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fluxus
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EncryptedSite is Encrypted
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CountryHosted in United States
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Traffic rank#985,452 Site Rank
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Site age29 yrs old
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Site Owner informationWhois info
Website is Safe
Traffic rank
#985,452
#985,452
Site age
29 yrs
29 yrs
Location
United States
United States
Newest job postings for fluxus
via Lever
schedule_type: Full-time
To support its product development activities, Fluxus Inc. is seeking a highly motivated, interdisciplinary, product development research associate / technician / engineer with relevant, hands-on experience. She/He/They will be part of the System Integration team and will play a vital role in developing, testing, optimizing, and troubleshooting many aspects related to a novel diagnostics... technology platform.
She/He/They will work closely with
To support its product development activities, Fluxus Inc. is seeking a highly motivated, interdisciplinary, product development research associate / technician / engineer with relevant, hands-on experience. She/He/They will be part of the System Integration team and will play a vital role in developing, testing, optimizing, and troubleshooting many aspects related to a novel diagnostics... technology platform.
She/He/They will work closely with other Fluxus teams and will perform instrument development tasks related to novel detection systems, complex fluidic systems and assay optimization on prototypes and automated systems. Activities will involve amongst others the testing, development and optimization of functional biochips, fluidic cartridges, and analytical instruments. The successful applicant will work within a multidisciplinary team of engineers, scientists and manufacturing personnel. Part of the activities might be conducted in a BSL2 laboratory area and could involve the handling of human patient fluid samples. Other activities might be conducted in a CER (controlled environment) setting.
Principal Duties and Responsibilities
• Support diverse aspects related to the product development of biochip-based, optofluidic diagnostics platforms. Applies diversified knowledge of interdisciplinary knowledge to understand, test and optimize all aspects of the technology
• Development, optimization & testing of biochips, cartridges and instruments, in collaboration with other groups and external suppliers
• Provide support in preparing documentation
• Use Good Documentation Practices (GDP) while authoring Experimental summaries, DOPs, SOPs, batch records (BRs) and forms (FRs) for various unit operations
• Process development and optimization related to biomolecular sensing
• Support all aspects of technology transfer to and from development partners
• Develop, test and execute QC procedures
• Process troubleshooting to determine root cause and find possible engineering solutions
Requirements
• M.S. Degree in bio-, mechanical-, electrical- or chemical engineering, chemistry or biochemistry, or related, technical discipline, with 2+ years hands-on R&D or engineering or product development experience
• Inquisitive, interdisciplinary mindset
• Extensive, hands-on experience working with and optimizing complex instrumentation
• Excellent organizational as well as English (verbal and written) communication skills
• Experienced in using diverse instruments such as – or similar to e.g. – analytical instrumentation, DAQ interfaces, UV-VIS spectrometer, scanning electron microscope (SEM)
• Good knowledge of data analysis methods including good knowledge of statistics
• Self-starter, detail-oriented, motivated, thoughtful, and with a strong work ethic
• Ability and willingness to quickly learn and apply new skills, procedures and approaches
• Proven ability to work collaboratively in a team-based environment
• Proven ability to handle multiple competing priorities in a fast-paced work environment
• Candidates must be able to work in the US for any employer at this time
Other Beneficial Skill Sets
• Experience within an industrial product development environment
• Experience in working with chemicals and biochemical buffers and molecules
• Experience in process optimization using e.g. DOE and/or data acquisition and analysis systems
• Experience in building and operating automated and robotic systems
• Experience in industrial process verification and validation
About Fluxus
Fluxus Inc. is a privately held development-stage medical device company located in Santa Clara, CA, USA. The Company’s immediate focus is the development and commercialization of biochip-based detection platforms for ultra-high sensitivity diagnostics and bioanalytical applications. Our culture represents innovative, driven, and talented professionals with diverse perspectives, but one which is united on a mission to significantly and positively make a difference in healthcare.
As a member of Fluxus’ team, you would join an entrepreneurial and growing company that functions with the electricity of a startup but is led by a management team with a proven success record of 25+ years in life science tools and diagnostics. We look forward to hearing from you to learn more about your expertise and career goals. Fluxus provides a competitive benefits package and is an Equal Opportunity Employer regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law Show more details...
