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Biochemist for MedTech start-up

We are looking for a Biochemist who will partly support our laboratory work in the development of new IVD devices in close collaboration with the R&D team. And partly be able to perform biochemistry production and QC work in our production unit. Furthermore, you will work according to our Quality Management System and be part of delivering our high-quality products already in demand in the market.

Your responsibilities

  • Work according to BluSense ISO13485 quality system
  • Production: Being operator/reviewer of Biochemistry production (including production and QC) for IVD products developed by BluSense
  • Writing and reviewing production procedures and specifications for new and existing IVD products
  • R&D: Preparation (executing and recording) of materials (such as buffers, reagents, controls) for development and verification of IVD products, following BSD procedures for traceability and lab safety
  • R&D: Assist executing and reporting laboratory experiments (such as BluSense reader assay testing), following BSD procedures for traceability and lab safety
  • Execute laboratory work in Biochemistry, Biological Safety Level 2 and 3 labs


Qualifications

You are a highly skilled and dedicated biochemist who likes challenges and thrives in a busy and dynamic work environment. You can handle multiple tasks at the same time while consistently delivering high-quality results. You can work independently and at the same time be part of a team.
You can follow guidelines from R&D scientists and implement protocols by yourself.   

Specific qualifications and skills

  • B.Sc. or M.Sc. in Biotechnology, Biochemistry, Biomedical Engineering or Chemistry.
  • Experience with standard biotech laboratory techniques such as ph-meter, microbalance, sonication, pipetting and centrifugation
  • Knowledge of ISO:13485 (within research and production) would be an advantage
  • Knowledge of IVD is an advantage
  • Speaks and understands English
  • Solid computer literacy, including Microsoft Office (especially Microsoft Excel)
  • Work experience in a team-oriented environment


Skills and Abilities

  • Structured and ability to keep a clear overview
  • Working independently with a focus on documentation and traceability
  • Curious and proactively reaching out for knowledge
  • Ability to organize and conduct experiments
  • Aptitude to run repetitive protocols while constantly monitoring important details
  • Ability to monitor and troubleshoot technical issues with custom electronic instruments
  • Able to maintain focus in a fast-paced and dynamic environment
  • Excellent interpersonal skills to communicate effectively with colleagues
  • Positive attitude and open-minded
  • A good team player
  • Commitment to the team’s goal of providing outstanding technical support for a research project
  • Motivated and dedicated to lab work
  • Keen interest in emerging technologies


We offer

  • A challenging and very dynamic working environment as part of the start up community at Symbion Science Park
  • Working in a MedTech start up – making a difference to a large part of the world’s population
  • A possibility to contribute to the constant growth of R&D and production
  • Co-operation and exchange of ideas within a multinational and interdisciplinary team
  • Professional and personal development in being part of scaling up production operations
  • Good location easily reachable by S-train and parking space for free
  • Good coffee and possibility to buy lunch in the canteen


How to apply

We will process applications as they arrive. Therefore, please apply not later than April 28th, by sending us your CV and a cover letter via thehub.dk. Qualified applicants can expect to be called for an interview before the deadline.


We plan to hire for a job start in May/June 2019.

Please reach out to Mattias Parmvi, Biochemistry Manager (Mattias.Parmvi@blusense-diagnostics.com)

 

About BluSense

BluSense Diagnostics is an innovative start up in the MedTech business! We work hard to become global leader within the Infectious disease point-of-care diagnostics. We combine complex scientific areas such as nanotechnology, molecular biology, biochemistry, optics, and hardware and software engineering in developing the next generation of point-of-care testing for infectious mosquito-borne diseases.


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330008007Phoenix-87ea60e912019-04-15T00:00:00Biochemist for MedTech start-up

We are looking for a Biochemist who will partly support our laboratory work in the development of new IVD devices in close collaboration with the R&D team. And partly be able to perform biochemistry production and QC work in our production unit. Furthermore, you will work according to our Quality Management System and be part of delivering our high-quality products already in demand in the market.

