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QA Manager

Hey! We’re SYBO and we’re here to make awesome games.

Like you, we’re gamers, we’re creators, we’re perfectionists. It’s our goal to create the best experiences for everyone! Fantastic games are made by fantastic people and that’s who we’re looking for :)

 

We are searching for a full-time QA Manager to support and work embedded within one of our development teams.

Your responsibilities will include establishing and maintaining current QA processes for the game and support the team with hands-on testing. In addition, you will be the liaison between the team and external partners, scheduling functional QA, compatibility QA and localization processes.

We appreciate specialists and with your particular skill set, you will be a large part of forming the position and becoming a part of our continuous journey. Sounds interesting? Take a look at the description - and let us know if you are the one we are looking for.

 

REQUIREMENTS

QA Manager Responsibilities:

  • Perform functionality QA on the game and provide written reports on bugs, unwanted game behaviors or visual errors with clear reproduction steps.
  • Work closely with the production team to create test plans, prioritize & execute testing across all supported mobile platforms.
  • Take the lead in stakeholder management, negotiations and planning work with all external QA partners delivering services for the game.
  • Own all documentation, communication, scheduling and feedback between the team and external QA partners.
  • Collaborating and communicating with designers and stakeholders about features, requirements and acceptance criteria.
  • Drive and implement processes for automation initiatives across all aspects of testing.
  • Be a stakeholder for test tools and build server development.

You should be able to say yes to all of the following statements:

  • 3-years+ mobile testing and QA experience.
  • Have experience with Unity.
  • Great interest in F2P games, the industry and next generation technologies across multiple platforms.
  • Self-driven and taking the initiative to seeks out tasks.
  • Ability to work in both a team environment and independently.
  • Excellent written and verbal communication skills in English.
  • Strong critical and creative problem-solving abilities.
  • Strong organizational and time management skills.
  • Have a positive attitude and drive for product success.

Nice to haves:

  • Experience managing external QA services

Your application must include:

  • Brief presentation of yourself
  • Why we are the perfect match

 

BENEFITS

What we can brag about:

  • The best office location in Copenhagen
  • A chance to do the work of your life
  • An informal and creative culture where everybody is heard

We also have...

  • Health insurance for every employee
  • A pension plan
  • A healthy lunch buffet
  • Currently 17 nationalities
  • And a lot of fun - also when working


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329786025Phoenix-d567abd912018-04-03T00:00:00QA Manager

Hey! We’re SYBO and we’re here to make awesome games.

Like you, we’re gamers, we’re creators, we’re perfectionists. It’s our goal to create the best experiences for everyone! Fantastic games are made by fantastic people and that’s who we’re looking for :)

 

We are searching for a full-time QA Manager to support and work embedded within one of our development teams.

Your responsibilities will include establishing and maintaining current QA processes for the game and support the team with hands-on testing. In addition, you will be the liaison between the team and external partners, scheduling functional QA, compatibility QA and localization processes.

We appreciate specialists and with your particular skill set, you will be a large part of forming the position and becoming a part of our continuous journey. Sounds interesting? Take a look at the description - and let us know if you are the one we are looking for.

 

REQUIREMENTS

QA Manager Responsibilities:

  • Perform functionality QA on the game and provide written reports on bugs, unwanted game behaviors or visual errors with clear reproduction steps.
  • Work closely with the production team to create test plans, prioritize & execute testing across all supported mobile platforms.
  • Take the lead in stakeholder management, negotiations and planning work with all external QA partners delivering services for the game.
  • Own all documentation, communication, scheduling and feedback between the team and external QA partners.
  • Collaborating and communicating with designers and stakeholders about features, requirements and acceptance criteria.
  • Drive and implement processes for automation initiatives across all aspects of testing.
  • Be a stakeholder for test tools and build server development.

You should be able to say yes to all of the following statements:

  • 3-years+ mobile testing and QA experience.
  • Have experience with Unity.
  • Great interest in F2P games, the industry and next generation technologies across multiple platforms.
  • Self-driven and taking the initiative to seeks out tasks.
  • Ability to work in both a team environment and independently.
  • Excellent written and verbal communication skills in English.
  • Strong critical and creative problem-solving abilities.
  • Strong organizational and time management skills.
  • Have a positive attitude and drive for product success.