She/He/They will work closely with other Fluxus teams and will perform instrument development tasks related to novel detection systems, complex fluidic systems and assay optimization on prototypes and automated systems. Activities will involve amongst others the testing, development and optimization of functional biochips, fluidic cartridges, and analytical instruments. The successful applicant will work within a multidisciplinary team of engineers, scientists and manufacturing personnel. Part of the activities might be conducted in a BSL2 laboratory area and could involve the handling of human patient fluid samples. Other activities might be conducted in a CER (controlled environment) setting.
Principal Duties and Responsibilities
• Support diverse aspects related to the product development of biochip-based, optofluidic diagnostics platforms. Applies diversified knowledge of interdisciplinary knowledge to understand, test and optimize all aspects of the technology
• Development, optimization & testing of biochips, cartridges and instruments, in collaboration with other groups and external suppliers
• Provide support in preparing documentation
• Use Good Documentation Practices (GDP) while authoring Experimental summaries, DOPs, SOPs, batch records (BRs) and forms (FRs) for various unit operations
• Process development and optimization related to biomolecular sensing
• Support all aspects of technology transfer to and from development partners
• Develop, test and execute QC procedures
• Process troubleshooting to determine root cause and find possible engineering solutions
Requirements
• M.S. Degree in bio-, mechanical-, electrical- or chemical engineering, chemistry or biochemistry, or related, technical discipline, with 2+ years hands-on R&D or engineering or product development experience
• Inquisitive, interdisciplinary mindset
• Extensive, hands-on experience working with and optimizing complex instrumentation
• Excellent organizational as well as English (verbal and written) communication skills
• Experienced in using diverse instruments such as – or similar to e.g. – analytical instrumentation, DAQ interfaces, UV-VIS spectrometer, scanning electron microscope (SEM)
• Good knowledge of data analysis methods including good knowledge of statistics
• Self-starter, detail-oriented, motivated, thoughtful, and with a strong work ethic
• Ability and willingness to quickly learn and apply new skills, procedures and approaches
• Proven ability to work collaboratively in a team-based environment
• Proven ability to handle multiple competing priorities in a fast-paced work environment
• Candidates must be able to work in the US for any employer at this time
Other Beneficial Skill Sets
• Experience within an industrial product development environment
• Experience in working with chemicals and biochemical buffers and molecules
• Experience in process optimization using e.g. DOE and/or data acquisition and analysis systems
• Experience in building and operating automated and robotic systems
• Experience in industrial process verification and validation
About Fluxus
Fluxus Inc. is a privately held development-stage medical device company located in Santa Clara, CA, USA. The Company’s immediate focus is the development and commercialization of biochip-based detection platforms for ultra-high sensitivity diagnostics and bioanalytical applications. Our culture represents innovative, driven, and talented professionals with diverse perspectives, but one which is united on a mission to significantly and positively make a difference in healthcare.
As a member of Fluxus’ team, you would join an entrepreneurial and growing company that functions with the electricity of a startup but is led by a management team with a proven success record of 25+ years in life science tools and diagnostics. We look forward to hearing from you to learn more about your expertise and career goals. Fluxus provides a competitive benefits package and is an Equal Opportunity Employer regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law Show more details...
via SquarePeg Hires
posted_at: 5 days agoschedule_type: Full-time
To support its life science tool and diagnostics product development, Fluxus Inc. is seeking a highly motivated, interdisciplinary software engineer with relevant, hands-on experience and proven track record of innovative engineering at the intersection of software and hardware development. She/He will be part of Fluxus’ product development team and work closely with other teams to design... develop, and implement a rowing suite of bioanalytical
To support its life science tool and diagnostics product development, Fluxus Inc. is seeking a highly motivated, interdisciplinary software engineer with relevant, hands-on experience and proven track record of innovative engineering at the intersection of software and hardware development. She/He will be part of Fluxus’ product development team and work closely with other teams to design... develop, and implement a rowing suite of bioanalytical solutions comprised of integrated biochips, proprietary reagents, and custom instrumentation. The position will involve a variety of activities related to the design, control, and interfacing of various electronic and data analysis systems. Development of single-molecule detection technology will involve optoelectronic signal integration and programmatic/hardware data analysis. The successful applicant will work within multidisciplinary teams of engineers, scientists, and manufacturing specialists.
Responsibilities
• Lead/Support diverse aspects of software and UI development related to the development of novel, diagnostic instrument platforms
• Develop control/analysis software for RUO (Research Use Only) and FDA regulated instrumentation
• Contribute to a custom user interface for scientific and medical diagnostic systems
• Work with external software/hardware engineers towards fulfilment of Fluxus’ software goals (collaborate, peer review, architect and oversee execution)
• Support all aspects of technology transfer to and from internal and external partners.