Your responsibilities

  • Work according to BluSense ISO13485 quality system
  • Production: Being operator/reviewer of Biochemistry production (including production and QC) for IVD products developed by BluSense
  • Writing and reviewing production procedures and specifications for new and existing IVD products
  • R&D: Preparation (executing and recording) of materials (such as buffers, reagents, controls) for development and verification of IVD products, following BSD procedures for traceability and lab safety
  • R&D: Assist executing and reporting laboratory experiments (such as BluSense reader assay testing), following BSD procedures for traceability and lab safety
  • Execute laboratory work in Biochemistry, Biological Safety Level 2 and 3 labs


Qualifications

You are a highly skilled and dedicated biochemist who likes challenges and thrives in a busy and dynamic work environment. You can handle multiple tasks at the same time while consistently delivering high-quality results. You can work independently and at the same time be part of a team.
You can follow guidelines from R&D scientists and implement protocols by yourself.   

Specific qualifications and skills

  • B.Sc. or M.Sc. in Biotechnology, Biochemistry, Biomedical Engineering or Chemistry.
  • Experience with standard biotech laboratory techniques such as ph-meter, microbalance, sonication, pipetting and centrifugation
  • Knowledge of ISO:13485 (within research and production) would be an advantage
  • Knowledge of IVD is an advantage
  • Speaks and understands English
  • Solid computer literacy, including Microsoft Office (especially Microsoft Excel)
  • Work experience in a team-oriented environment


Skills and Abilities

  • Structured and ability to keep a clear overview
  • Working independently with a focus on documentation and traceability
  • Curious and proactively reaching out for knowledge
  • Ability to organize and conduct experiments
  • Aptitude to run repetitive protocols while constantly monitoring important details
  • Ability to monitor and troubleshoot technical issues with custom electronic instruments
  • Able to maintain focus in a fast-paced and dynamic environment
  • Excellent interpersonal skills to communicate effectively with colleagues
  • Positive attitude and open-minded
  • A good team player
  • Commitment to the team’s goal of providing outstanding technical support for a research project
  • Motivated and dedicated to lab work
  • Keen interest in emerging technologies


We offer

  • A challenging and very dynamic working environment as part of the start up community at Symbion Science Park
  • Working in a MedTech start up – making a difference to a large part of the world’s population
  • A possibility to contribute to the constant growth of R&D and production
  • Co-operation and exchange of ideas within a multinational and interdisciplinary team
  • Professional and personal development in being part of scaling up production operations
  • Good location easily reachable by S-train and parking space for free
  • Good coffee and possibility to buy lunch in the canteen


How to apply

We will process applications as they arrive. Therefore, please apply not later than April 28th, by sending us your CV and a cover letter via thehub.dk. Qualified applicants can expect to be called for an interview before the deadline.


We plan to hire for a job start in May/June 2019.

Please reach out to Mattias Parmvi, Biochemistry Manager (Mattias.Parmvi@blusense-diagnostics.com)

 

About BluSense

BluSense Diagnostics is an innovative start up in the MedTech business! We work hard to become global leader within the Infectious disease point-of-care diagnostics. We combine complex scientific areas such as nanotechnology, molecular biology, biochemistry, optics, and hardware and software engineering in developing the next generation of point-of-care testing for infectious mosquito-borne diseases.