Nice to haves:

  • Experience managing external QA services

Your application must include:

  • Brief presentation of yourself
  • Why we are the perfect match

 

BENEFITS

What we can brag about:

  • The best office location in Copenhagen
  • A chance to do the work of your life
  • An informal and creative culture where everybody is heard

We also have...

  • Health insurance for every employee
  • A pension plan
  • A healthy lunch buffet
  • Currently 17 nationalities
  • And a lot of fun - also when working
2018-05-24T14:17:00.503 Hey! We re SYBO and we re here to make awesome games. Like you, we re gamers, we re creators, we re perfectionists. It s our goal to create the best experiences for everyone! Fantastic games are made by fantastic people and that s who we re looking for :) We are searching for a full-time QA Manager to support and work embedded within one of our development teams. Your responsibilities will include establishing and maintaining current QA processes for the game and support the team with hands-on testing. In addition, you will be the liaison between the team and external partners, scheduling functional QA, compatibility QA and localization processes. We appreciate specialists and with your particular skill set, you will be a large part of forming the position and becoming a part of our continuous journey. Sounds interesting? Take a look at the description - and let us know if you are the one we are looking for. REQUIREMENTS QA Manager Responsibilities: Perform functionality QA on the game and provide written reports on bugs, unwanted game behaviors or visual errors with clear reproduction steps. Work closely with the production team to create test plans, prioritize & execute testing across all supported mobile platforms. Take the lead in stakeholder management, negotiations and planning work with all external QA partners delivering services for the game. Own all documentation, communication, scheduling and feedback between the team and external QA partners. Collaborating and communicating with designers and stakeholders about features, requirements and acceptance criteria. Drive and implement processes for automation initiatives across all aspects of testing. Be a stakeholder for test tools and build server development. You should be able to say yes to all of the following statements: 3-years mobile testing and QA experience. Have experience with Unity. Great interest in F2P games, the industry and next generation technologies across multiple platforms. Self-driven and taking the initiative to seeks out tasks. Ability to work in both a team environment and independently. Excellent written and verbal communication skills in English. Strong critical and creative problem-solving abilities. Strong organizational and time management skills. Have a positive attitude and drive for product success. Nice to haves: Experience managing external QA services Your application must include: Brief presentation of yourself Why we are the perfect match BENEFITS What we can brag about: The best office location in Copenhagen A chance to do the work of your life An informal and creative culture where everybody is heard We also have... Health insurance for every employee A pension plan A healthy lunch buffet Currently 17 nationalities And a lot of fun - also when working11Jobnetd567abd9100000000000IDK_OFIR_02DKDanmark228DKK2018-05-28T00:00:000000https://sybo-games.workable.com/jobs/6155600EuropaDanmarkEuropaDanmarkSjælland & øerStorkøbenhavnKøbenhavn3203680SYBO ApS11Jorcks Passage 1A1161København K24642017DKDanmark0
DKDanmarkDKDanmark
8Fuldtid46Permanent547875JobNet48028921000https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=d567abd9https://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=d567abd9https://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=d567abd9&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=d567abd9&page=EmailApplyForm&component=SendApplicationButton1Dansk3Læse/ tale123906Kvalitetschef6Ledelse354139491SYBOsybo@sybogames.comDKDanmarkDKDanmark329969869QA managerRobot We are looking for a QA manager who will take a leading role in all aspects related to quality assurance of BluSense s point-of-care testing products. Do you want to work in a rapidly growing med-tech startup and make a real impact on the lives of people affected by dengue, Zika and other tropical diseases? Can you imagine yourself being a part of a dynamic, international team with colleagues from more than 17 countries? If yes, wait no longer and apply now! We are excited to hear from you! The position: You will take a leading role in all aspects related to quality assurance of BluSense s point-of-care testing products. You will work in close collaboration with management, R D and production to ensure that all quality standards are met at BluSense Denmark, where ViroTrack cartridges are developed and produced. Furthermore, you will provide support to the quality assurance team at our subsidiary BluSense Biotech in Taiwan, where hardware and software development and manufacturing is performed. Responsibilities: • Improve and maintain the Quality Management System and Quality Policy in cooperation with Top Management • Responsible for managing the overall quality at BluSense Diagnostics • Coordinate and supervise quality related activities at our subsidiary BluSense Biotech in Taiwan (occasional travelling might be required) • Ensure that all applicable quality requirements are clearly defined and implemented supporting the effective Design transfer of new updated products from R D into Manufacturing • Assure that the assigned product portfolio and applicable processes and procedures remain in compliance with IVD regulatory and ISO 13485:2016 Quality requirements • Review all current inspection and testing protocols utilized within the assigned product portfolio and develop continuous improvement initiatives to assure that all design control document templates are efficient, effective and fit the purpose and are simple to use • Assist R D in defining the quality requirements in the evaluation of new or alternatively sources for components and monitor evaluate manufacturing trial activities • Conduct internal Quality audits and coordinate external Quality audits • Collaborate cross-functionally with R D and Manufacturing to resolve product life cycle quality issues • Ensure that all quality KPIs are kept current and ensure the product process quality feedback to the organization in a clear and standardized way • Ensure that Quality Management Reviews are prepared and carried through regularly • Ensure maintenance of the QMS system and ensure regular training and development of the organization • Supporting R D during the development and documentation of novel products • Investigate and Manage all internal and external discrepancies (non-conformance, CAPAs, etc.) are adequately documented, registered and resolved in alignment with internal procedures • Occasional travelling will be required, both within Denmark and internationally Qualifications: • You are highly motivated and can work well alone but also as part of a team. • Minimum Bachelor s degree in science (biology, chemistry, medical technology or other), engineering or medical fields • At least 2 years of experience in a similar role in a regulated industry (e.g. medical devices, IVD) • Knowledge of ISO 13485:2016, directive 98 79 EC and IVDR • Fluency in English, both verbally and in writing • Ability to manage projects and adhere to timelines • Ability to work in an international environment with cross-functional teams • You like to work in a fast-paced start-up environment • International experience is a plus What we offer • A dynamic working environment • Co-operation and exchange of ideas within a multinational and interdisciplinary team • You will have a leading role in bringing to market a novel point-of-care device How to apply: We will process applications as they arrive. Therefore, please submit your application and CV as soon as possible and no later than April 1st. Qualified applicants can expect to be called for an interview before the deadline. Send us your application via the hub at https: thehub.dk jobs qa-manager-1. For questions regarding this position please contact Robert Burger, COO (robert@blusense-diagnostics.com). About BluSense Diagnostics: BluSense Diagnostics is a young and dynamic MedTech company, spin-off in 2015 from the Department of Micro- and Nanotechnology, Technical University of Denmark. The company is developing a point-of-care blood testing device for infectious diseases, based on a novel nanotechnology-based biosensing method, leveraging hardware and consumables developed from the optical storage industry.