Requirements
• Degree/Experience Requirements: B.S./M.S. with 3+ years of relevant experience
• Significant experience with instrument related software engineering using C# (or adjacent language)
• Significant experience with industry coding best practices (Git management, unit testing, documentation, etc.)
• Experience developing and supporting user interfaces
• Experience developing, implementing, consuming, and supporting contracted APIs
• Technical capabilities allowing interfacing with all vertical levels of contributors (i.e., engineer to CTO)
• Preferred Skill Sets
• Experience with firmware level interaction
• Experience with delivering quality conformant software (SaMD)
• Experience with Python programming
• Worked with frontend frameworks (React)
• Ability to develop custom equipment with external vendors and/or internal engineering resources
• Self-starter, detail-oriented, motivated, thoughtful, and with a strong work ethic Show more details...
Responsibilities
• Lead/Support diverse aspects of software and UI development related to the development of novel, diagnostic instrument platforms
• Develop control/analysis software for RUO (Research Use Only) and FDA regulated instrumentation
• Contribute to a custom user interface for scientific and medical diagnostic systems
• Work with external software/hardware engineers towards fulfilment of Fluxus’ software goals (collaborate, peer review, architect and oversee execution)
• Support all aspects of technology transfer to and from internal and external partners.
Requirements
• Degree/Experience Requirements: B.S./M.S. with 3+ years of relevant experience
• Significant experience with instrument related software engineering using C# (or adjacent language)
• Significant experience with industry coding best practices (Git management, unit testing, documentation, etc.)
• Experience developing and supporting user interfaces
• Experience developing, implementing, consuming, and supporting contracted APIs
• Technical capabilities allowing interfacing with all vertical levels of contributors (i.e., engineer to CTO)
• Preferred Skill Sets
• Experience with firmware level interaction
• Experience with delivering quality conformant software (SaMD)
• Experience with Python programming
• Worked with frontend frameworks (React)
• Ability to develop custom equipment with external vendors and/or internal engineering resources
• Self-starter, detail-oriented, motivated, thoughtful, and with a strong work ethic Show more details...
via SquarePeg
posted_at: 5 days agoschedule_type: Full-time
Fluxus Inc. is seeking a highly motivated and experienced individual to lead the manufacturing group, manufacturing process development/engineering as well as quality insurance related to the development and commercialization of a novel diagnostics platform.
She/He will work to maintain and provide continuous optimization in the manufacture of diagnostic cartridges involving biochips and plastic... consumables, including process development and supply
Fluxus Inc. is seeking a highly motivated and experienced individual to lead the manufacturing group, manufacturing process development/engineering as well as quality insurance related to the development and commercialization of a novel diagnostics platform.
She/He will work to maintain and provide continuous optimization in the manufacture of diagnostic cartridges involving biochips and plastic... consumables, including process development and supply chain management.
Together with Fluxus R&D teams, the candidate will also be involved in process transfer from R&D and manufacturing process optimization. The successful applicant will work within a multidisciplinary team of engineers, scientists and manufacturing personnel. Part of the activities might be conducted in a clean environment setting and/or in a BSL2 laboratory area involving handling of human patient fluid samples.
Fluxus, Inc. is an innovator in single-molecule detection and ultra-high sensitivity platforms based on its expertise in optofluidics, assay development, system integration and microsystem technologies. The Fluxus product development infrastructure and suite of proprietary technologies are ideally suited for the robust development of advanced diagnostic products.
Responsibilities
• Manage the Fluxus Manufacturing, Manufacturing Engineering and Quality teams
• Ensure supply meets demand and quality related to diagnostic consumables and systems
• Lead process development and engineering towards a stable and reliable manufacturing operation. Applies intensive and diversified knowledge of process optimization, engineering, design and optimization principles, and practices related to complex systems
• Responsible for supply chain management
• Develop, test and validate quality control tools, processes and procedures
• Provide support in the maintenance and optimization of the eQMS system
• Development, optimization, testing, sourcing and scale-up of biochips, cartridges and instruments, in collaboration with other groups and external suppliers
• Support in preparing documentation and managing external suppliers and engineering partners for regulatory submissions
• Use and develop Good Documentation Practices (GDP) while authoring DOPs, SOPs, batch records (BRs) and forms (FRs) for various unit operations
• Support all aspects of manufacturing technology transfer to and from development partners
• Interface with internal resources and external vendors to design, test and validate equipment
• Working knowledge of cGMPs, quality requirements for various regulatory agencies like FDA Certification is preferred
• Requirements
• BS or MS Degree in and engineering or related, technical discipline
• 7+ years of hands-on R&D and/or engineering and/or process/product development experience preferably in a biotechnology-related, industrial, product development/manufacturing environment.