2019-06-11T00:52:07.033 We are looking for a Biochemist who will partly support our laboratory work in the development of new IVD devices in close collaboration with the R D team. And partly be able to perform biochemistry production and QC work in our production unit. Furthermore, you will work according to our Quality Management System and be part of delivering our high-quality products already in demand in the market. Your responsibilities Work according to BluSense ISO13485 quality system Production: Being operator reviewer of Biochemistry production (including production and QC) for IVD products developed by BluSense Writing and reviewing production procedures and specifications for new and existing IVD products R D: Preparation (executing and recording) of materials (such as buffers, reagents, controls) for development and verification of IVD products, following BSD procedures for traceability and lab safety R D: Assist executing and reporting laboratory experiments (such as BluSense reader assay testing), following BSD procedures for traceability and lab safety Execute laboratory work in Biochemistry, Biological Safety Level 2 and 3 labs Qualifications You are a highly skilled and dedicated biochemist who likes challenges and thrives in a busy and dynamic work environment. You can handle multiple tasks at the same time while consistently delivering high-quality results. You can work independently and at the same time be part of a team. You can follow guidelines from R D scientists and implement protocols by yourself. Specific qualifications and skills B.Sc. or M.Sc. in Biotechnology, Biochemistry, Biomedical Engineering or Chemistry. Experience with standard biotech laboratory techniques such as ph-meter, microbalance, sonication, pipetting and centrifugation Knowledge of ISO:13485 (within research and production) would be an advantage Knowledge of IVD is an advantage Speaks and understands English Solid computer literacy, including Microsoft Office (especially Microsoft Excel) Work experience in a team-oriented environment Skills and Abilities Structured and ability to keep a clear overview Working independently with a focus on documentation and traceability Curious and proactively reaching out for knowledge Ability to organize and conduct experiments Aptitude to run repetitive protocols while constantly monitoring important details Ability to monitor and troubleshoot technical issues with custom electronic instruments Able to maintain focus in a fast-paced and dynamic environment Excellent interpersonal skills to communicate effectively with colleagues Positive attitude and open-minded A good team player Commitment to the team s goal of providing outstanding technical support for a research project Motivated and dedicated to lab work Keen interest in emerging technologies We offer A challenging and very dynamic working environment as part of the start up community at Symbion Science Park Working in a MedTech start up making a difference to a large part of the world s population A possibility to contribute to the constant growth of R D and production Co-operation and exchange of ideas within a multinational and interdisciplinary team Professional and personal development in being part of scaling up production operations Good location easily reachable by S-train and parking space for free Good coffee and possibility to buy lunch in the canteen How to apply We will process applications as they arrive. Therefore, please apply not later than April 28th, by sending us your CV and a cover letter via thehub.dk. Qualified applicants can expect to be called for an interview before the deadline. We plan to hire for a job start in May June 2019. Please reach out to Mattias Parmvi, Biochemistry Manager (Mattias.Parmvi@blusense-diagnostics.com) About BluSense BluSense Diagnostics is an innovative start up in the MedTech business! We work hard to become global leader within the Infectious disease point-of-care diagnostics. We combine complex scientific areas such as nanotechnology, molecular biology, biochemistry, optics, and hardware and software engineering in developing the next generation of point-of-care testing for infectious mosquito-borne diseases.11jobnet87ea60e9100000000000IDK_OFIR_02DKDanmark228DKK2019-06-10T00:00:000000https://thehub.dk/jobs/biochemist-for-medtech-start-up0EuropaDanmarkSjælland & øerStorkøbenhavnKøbenhavn3509306BLUSENSE DIAGNOSTICS APS11Fruebjergvej 32100København ØDKDanmark0DKDanmarkDKDanmark8Fuldtid46Permanent746208JobNet4975829497582910015-04-20190https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=87ea60e9https://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=87ea60e9https://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=87ea60e9&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=87ea60e9&page=EmailApplyForm&component=SendApplicationButton1Dansk3Læse/ tale311105Laborant20Ingeniør og naturvidenskab361482991Zydrunezydrune.domarkaite@blusense-diagnostics.comDKDanmarkDKDanmark330075334ScanPeople søger en Laborant til Xellia PharmaceuticalsRobot ScanPeople søger en laborant til længerevarende vikariat hos Xellia Pharmaceuticals - en spændende og international virksomhed, beliggende i København. Virksomheden er ejet af Novo Holdings A S, og beskæftiger mere end 1.500 medarbejdere globalt. Arbejdsopgaver Kemiske analyser: Kemiske analyser (HPLC, GC, IC). Databehandling og afrapportering af resultater i LIMS (Laboratory Information Management System). Kontrol og vedligehold af laboratorieudstyr. Deltagelse i løsning af problemstillinger i afdelingen og API-produktionen. Validering af metoder og kalibrering samt kvalificering af udstyr. Kvalifikationer: Du er uddannet laborant, kemiingeniør eller tilsvarende - og brænder for dit arbejde. Du har flere års erfaring med at arbejde under GMP-forhold og compliance. Du har gerne erfaring med lægemiddelproduktion. Du har solid erfaring inden for kemiske analyser. Du har en ansvarlighed for dit arbejde - og stolthed i at aflevere dine opgaver inden for aftalt deadline. Du er fleksibel og kan arbejde både selvstændigt og i teams. Du møder glad på arbejde, og har et smittende humør. Opstart Hurtigst muligt, men vi venter på den rette. Vi indkalder løbende til samtaler, så send hellere din ansøgning i dag end i morgen. Ansøgning Finder du ovenstående lige så spændende som os, og er du klar til nye udfordringer, skal du via nedenstående link indtaste dine oplysninger og uploade ansøgning og CV. Har du nogle spørgsmål til stillingen, kan du kontakte Liselotte Schwanenflügel Jensen på 43 31 00 71. Søg stillingen her:http: www.scanpeople.axp.dk index.php?axp_act adetails version 1 axp_recruitment_references[] 10288OBS: Hvis du allerede har registreret dig via vores database, skal du blot logge ind og tilføje jobkoden 10288 for at søge jobbet. Vi ser frem til at modtage din ansøgning! Om Xellia Pharmaceuticals Xellia Pharmaceuticals har mere end 1.500 medarbejdere globalt. Hovedkontoret er i København og virksomheden er ejet af Novo Holdings A S. Xellia har topmoderne, producerende fabrikker i USA, Kina, Danmark og Ungarn samt udviklingsfabrikker i Norge og Kroatien. Virksomheden udmærker sig ved deres innovative produktudvikling samt produkter af høj kvalitet. Læs mere om Xellia her: http: www.xellia.com Om ScanPeople: ScanPeople er en solid og dynamisk, danskejet virksomhed i Scanavo gruppen. En af ScanPeoples store styrker er medarbejdernes meget forskelligartede baggrunde. Vores succes som servicevirksomhed afhænger af et godt og effektivt samspil mellem os, vores kunder og vores kandidater. Vi besidder et vidtrækkende netværk og suppleret med en god solid teoretisk og praktisk baggrund, sikrer vi den bedste service og kvalitet til alle vi er i berøring med. Vi er yderst servicemindede og kompetente rådgivere med en bred erfaring indenfor vikarassistance, search, rekruttering, interim management og outplacement. Vi har med ScanPeoples blå division specialiseret os i at levere personale indenfor Industri, Medico, Teknik og Pharma. Vi har med ScanPeoples grønne division specialiseret os i at levere personale indenfor Salg, Marketing, Kontor og Administration. Yderligere information findes på: www.scanpeople.dk