We are looking for a  QA manager who will take a leading role in all aspects related to quality assurance of BluSense’s point-of-care testing products.

Do you want to work in a rapidly growing med-tech startup and make a real impact on the lives of people affected by dengue, Zika and other tropical diseases? Can you imagine yourself being a part of a dynamic, international team with colleagues from more than 17 countries? If yes, wait no longer and apply now! We are excited to hear from you!

The position:

You will take a leading role in all aspects related to quality assurance of BluSense’s point-of-care testing products. You will work in close collaboration with management, R&D and production to ensure that all quality standards are met at BluSense Denmark, where ViroTrack cartridges are developed and produced. Furthermore, you will provide support to the quality assurance team at our subsidiary BluSense Biotech in Taiwan, where hardware and software development and manufacturing is performed.

Responsibilities:

•    Improve and maintain the Quality Management System and Quality Policy in cooperation  with Top Management
•    Responsible for managing the overall quality at BluSense Diagnostics
•    Coordinate and supervise quality related activities at our subsidiary BluSense Biotech in Taiwan (occasional travelling might be required)
•    Ensure that all applicable quality requirements are clearly defined and implemented supporting the effective Design transfer of new/updated products from R&D into Manufacturing
•    Assure that the assigned product portfolio and applicable processes and procedures remain in compliance with IVD regulatory and ISO 13485:2016 Quality requirements
•    Review all current inspection and testing protocols utilized within the assigned product portfolio and develop continuous improvement initiatives to assure that all design control document templates are efficient, effective and fit the purpose and are simple to use
•    Assist R&D in defining the quality requirements in the evaluation of new or alternatively sources for components and monitor/evaluate manufacturing trial activities
•    Conduct internal Quality audits and coordinate external Quality audits
•    Collaborate cross-functionally with R&D and Manufacturing to resolve product life cycle quality issues
•    Ensure that all quality KPIs are kept current and ensure the product/process quality feedback to the organization in a clear and standardized way
•    Ensure that Quality Management Reviews are prepared and carried through regularly
•    Ensure maintenance of the QMS system and ensure regular training and development of the organization
•    Supporting R&D during the development and documentation of novel products
•    Investigate and Manage all internal and external discrepancies (non-conformance, CAPAs, etc.) are adequately documented, registered and resolved in alignment with internal procedures
•    Occasional travelling will be required, both within Denmark and internationally

