Position OverviewThe Technician 3 Maintenance is responsible for the installation maintenance and repair of process related systems/equipment. Ensure these systems meet the stringent requirements of pharmaceutical manufacturing. Also responsible for conducting regular inspections and
Position OverviewThe Technician 3 Maintenance is responsible for the installation maintenance and repair of process related systems/equipment. Ensure these systems meet the stringent requirements of pharmaceutical manufacturing. Also responsible for conducting regular inspections and
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Position OverviewThe Quality Control group at FDBU group is seeking a Lead QC Associate II Raw Materials at our Bioprocess Innovation Center in Morrisville NC. The QC Lead Associate II is responsible for sampling testing and releasing incoming raw materials in compliance with GMP reg
Position OverviewThe Quality Control group at FDBU group is seeking a Lead QC Associate II Raw Materials at our Bioprocess Innovation Center in Morrisville NC. The QC Lead Associate II is responsible for sampling testing and releasing incoming raw materials in compliance with GMP reg
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Position OverviewThe Quality Control group at FUJIFILM Biotechnologies in Research Triangle Park NC is seeking a Lead QC Associate II Raw Materials at our Bioprocess Innovation Center in Morrisville NC. The QC Lead Associate II is responsible for sampling testing and releasing incomi
Position OverviewThe Quality Control group at FUJIFILM Biotechnologies in Research Triangle Park NC is seeking a Lead QC Associate II Raw Materials at our Bioprocess Innovation Center in Morrisville NC. The QC Lead Associate II is responsible for sampling testing and releasing incomi
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Position OverviewThe Quality Control group at FUJIFILM Biotechnologies in Research Triangle Park NC is seeking a Lead QC Associate II Raw Materials at our Bioprocess Innovation Center in Morrisville NC. The QC Lead Associate II is responsible for sampling testing and releasing incomi
Position OverviewThe Quality Control group at FUJIFILM Biotechnologies in Research Triangle Park NC is seeking a Lead QC Associate II Raw Materials at our Bioprocess Innovation Center in Morrisville NC. The QC Lead Associate II is responsible for sampling testing and releasing incomi
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Position OverviewThe Scientist II conducts research and development activities focusing on new product development technical product support and process improvements. Tasks include experimental design data analysis cell culture experiments and maintaining good laboratory practices. Th
Position OverviewThe Scientist II conducts research and development activities focusing on new product development technical product support and process improvements. Tasks include experimental design data analysis cell culture experiments and maintaining good laboratory practices. Th
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Position OverviewThe Scientist II conducts research and development activities focusing on new product development technical product support and process improvements. Tasks include experimental design data analysis cell culture experiments and maintaining good laboratory practices. Th
Position OverviewThe Scientist II conducts research and development activities focusing on new product development technical product support and process improvements. Tasks include experimental design data analysis cell culture experiments and maintaining good laboratory practices. Th
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Position OverviewThe Lead Associate 3 Quality Control (QC) Microbiology oversees and guides the critical operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting microbiological assays as well as effectively trains junior analysts
Position OverviewThe Lead Associate 3 Quality Control (QC) Microbiology oversees and guides the critical operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting microbiological assays as well as effectively trains junior analysts
Position OverviewThe Supervisor QC Microbiology leads a team of microbiology analysts to execute GMP testing environmental monitoring and microbiological control programs supporting clinical and/or commercial manufacturing. This role ensures cGMP compliance data integrity safety and r
Position OverviewThe Supervisor QC Microbiology leads a team of microbiology analysts to execute GMP testing environmental monitoring and microbiological control programs supporting clinical and/or commercial manufacturing. This role ensures cGMP compliance data integrity safety and r
Position OverviewThe Supervisor QC Microbiology leads a team of microbiology analysts to execute GMP testing environmental monitoring and microbiological control programs supporting clinical and/or commercial manufacturing. This role ensures cGMP compliance data integrity safety and r
Position OverviewThe Supervisor QC Microbiology leads a team of microbiology analysts to execute GMP testing environmental monitoring and microbiological control programs supporting clinical and/or commercial manufacturing. This role ensures cGMP compliance data integrity safety and r
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Position OverviewThis role will apply principles and techniques of mechanical engineering for the design and development of mechanical equipment and sub-systems including concept development specification of mechanical loads component selection materials of construction and tolerances