ScanPeople søger en laborant til længerevarende vikariat hos Xellia Pharmaceuticals - en spændende og international virksomhed, beliggende i København. Virksomheden er ejet af Novo Holdings A/S, og beskæftiger mere end 1.500 medarbejdere globalt.  

Arbejdsopgaver – Kemiske analyser:

  • Kemiske analyser (HPLC, GC, IC).
  • Databehandling og afrapportering af resultater i LIMS (Laboratory Information Management System).
  • Kontrol og vedligehold af laboratorieudstyr.
  • Deltagelse i løsning af problemstillinger i afdelingen og API-produktionen.
  • Validering af metoder og kalibrering samt kvalificering af udstyr.

Kvalifikationer:  

  • Du er uddannet laborant, kemiingeniør eller tilsvarende - og brænder for dit arbejde.
  • Du har flere års erfaring med at arbejde under GMP-forhold og compliance.
  • Du har gerne erfaring med lægemiddelproduktion.
  • Du har solid erfaring inden for kemiske analyser.
  • Du har en ansvarlighed for dit arbejde - og stolthed i at aflevere dine opgaver inden for aftalt deadline.
  • Du er fleksibel og kan arbejde både selvstændigt og i teams.
  • Du møder glad på arbejde, og har et smittende humør.

Opstart Hurtigst muligt, men vi venter på den rette. Vi indkalder løbende til samtaler, så send hellere din ansøgning i dag end i morgen.

Ansøgning Finder du ovenstående lige så spændende som os, og er du klar til nye udfordringer, skal du via nedenstående link

indtaste dine oplysninger og uploade ansøgning og CV.

Har du nogle spørgsmål til stillingen, kan du kontakte Liselotte Schwanenflügel Jensen på 43 31 00 71.

Søg stillingen her:http://www.scanpeople.axp.dk/index.php?axp_act=adetails&version=1&axp_recruitment_references[]=10288OBS: Hvis du allerede har registreret dig via vores database, skal du blot logge ind og tilføje jobkoden 10288 for at søge jobbet.

Vi ser frem til at modtage din ansøgning!

Om Xellia Pharmaceuticals Xellia Pharmaceuticals har mere end 1.500 medarbejdere globalt. Hovedkontoret er i København og virksomheden er ejet af Novo Holdings A/S. Xellia har topmoderne, producerende fabrikker i USA, Kina, Danmark og Ungarn samt udviklingsfabrikker i Norge og Kroatien. Virksomheden udmærker sig ved deres innovative produktudvikling samt produkter af høj kvalitet. Læs mere om Xellia her: http://www.xellia.com/ Om ScanPeople: ScanPeople er en solid og dynamisk, danskejet virksomhed i Scanavo gruppen. En af ScanPeoples store styrker er medarbejdernes meget forskelligartede baggrunde. Vores succes som servicevirksomhed afhænger af et godt og effektivt samspil mellem os, vores kunder og vores kandidater.