Qualifications:

•    You are highly motivated and can work well alone but also as part of a team.
•    Minimum Bachelor’s degree in science (biology, chemistry, medical technology or other), engineering or medical fields
•    At least 2 years of experience in a similar role in a regulated industry (e.g. medical devices, IVD)
•    Knowledge of ISO 13485:2016, directive 98/79/EC and IVDR
•    Fluency in English, both verbally and in writing
•    Ability to manage projects and adhere to timelines
•    Ability to work in an international environment with cross-functional teams
•    You like to work in a fast-paced start-up environment
•    International experience is a plus

What we offer

•    A dynamic working environment
•    Co-operation and exchange of ideas within a multinational and interdisciplinary team
•    You will have a leading role in bringing to market a novel point-of-care device

How to apply:

We will process applications as they arrive. Therefore, please submit your application and CV as soon as possible and no later than April 1st. Qualified applicants can expect to be called for an interview before the deadline.

Send us your application via the hub at https://thehub.dk/jobs/qa-manager-1.

For questions regarding this position please contact Robert Burger, COO (robert@blusense-diagnostics.com).

 

About BluSense Diagnostics:

BluSense Diagnostics is a young and dynamic MedTech company, spin-off in 2015 from the Department of Micro- and Nanotechnology, Technical University of Denmark. The company is developing a point-of-care blood testing device for infectious diseases, based on a novel nanotechnology-based biosensing method, leveraging hardware and consumables developed from the optical storage industry.

 

BLUSENSE DIAGNOSTICS APSKøbenhavn Ø2019-03-04T00:00:002019-04-01T00:00:00
329981126Kvalitetschef / Inspektør (Rengøring)Robot Kvalitetschef Inspektør (Rengøring) - Område: Øst Danmark PartnerService er en dynamisk virksomhed i konstant vækst og udvikling. Vi søger en engageret kvalitetschef i Øst Danmark. Som kvalitetschef i PartnerService har du bl.a. ansvaret for kvaliteten af den daglige rengøring hos en række af vores kunder, herunder også personaleansvaret for de serviceassistenter der er tilknyttet de respektive pladser. Vi tilbyder: En spændende og alsidig arbejdsdag Egne ansvarsområder Gode kolleger Planlægning af egne opgaver og arbejdsdag En virksomhed i konstant udvikling og vækst Fri mobiltelefon (iPhone) og tablet (iPad) Profilbeklædning til arbejdsbrug Varebil på gule plader til arbejdsmæssig brug Løn efter kvalifikationer Dine kvalifikationer: Erfaring fra lignende job Har kørekort (B) Fornuftige mundtlige og skriftlige dansk- og engelske kundskaber Er en god holdspiller men tager selv initiativ og ansvar Kan arbejde selvstændigt og målrettet, og har et godt overblik Er udadvendt, servicemindet og flexibel Du har smil på læben, ben i næsen, og glimt i øjet Hvis ovenstående lyder som noget for dig, så send din ansøgning hurtigst muligtmed Kvalitetschef skrevet i emnefeltet til os på mail: mene@partnerservice.dk Vedhæft: CV Anbefalinger Tiltrædelse: Hurtigst muligt efter aftale Ved evt. personlig samtale bedes kopi af straffeattest samt kontaktoplysninger på evt. referencer medbringes. PartnerService blev etableret i 2003, og har hovedkontor i København. Vi servicerer 500 kunder fordelt over det meste af landet, og vi beskæftiger 450 stærkt motiverede medarbejdere. Vi er en servicevirksomhed indenfor kontor- og specialrengøring, salg af forbrugsvarer, måtte- og planteservice, viceværtopgaver, vinduespolering samt øvrige facility opgaver.

Kvalitetschef / Inspektør (Rengøring) - Område: Øst Danmark

PartnerService er en dynamisk virksomhed i konstant vækst og udvikling.

Vi søger en engageret kvalitetschef i Øst Danmark. Som kvalitetschef i PartnerService har du bl.a. ansvaret for kvaliteten af den daglige rengøring hos en række af vores kunder, herunder også personaleansvaret for de serviceassistenter der er tilknyttet de respektive pladser.