Position OverviewThis role will apply principles and techniques of mechanical engineering for the design and development of mechanical equipment and sub-systems including concept development specification of mechanical loads component selection materials of construction and tolerances
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Position OverviewPosition Description We are hiring a Product Specialist II. The Product Specialist II will support custom business function for on-boarding new products and/or new site qualification. They will manage the qualification of new raw materials such as new chemicals and/or
Position OverviewPosition Description We are hiring a Product Specialist II. The Product Specialist II will support custom business function for on-boarding new products and/or new site qualification. They will manage the qualification of new raw materials such as new chemicals and/or
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Position OverviewFUJIFILM Cellular Dynamics Inc. is seeking an expert in validation engineering who will apply knowledge of qualification and validation principles to manufacturing processes quality systems engineering design fundamentals regulatory authority expectations and industry
Position OverviewFUJIFILM Cellular Dynamics Inc. is seeking an expert in validation engineering who will apply knowledge of qualification and validation principles to manufacturing processes quality systems engineering design fundamentals regulatory authority expectations and industry
Position OverviewFUJIFILM Cellular Dynamics Inc. is seeking an Associate Director Program Design to lead the scoping design and proposal development process for new CDMO business opportunities from client request for proposal through contract signature. This individual contributor rol
Position OverviewFUJIFILM Cellular Dynamics Inc. is seeking an Associate Director Program Design to lead the scoping design and proposal development process for new CDMO business opportunities from client request for proposal through contract signature. This individual contributor rol
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Position OverviewThe QA Engineer Validation is responsible for helping to drive the Quality oversight for commissioning and qualification processes. This role is responsible for quality assurance oversight review and approval of validation activities and documents associated with new
Position OverviewThe QA Engineer Validation is responsible for helping to drive the Quality oversight for commissioning and qualification processes. This role is responsible for quality assurance oversight review and approval of validation activities and documents associated with new
Position OverviewThe Scientist 1 QC Analytical Development Chemistry supports the transfer of analytical Chemistry methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Holly Springs. This ro
Position OverviewThe Scientist 1 QC Analytical Development Chemistry supports the transfer of analytical Chemistry methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Holly Springs. This ro
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Position OverviewShape the learning backbone by leading cross-site improvements system updates and migration to nextgen LMS. Setting standards for content structure configuration and reportingwhile supporting sites with structure data insights and Q&A. Partner with the Learning Global
Position OverviewShape the learning backbone by leading cross-site improvements system updates and migration to nextgen LMS. Setting standards for content structure configuration and reportingwhile supporting sites with structure data insights and Q&A. Partner with the Learning Global
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Position OverviewThe Scientist 1 QC Compendial Testing participates in the Technology Transfer (TT) of material methods into the FUJIFILM Biotechnologies Holly Springs Quality Control Laboratory with limited supervision. This includes the onboarding of new and generic raw materials as
Position OverviewThe Scientist 1 QC Compendial Testing participates in the Technology Transfer (TT) of material methods into the FUJIFILM Biotechnologies Holly Springs Quality Control Laboratory with limited supervision. This includes the onboarding of new and generic raw materials as
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Position Overview FUJIFILM Electronic Materials U.S.A. Inc. is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa AZ facility for a Talent Acquisition Specialist! The Role Taking direction
Position Overview FUJIFILM Electronic Materials U.S.A. Inc. is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa AZ facility for a Talent Acquisition Specialist! The Role Taking direction
Position OverviewThe Senior Analyst 1 QC Compendial Testing ensures laboratory operations are Good Manufacturing Practices (GMP)-compliant according to United States/Europe/Japan (USP/EP/JP) regulations. The role participates in the Technology Transfer (TT) of established methods into
Position OverviewThe Senior Analyst 1 QC Compendial Testing ensures laboratory operations are Good Manufacturing Practices (GMP)-compliant according to United States/Europe/Japan (USP/EP/JP) regulations. The role participates in the Technology Transfer (TT) of established methods into
Position OverviewThe Senior Analyst 1 QC Compendial Testing ensures laboratory operations are Good Manufacturing Practices (GMP)-compliant according to United States/Europe/Japan (USP/EP/JP) regulations. The role participates in the Technology Transfer (TT) of established methods into
Position OverviewThe Senior Analyst 1 QC Compendial Testing ensures laboratory operations are Good Manufacturing Practices (GMP)-compliant according to United States/Europe/Japan (USP/EP/JP) regulations. The role participates in the Technology Transfer (TT) of established methods into