Vi besidder et vidtrækkende netværk og suppleret med en god solid teoretisk og praktisk baggrund, sikrer vi den bedste service og kvalitet til alle vi er i berøring med.

Vi er yderst servicemindede og kompetente rådgivere med en bred erfaring indenfor vikarassistance, search, rekruttering, interim management og outplacement.

Vi har med ScanPeoples blå division specialiseret os i at levere personale indenfor Industri, Medico, Teknik og Pharma.

Vi har med ScanPeoples grønne division specialiseret os i at levere personale indenfor Salg, Marketing, Kontor og Administration. Yderligere information findes på: www.scanpeople.dk

SCANPEOPLE ApSKøbenhavn S2019-08-19T00:00:002019-08-28T00:00:00
330075439SALT LABORATORY MANAGERRobot ABOUT SEABORG Seaborg Technologies is a start-up on the forefront of advanced and innovative nuclear reactor technology working to provide abundant, affordable and sustainable energy to the world. We have grown to become the leading molten salt reactor start-up outside of North America with an international team of 20 employees from four continents. We are actively developing the design for our Compact Molten Salt Reactor, alongside licensing and experimental validation activities of key safety and performance claims, and are currently planning a multi-million salt lab to accelerate these efforts. We are engaged with multiple stakeholders in the growing advanced reactor supply chain, primarily in East Asia. Our success is entirely due to our brilliant and passionate team of employees and experienced advisers - a team we are currently in the process of expanding with more world-class talent determined to create positive change in the world. THE ROLE We are hiring a laboratory manager to plan, procure equipment for, set up and run a state-of-the-art molten salt laboratory. The successful candidate will hold a senior position in our chemistry group, and will be supervising and performing experimental investigations of chemistry and materials properties in molten salts at high temperatures. Key words include laboratory planning and design, costing and scheduling, project management, procurement, safety management, supply chain management, radiation protection supervision, radioisotope tracking and inventory, quality assurance, equipment maintenance, and apparatus design. As a member of the reactor research and development team, the position will include collaboration with the reactor physics and engineering groups in Seaborg to ensure due consideration of important physical phenomena and safety considerations across all relevant disciplines. Some international travelling should be expected. RESPONSIBILITIES Seaborg employees must be able to act proactively and independently to perform a wide variety of functions that do not always correlate with experience or expertise (such as writing job advertisements). That being said, the advertised position is expected to include at least some of the following responsibilities and tasks:?? Plan, design and establish a state-of-the-art molten salt laboratory Budget costs of equipment, maintenance, running costs, consumables, etc. Procure, install and commission laboratory equipment Manage and maintain apparatus Develop, implement and enforce laboratory requirements and guidelines for quality assurance and occupational health and safety, in accordance with regional and company standards Aid the planning and execution of experimental campaigns to establish and validate chemical and materials properties in high-temperature molten salts Analyse and report findings to steer design activities Support the development of robust instrumentation and control systems for monitoring and controlling the chemistry, temperature and flow of molten salts, as well as for safeguards purposes Support IP development and acquisition activities Pursue compliance with regulatory requirements, including working to establish suitable standards and codes for the classification of salt-bearing systems, structures and components Design and develop methods to produce and purify salts Design and develop methods to perform and validate a wide range of measurements in molten salts, incl. of thermophysical properties, speciation, solubility, corrosion, heat transfer, turbulence, structural material properties, and more. REQUIREMENTS Desire to positively change the world by shaping the energy landscape of tomorrow Demonstrated ability to diligently approach and solve challenging tasks within time and budgetary constraints BSc or higher in chemistry, chemical engineering, materials science and engineering, or similar Considerable experience with setting up and or managing a chemical laboratory Prior experience with planning, scheduling, costing and procuring scientific equipment and effectively setting up and managing appropriate supply chains Demonstrated practical skills for developing and installing scientific equipment Experience developing and or working under effective quality assurance and operational health and safety systems in a chemical laboratory environment Experience working with molten salts, or other high-temperature and or corrosive fluids preferred Experience from nuclear industry preferred Team player with effective communication and interpersonal skills, including fluency in English Ability to travel by plane and communicate outside of normal working hours when necessary. At Seaborg we strongly value the combination of relevant experience, talent and personality traits that align with our team and overarching vision for a sustainable future. We therefore encourage applications from diverse backgrounds and are prepared to mould the job description to accommodate well-aligned candidates. OUR OFFER While our team is still small, our ambitions are not. Becoming a part of Seaborg presents a unique possibility to importantly impact and define the global energy landscape of tomorrow. We know that new ideas and influences are key to challenge the status quo and strive for continuous improvement, and so new hires can expect to importantly contribute to shaping both the technology and the future of the company.? We want to play an active role in enabling the personal and professional development of all employees so that they can evolve and grow to take on changing tasks and responsibilities. To give room for this development, we practice high work flexibility in an informal, merit-based environment without strict hierarchies. With time, we expect every employee to become an invaluable part of Seaborg and our success, and we underpin this expectation by offering all new employees stock options in the company. We are based in Denmark, a country known for its high quality of life and extensive social welfare system. That means free health care and education, generous vacation arrangements, progressive maternity and paternity leave provisions, etc. More on this at lifeindenmark.borger.dk. Our office is situated centrally in Copenhagen - a young and vibrant European capital on the Øresund coast with a thriving expat community and world-leading bicycle infrastructure.