Vi tilbyder:

  • En spændende og alsidig arbejdsdag
  • Egne ansvarsområder
  • Gode kolleger
  • Planlægning af egne opgaver og arbejdsdag
  • En virksomhed i konstant udvikling og vækst
  • Fri mobiltelefon (iPhone) og tablet (iPad)
  • Profilbeklædning til arbejdsbrug
  • Varebil på gule plader til arbejdsmæssig brug
  • Løn efter kvalifikationer

Dine kvalifikationer:

  • Erfaring fra lignende job
  • Har kørekort (B)
  • Fornuftige mundtlige og skriftlige dansk- og engelske kundskaber
  • Er en god holdspiller – men tager selv initiativ og ansvar
  • Kan arbejde selvstændigt og målrettet, og har et godt overblik
  • Er udadvendt, servicemindet og flexibel
  • Du har smil på læben, ben i næsen, og glimt i øjet

Hvis ovenstående lyder som noget for dig, så send din ansøgning hurtigst muligtmed ’Kvalitetschef’ skrevet i emnefeltet til os på mail:

  • mene@partnerservice.dk

Vedhæft:

  • CV
  • Anbefalinger

Tiltrædelse:

  • Hurtigst muligt / efter aftale

Ved evt. personlig samtale bedes kopi af straffeattest samt kontaktoplysninger på evt. referencer medbringes.

PartnerService blev etableret i 2003, og har hovedkontor i København. Vi servicerer 500 kunder fordelt over det meste af landet, og vi beskæftiger 450 stærkt motiverede medarbejdere. Vi er en servicevirksomhed indenfor kontor- og specialrengøring, salg af forbrugsvarer, måtte- og planteservice, viceværtopgaver, vinduespolering samt øvrige facility opgaver.

PARTNERSERVICE HVER GANG ApSKøbenhavn SV2019-03-20T00:00:002019-03-24T00:00:00
329981067Operations ManagerRobot Are you looking for a chance to work in an international setting where you can influence and initiate actions to improve existing conditions and processes? Do you thrive in a dynamic setting where you are dealing with changes on a daily basis? And do you have an open mind to new ideas, at the same time ensuring relevance and meaningfulness in all new endeavors then we might have the right job for you. About the department Local Manufacturing (LM) is part of Novo Nordisk s Product Supply organization responsible for Novo Nordisk Local Manufacturing sites and Local Manufacturing Contract Manufacturing Operations (CMO) s. Our main office is located in Bagsværd, Denmark. LM is responsible for Novo Nordisk sites and CMOs in markets where local manufacturing is considered a requirement. Our sites and CMOs are located in Russia, Algeria, Iran, Egypt, India and Bangladesh, more countries may be added in future as local manufacturing projects become operational. The area is dynamic and fast paced with a strong focus on local requirements and driving change. The position As Operations Manager in LM, you will be responsible for centrally supporting the daily operation of selected CMOs and Novo Nordisk local sites (and can act as back-up for other Operations Managers), mainly within Aseptic Production, ensuring our products are delivered by the local sites or the CMOs to Novo Nordisk affiliates timely and at the right level of quality. You will coordinate with sales affiliates and with Product Supply organization to balance capacity and demand. The role includes timely follow up on delivery performance, quality performance and ensuring products are delivered to our internal customers. Furthermore, the role involves working with stakeholders across Novo Nordisk to problem solve and improve the performance at the CMOs. You will be the part of a team responsible for central coordination on supply chain in Novo Nordisk with Local Manufacturing. Working location will be in Bagsværd and travelling is an integrated part of your job to some extent, around 15-30 days per year. The position is temporary for 24 months. Qualifications You hold a Master s degree within e.g. Supply Chain, Pharmacy, Engineering or similar. Your theoretical background should be combined with good practical experience within the pharmaceutical business, manufacturing and supply chain management. Experience with manufacturing of Aseptic production techniques is an advantage. You should be able to use your strong technical and business understanding too. You will be part of several teams both formally and informally hence the ability to work across boundaries is critical for your success. We expect you to make procedural or process suggestions and decisions for achieving team goals and promote drive simplicity in both Novo Nordisk and CMOs processes or performing team functions providing necessary resources and help to remove obstacles ensuring that the team accomplishing goals. As a person you are good at building trust with stakeholders and you naturally share important and relevant information with your team. You have an analytical mind-set with the ability to work in a structured way and an ability to support multiple activities. The position requires high degree of independent decision making (managerial and professional) on behalf of Novo Nordisk and Local Manufacturing in an international context under sometimes challenging conditions due to cultural, national or political restrictions when operating globally in e.g. Algeria, Egypt and Saudi Arabia. The position has direct impact on the sales of products in the local markets. In addition, the position requires good understanding of the relevant Novo Nordisk and EU GMP standards to confirm the CMO s adherence to these standards and be able to combine technical and business acumen to drive the Novo Nordisk business in local markets. Preferably you have experience from an international environment. Furthermore, you have strong communication skills in the English language. Working at Novo Nordisk At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference. Contact For further information, please call Christophe Moyer on 45 3077 7158 Deadline Please upload your application and CV no later than the 31st March 2019. Interviews will take place ongoing. Millions rely on us To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