• Interdisciplinary mindset
• Hands on experience with optimizing processes involving materials, micro-fluidics, reagents and electronics. Knowledge of DOE process optimization preferred.
• Hands-on experience in the development of processes related to e.g., precision plastic consumables, microfabrication and systems involving reagents and liquids.
• Good knowledge of data analysis methods / statistics.
• Ability to develop custom equipment by collaborating with external vendors or internal engineering resources.
• Experienced in cGMPs and operating under a QMS
• Experienced in verification and validation of instruments and processes.
• Self-starter, detail-oriented, motivated, thoughtful, and with a strong work ethic.
• Excellent organizational as well as English verbal and written communication skills.
• Ability and willingness to quickly learn and apply new skills, procedures, and approaches.
• Proven ability to work collaboratively in a team-based environment.
• Proven ability to handle multiple competing priorities in a fast-paced work environment.
• Other Beneficial Skill Sets
• Experience in CAD design
• Knowledge of medical device and quality system regulations and standards (i.e., FDA QSR,ISO13485)
• Experience in industrial process verification and validation Show more details...
She/He will work to maintain and provide continuous optimization in the manufacture of diagnostic cartridges involving biochips and plastic... consumables, including process development and supply chain management.
Together with Fluxus R&D teams, the candidate will also be involved in process transfer from R&D and manufacturing process optimization. The successful applicant will work within a multidisciplinary team of engineers, scientists and manufacturing personnel. Part of the activities might be conducted in a clean environment setting and/or in a BSL2 laboratory area involving handling of human patient fluid samples.
Fluxus, Inc. is an innovator in single-molecule detection and ultra-high sensitivity platforms based on its expertise in optofluidics, assay development, system integration and microsystem technologies. The Fluxus product development infrastructure and suite of proprietary technologies are ideally suited for the robust development of advanced diagnostic products.
Responsibilities
• Manage the Fluxus Manufacturing, Manufacturing Engineering and Quality teams
• Ensure supply meets demand and quality related to diagnostic consumables and systems
• Lead process development and engineering towards a stable and reliable manufacturing operation. Applies intensive and diversified knowledge of process optimization, engineering, design and optimization principles, and practices related to complex systems
• Responsible for supply chain management
• Develop, test and validate quality control tools, processes and procedures
• Provide support in the maintenance and optimization of the eQMS system
• Development, optimization, testing, sourcing and scale-up of biochips, cartridges and instruments, in collaboration with other groups and external suppliers
• Support in preparing documentation and managing external suppliers and engineering partners for regulatory submissions
• Use and develop Good Documentation Practices (GDP) while authoring DOPs, SOPs, batch records (BRs) and forms (FRs) for various unit operations
• Support all aspects of manufacturing technology transfer to and from development partners
• Interface with internal resources and external vendors to design, test and validate equipment
• Working knowledge of cGMPs, quality requirements for various regulatory agencies like FDA Certification is preferred
• Requirements
• BS or MS Degree in and engineering or related, technical discipline
• 7+ years of hands-on R&D and/or engineering and/or process/product development experience preferably in a biotechnology-related, industrial, product development/manufacturing environment.
• Interdisciplinary mindset
• Hands on experience with optimizing processes involving materials, micro-fluidics, reagents and electronics. Knowledge of DOE process optimization preferred.
• Hands-on experience in the development of processes related to e.g., precision plastic consumables, microfabrication and systems involving reagents and liquids.
• Good knowledge of data analysis methods / statistics.
• Ability to develop custom equipment by collaborating with external vendors or internal engineering resources.
• Experienced in cGMPs and operating under a QMS
• Experienced in verification and validation of instruments and processes.
• Self-starter, detail-oriented, motivated, thoughtful, and with a strong work ethic.
• Excellent organizational as well as English verbal and written communication skills.
• Ability and willingness to quickly learn and apply new skills, procedures, and approaches.
• Proven ability to work collaboratively in a team-based environment.
• Proven ability to handle multiple competing priorities in a fast-paced work environment.
• Other Beneficial Skill Sets
• Experience in CAD design
• Knowledge of medical device and quality system regulations and standards (i.e., FDA QSR,ISO13485)
• Experience in industrial process verification and validation Show more details...
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