ABOUT SEABORG

Seaborg Technologies is a start-up on the forefront of advanced and innovative nuclear reactor technology working to provide abundant, affordable and sustainable energy to the world. We have grown to become the leading molten salt reactor start-up outside of North America with an international team of 20 employees from four continents. We are actively developing the design for our Compact Molten Salt Reactor, alongside licensing and experimental validation activities of key safety and performance claims, and are currently planning a multi-million salt lab to accelerate these efforts. We are engaged with multiple stakeholders in the growing advanced reactor supply chain, primarily in East Asia. 

Our success is entirely due to our brilliant and passionate team of employees and experienced advisers - a team we are currently in the process of expanding with more world-class talent determined to create positive change in the world.

THE ROLE

We are hiring a laboratory manager to plan, procure equipment for, set up and run a state-of-the-art molten salt laboratory. The successful candidate will hold a senior position in our chemistry group, and will be supervising and performing experimental investigations of chemistry and materials properties in molten salts at high temperatures. Key words include laboratory planning and design, costing and scheduling, project management, procurement, safety management, supply chain management, radiation protection supervision, radioisotope tracking and inventory, quality assurance, equipment maintenance, and apparatus design. As a member of the reactor research and development team, the position will include collaboration with the reactor physics and engineering groups in Seaborg to ensure due consideration of important physical phenomena and safety considerations across all relevant disciplines. Some international travelling should be expected.

RESPONSIBILITIES

Seaborg employees must be able to act proactively and independently to perform a wide variety of functions that do not always correlate with experience or expertise (such as writing job advertisements). That being said, the advertised position is expected to include at least some of the following responsibilities and tasks:??

  • Plan, design and establish a state-of-the-art molten salt laboratory;

  • Budget costs of equipment, maintenance, running costs, consumables, etc.;

  • Procure, install and commission laboratory equipment;

  • Manage and maintain apparatus;

  • Develop, implement and enforce laboratory requirements and guidelines for quality assurance and occupational health and safety, in accordance with regional and company standards;

  • Aid the planning and execution of experimental campaigns to establish and validate chemical and materials properties in high-temperature molten salts;

  • Analyse and report findings to steer design activities;

  • Support the development of robust instrumentation and control systems for monitoring and controlling the chemistry, temperature and flow of molten salts, as well as for safeguards purposes;

  • Support IP development and acquisition activities;

  • Pursue compliance with regulatory requirements, including working to establish suitable standards and codes for the classification of salt-bearing systems, structures and components;

  • Design and develop methods to produce and purify salts;

  • Design and develop methods to perform and validate a wide range of measurements in molten salts, incl. of thermophysical properties, speciation, solubility, corrosion, heat transfer, turbulence, structural material properties, and more.

REQUIREMENTS

  • Desire to positively change the world by shaping the energy landscape of tomorrow;

  • Demonstrated ability to diligently approach and solve challenging tasks within time and budgetary constraints;

  • BSc or higher in chemistry, chemical engineering, materials science and engineering, or similar;

  • Considerable experience with setting up and/or managing a chemical laboratory;

  • Prior experience with planning, scheduling, costing and procuring scientific equipment and effectively setting up and managing appropriate supply chains;

  • Demonstrated practical skills for developing and installing scientific equipment;

  • Experience developing and/or working under effective quality assurance and operational health and safety systems in a chemical laboratory environment;

  • Experience working with molten salts, or other high-temperature and/or corrosive fluids preferred;

  • Experience from nuclear industry preferred;

  • Team player with effective communication and interpersonal skills, including fluency in English;

  • Ability to travel by plane and communicate outside of normal working hours when necessary.

