulatory Affairs, Pfizer Global Supply for Commercial Manufacturing.
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Youre considered fully vaccinated two weeks after you receive the second dose of a two-dose vaccine series (e.g., Pfizer or Moderna) or two weeks after a single-dose vaccine (e.g., Johnson & Johnson/Janssen.
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As a member of the Pfizer Drug Substance and Active Biological Ingredients (ABI) team, you will be accountable for activities involved in the production of many of Pfizer's products, specifically with regard to technology transfer.
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Ensure data quality, integrity and security best practices conform to data governance best practices Establish and maintain references, ontologies, data types, dimensional models, and lineage relevant to Pfizer Commercial Analytics Data products.
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The scope of responsibility spans drug discovery and development, medical affairs, marketing and brand management, sales, managed markets, manufacturing operations, trade and distribution, and finance.
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Founded in 2016, our customers include industry leaders such as Atlas Copco, Pfizer, and Toyota, to name a few. To help our clients transition seamlessly, the Solutions Engineer’s role is instrumental in understanding, translating, and tailoring our B2B SaaS product to manufacturing companies’ individual needs and contexts.
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Make product Quality decisions leveraging comprehensive knowledge of Quality/Manufacturing principles, prior work experience and concepts in other technical areas while ensuring compliance to global regulatory and Pfizer requirements.
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Setup and operate a CNC lathe (Mazak), and manual machines such as lathes, mills, and potentially a cylindrical grinder in the manufacturing of light industrial parts. Drawing on nearly four centuries of collective experience across Wabtec, GE Transportation and Faiveley Transport, the company has unmatched digital expertise, technological innovation, and world-class manufacturing and services, enabling the digital-rail-and-transit ecosystems.
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Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring.
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Maintain written records of all experimental work in accordance with Good Lab Practices/ (Current) Good Manufacturing Practices (GLP/GMP) and departmental Standard Operating Procedures. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure.
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