Are you looking for a chance to work in an international setting where you can influence and initiate actions to improve existing conditions and processes? Do you thrive in a dynamic setting where you are dealing with changes on a daily basis? And do you have an open mind to new ideas, at the same time ensuring relevance and meaningfulness in all new endeavors then we might have the right job for you.
 
About the department
Local Manufacturing (LM) is part of Novo Nordisk’s Product Supply organization responsible for Novo Nordisk Local Manufacturing sites and Local Manufacturing Contract Manufacturing Operations (CMO)’s. Our main office is located in Bagsværd, Denmark. LM is responsible for Novo Nordisk sites and CMOs in markets where local manufacturing is considered a requirement. 

Our sites and CMOs are located in Russia, Algeria, Iran, Egypt, India and Bangladesh, more countries may be added in future as local manufacturing projects become operational. The area is dynamic and fast paced with a strong focus on local requirements and driving change.

The position
As Operations Manager in LM, you will be responsible for centrally supporting the daily operation of selected CMOs and Novo Nordisk local sites (and can act as back-up for other Operations Managers), mainly within Aseptic Production, ensuring our products are delivered by the local sites or the CMOs to Novo Nordisk affiliates timely and at the right level of quality. You will coordinate with sales affiliates and with Product Supply organization to balance capacity and demand. 

The role includes timely follow up on delivery performance, quality performance and ensuring products are delivered to our internal customers. Furthermore, the role involves working with stakeholders across Novo Nordisk to problem solve and improve the performance at the CMOs. You will be the part of a team responsible for central coordination on supply chain in Novo Nordisk with Local Manufacturing.

Working location will be in Bagsværd and travelling is an integrated part of your job to some extent, around 15-30 days per year. The position is temporary for 24 months.


Qualifications
You hold a Master’s degree within e.g. Supply Chain, Pharmacy, Engineering or similar. Your theoretical background should be combined with good practical experience within the pharmaceutical business, manufacturing and supply chain management. Experience with manufacturing of Aseptic production techniques is an advantage. You should be able to use your strong technical and business understanding too.
 
You will be part of several teams both formally and informally hence the ability to work across boundaries is critical for your success. We expect you to make procedural or process suggestions and decisions for achieving team goals and promote/drive simplicity in both Novo Nordisk and CMOs processes or performing team functions; providing necessary resources and help to remove obstacles ensuring that the team accomplishing goals. 

As a person you are good at building trust with stakeholders and you naturally share important and relevant information with your team. You have an analytical mind-set with the ability to work in a structured way and an ability to support multiple activities.
 

The position requires high degree of independent decision making (managerial and professional) on behalf of Novo Nordisk and Local Manufacturing in an international context under sometimes challenging conditions due to cultural, national or political restrictions when operating globally in e.g. Algeria, Egypt and Saudi Arabia. 

The position has direct impact on the sales of products in the local markets. In addition, the position requires good understanding of the relevant Novo Nordisk and EU GMP standards to confirm the CMO’s adherence to these standards and be able to combine technical and business acumen to drive the Novo Nordisk business in local markets.  

Preferably you have experience from an international environment. Furthermore, you have strong communication skills in the English language. 


Working at Novo Nordisk
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
 
Contact
For further information, please call Christophe Moyer on +45 3077 7158

Deadline

Please upload your application and CV no later than the 31st March 2019. Interviews will take place ongoing. 

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

NOVO NORDISK A/SBagsværd2019-03-19T00:00:002019-03-31T00:00:00
da-DK

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