 

At Seaborg we strongly value the combination of relevant experience, talent and personality traits that align with our team and overarching vision for a sustainable future. We therefore encourage applications from diverse backgrounds and are prepared to mould the job description to accommodate well-aligned candidates.

OUR OFFER

While our team is still small, our ambitions are not. Becoming a part of Seaborg presents a unique possibility to importantly impact and define the global energy landscape of tomorrow. We know that new ideas and influences are key to challenge the status quo and strive for continuous improvement, and so new hires can expect to importantly contribute to shaping both the technology and the future of the company.?

We want to play an active role in enabling the personal and professional development of all employees so that they can evolve and grow to take on changing tasks and responsibilities. To give room for this development, we practice high work flexibility in an informal, merit-based environment without strict hierarchies. With time, we expect every employee to become an invaluable part of Seaborg and our success, and we underpin this expectation by offering all new employees stock options in the company. 

We are based in Denmark, a country known for its high quality of life and extensive social welfare system. That means free health care and education, generous vacation arrangements, progressive maternity and paternity leave provisions, etc. More on this at lifeindenmark.borger.dk

Our office is situated centrally in Copenhagen - a young and vibrant European capital on the Øresund coast with a thriving expat community and world-leading bicycle infrastructure.

Seaborg ApSKøbenhavn N2019-08-20T00:00:002019-09-13T00:00:00
330075353Laborant eller bioanalytiker søges til forskning i hepatitis C virus vaccine udviklingRobot En stilling som laborant eller bioanalytiker i et år med mulighed for forlængelse er ledig til besættelse den 1. oktober 2019 eller snarest derefter. Ansættelsen er med tjeneste i Copenhagen Hepatitis C Program (CO-HEP), der er en del af Infektionsmedicinsk Afdeling på Hvidovre Hospital. CO-HEP er desuden tilknyttet Institut for Immunologi og Mikrobiologi (ISIM) på Københavns Universitet. Vores forskningsgruppe arbejder primært med cellebiologi og molekylærbiologi bag virusinfektioner. Vores fokusområde er udvikling af en vaccine mod hepatitis C virus, som inkluderer produktionen af virus i cellekultur i flasker eller bioreaktorer, oprensning af virus partikler og undersøgelse af neutraliserende antistoffer udviklet i vaccinerede mus. Forskningsgruppen CO-HEP, der ledes af Prof. Jens Bukh, har ca. 30 forskere af forskellig nationalitet tilknyttet (læger, postdocs, ph.d.-studerende, bioanalytikere, laboranter, og studerende). Du vil komme til at arbejde direkte med Lektor Judith Gottwein og hendes undergruppe på omkring syv forskere. Vi har brug for en dygtig laborant, der selvstændigt kan varetage projekter i laboratoriet i samarbejde med andre forskere. Vi forventer endvidere at du kan være med til at varetage nogle almene laboratorieopgaver. Ambitioner, samarbejde, ansvarlighed og fællesskab er nøgleord. Vi tilbyder dig således at arbejde i et dynamisk miljø, hvor fokus er rettet mod virale infektionssygdomme. De teknikker der anvendes i laboratoriet, vil primært omfatte cellearbejde som inkluderer arbejde med bioreaktorer, virus neutralisations forsøg, virus titrering, oprensning af virus, PCR, DNA kloning samt andre funktionelle forsøg. Du vil derudover få ansvarsområder i forbindelse med vedligeholdelse af laboratorier, der kan inkludere den daglige funktion af cellelaboratorium, ordrebestillinger, organisering m.v. Vi har brug for en kollega der er motiveret, ansvarsbevidst og interesseret i at samarbejde med andre for at være med til at skabe ny viden. Vi søger således en laborant eller bioanalytiker, der ønsker nye faglige udfordringer. Erfaring med cellekultur, molekylærbiologiske metoder eller bioreaktorer vil være en fordel. Meget af det daglige arbejde bliver planlagt i samarbejde med andre forskere, men der er mange selvstændige opgaver med hensyn til planlægning og udførelse, så du skal være god til at håndtere mange opgaver og planlægge din tid effektivt. Da du vil få mange internationale kollegaer, er det desuden et krav, at du har gode engelskekundskaber. Yderligere oplysning fås ved henvendelse til lektor Judith Gottwein (jgottwein@sund.ku.dk) eller Prof. Jens Bukh (jbukh@sund.ku.dk). Løn- og ansættelsesvilkår: Løn- og ansættelsesforhold sker efter gældende overenskomst med mulighed for kvalifikationstillæg. Ansøgning: Er du interesseret i stillingen, beder vi dig sende en elektronisk ansøgning med bilag via Region H´s job portal. Ansøgningen skal være bilagt CV, referencer og dokumentation for relevant uddannelse. Vi ønsker at afspejle det omgivende samfund og opfordrer alle uanset personlig baggrund til at søge stillingen. Ansøgningsfrist mandag den 16. september 2019 kl. 23.59.En stilling som laborant eller bioanalytiker i et år med mulighed for forlængelse er ledig til besættelse den 1. oktober 2019 eller snarest derefter. Ansættelsen er med tjeneste i Copenhagen Hepatitis C Program (CO-HEP), der er en del af Infektionsmedicinsk Afdeling på Hvidovre Hospital. CO-HEP er desuden tilknyttet Institut for Immunologi og Mikrobiologi (ISIM) på Københavns Universitet.

Vores forskningsgruppe arbejder primært med cellebiologi og molekylærbiologi bag virusinfektioner. Vores fokusområde er udvikling af en vaccine mod hepatitis C virus, som inkluderer produktionen af virus i cellekultur i flasker eller bioreaktorer, oprensning af virus partikler og undersøgelse af neutraliserende antistoffer udviklet i vaccinerede mus.

Forskningsgruppen CO-HEP, der ledes af Prof. Jens Bukh, har ca. 30 forskere af forskellig nationalitet tilknyttet (læger, postdocs, ph.d.-studerende, bioanalytikere, laboranter, og studerende). Du vil komme til at arbejde direkte med Lektor Judith Gottwein og hendes undergruppe på omkring syv forskere. Vi har brug for en dygtig laborant, der selvstændigt kan varetage projekter i laboratoriet i samarbejde med andre forskere. Vi forventer endvidere at du kan være med til at varetage nogle almene laboratorieopgaver. Ambitioner, samarbejde, ansvarlighed og fællesskab er nøgleord.

Vi tilbyder dig således at arbejde i et dynamisk miljø, hvor fokus er rettet mod virale infektionssygdomme. De teknikker der anvendes i laboratoriet, vil primært omfatte cellearbejde som inkluderer arbejde med bioreaktorer, virus neutralisations forsøg, virus titrering, oprensning af virus, PCR, DNA kloning samt andre funktionelle forsøg. Du vil derudover få ansvarsområder i forbindelse med vedligeholdelse af laboratorier, der kan inkludere den daglige funktion af cellelaboratorium, ordrebestillinger, organisering m.v. Vi har brug for en kollega der er motiveret, ansvarsbevidst og interesseret i at samarbejde med andre for at være med til at skabe ny viden.

Vi søger således en laborant eller bioanalytiker, der ønsker nye faglige udfordringer. Erfaring med cellekultur, molekylærbiologiske metoder eller bioreaktorer vil være en fordel. Meget af det daglige arbejde bliver planlagt i samarbejde med andre forskere, men der er mange selvstændige opgaver med hensyn til planlægning og udførelse, så du skal være god til at håndtere mange opgaver og planlægge din tid effektivt. Da du vil få mange internationale kollegaer, er det desuden et krav, at du har gode engelskekundskaber.

Yderligere oplysning fås ved henvendelse til lektor Judith Gottwein (jgottwein@sund.ku.dk) eller Prof. Jens Bukh (jbukh@sund.ku.dk).


Løn- og ansættelsesvilkår
:
Løn- og ansættelsesforhold sker efter gældende overenskomst med mulighed for kvalifikationstillæg.


Ansøgning
:
Er du interesseret i stillingen, beder vi dig sende en elektronisk ansøgning med bilag via Region H´s job portal. Ansøgningen skal være bilagt CV, referencer og dokumentation for relevant uddannelse.

Vi ønsker at afspejle det omgivende samfund og opfordrer alle uanset personlig baggrund til at søge stillingen.

Ansøgningsfrist mandag den 16. september 2019 kl. 23.59.



Hvidovre HospitalHvidovre2019-08-19T00:00:002019-09-16T00:00:00
da-DK

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