Lediga jobb som Kemister i Ängelholm

Är du intresserad av att arbeta med laboratorie-och kvalitetsarbete? Är du strukturerad och ansvarstagande, då kan detta vara tjänsten för dig! Om tjänsten: Som Labbassistent är du delaktig i det dagliga laboratorie- och kvalitetsarbetet. Arbetet sker i nära kontakt med två kollegor på kvalitetsavdelningen. Tjänsten är ett vikariat på 3månader, med chans till förlägning. Huvudsakliga arbetsuppgifter för tjänsten:
Re-validera analysmetoder för HPLC/UPLC
Utföra och dokumentera validering
Utföra analyser enligt uppsatta krav
Vara behjälplig på flera arbetsmoment inom området.

Vem är du? Som person är du noggrann, strukturerad, målorienterad och strävar efter att skapa förbättringar. Andra viktiga egenskaper är du är ansvarstagande och har ett stort öga för detaljer. Krav för tjänsten: Relevant arbetslivserfarenhet från laborativt arbete Erfarenhet inom HPLC / UPLC Körkort och tillgång till bil (kollektivtrafik är ej möjlig)

Meriterande: Erfarenhet inom Waters & Empower Validering av analysmetoder Högskoleutbildning inom relevant område För resor till och från arbetsplatsen krävs körkort och tillgång till bil. Omfattning: Heltid, långsiktigt behov, arbetet sker dagtid.

Ansökan
Varmt välkommen med din ansökan via ansökningslänk nedan! Ansökningarna behandlas löpande och konfidentiellt. Observera att vi ej har möjlighet att behandla ansökningar som inkommer via mail eller andra kanaler. Vid frågor om tjänsten når du oss under vardagar, kl. 08-17 på 042-21 02 99. Läs gärna mer om oss på www.processbemanning.se. Visa mindre

Är du intresserad av att arbeta med laboratorie-och kvalitetsarbete? Är du strukturerad och ansvarstagande, då kan detta vara tjänsten för dig! Om tjänsten: Som Labbassistent är du delaktig i det dagliga laboratorie- och kvalitetsarbetet. Arbetet sker i nära kontakt med två kollegor på kvalitetsavdelningen. Tjänsten är ett vikariat på 3månader, med chans till förlägning. Huvudsakliga arbetsuppgifter för tjänsten:
Re-validera analysmetoder för HPLC/UPLC
Utföra och dokumentera validering
Utföra analyser enligt uppsatta krav
Vara behjälplig på flera arbetsmoment inom området.

Vem är du? Som person är du noggrann, strukturerad, målorienterad och strävar efter att skapa förbättringar. Andra viktiga egenskaper är du är ansvarstagande och har ett stort öga för detaljer. Krav för tjänsten: Relevant arbetslivserfarenhet från laborativt arbete Erfarenhet inom HPLC / UPLC Körkort och tillgång till bil (kollektivtrafik är ej möjlig)

Meriterande: Erfarenhet inom Waters & Empower Validering av analysmetoder Högskoleutbildning inom relevant område För resor till och från arbetsplatsen krävs körkort och tillgång till bil. Omfattning: Heltid, långsiktigt behov, arbetet sker dagtid.

Ansökan
Varmt välkommen med din ansökan via ansökningslänk nedan! Ansökningarna behandlas löpande och konfidentiellt. Observera att vi ej har möjlighet att behandla ansökningar som inkommer via mail eller andra kanaler. Vid frågor om tjänsten når du oss under vardagar, kl. 08-17 på 042-21 02 99. Läs gärna mer om oss på www.processbemanning.se. Visa mindre

Är du intresserad av att arbeta med laboratorie-och kvalitetsarbete? Är du strukturerad och ansvarstagande, då kan detta vara tjänsten för dig! Om tjänsten: Som Labbassistent är du delaktig i det dagliga laboratorie- och kvalitetsarbetet. Arbetet sker i nära kontakt med två kollegor på kvalitetsavdelningen. Tjänsten är ett vikariat på 3månader, med chans till förlägning. Huvudsakliga arbetsuppgifter för tjänsten:
Re-validera analysmetoder för HPLC/UPLC
Utföra och dokumentera validering
Utföra analyser enligt uppsatta krav
Vara behjälplig på flera arbetsmoment inom området.

Vem är du? Som person är du noggrann, strukturerad, målorienterad och strävar efter att skapa förbättringar. Andra viktiga egenskaper är du är ansvarstagande och har ett stort öga för detaljer. Krav för tjänsten: Relevant arbetslivserfarenhet från laborativt arbete Erfarenhet inom HPLC / UPLC Körkort och tillgång till bil (kollektivtrafik är ej möjlig)

Meriterande: Erfarenhet inom Waters & Empower Validering av analysmetoder Högskoleutbildning inom relevant område För resor till och från arbetsplatsen krävs körkort och tillgång till bil. Omfattning: Heltid, långsiktigt behov, arbetet sker dagtid.

Ansökan
Varmt välkommen med din ansökan via ansökningslänk nedan! Ansökningarna behandlas löpande och konfidentiellt. Observera att vi ej har möjlighet att behandla ansökningar som inkommer via mail eller andra kanaler. Vid frågor om tjänsten når du oss under vardagar, kl. 08-17 på 042-21 02 99. Läs gärna mer om oss på www.processbemanning.se. Visa mindre

Do you want to make a difference by developing key lifesaving medical device products? In a truly global business who refuse to compromise when it comes to caring for people.
You will be part of a QA team that today consists of fourteen people with different background and experience. The team is responsible for quality assurance and quality development activities within the core processes Supply Chain Management and Product Lifecycle Management. This includes QA expertise during product development, production and further development of the already released products and manufacturing processes, handling of non-conformities as well as the qualification, auditing and monitoring of suppliers.
As a QA Supplier Specialist you will work in a cross functional team mainly with Purchasing, and with regular contacts with Production, R&D and Marketing and provide QA expertise and guidance to ensure safe, reliable and compliant components from qualified suppliers. You will manage the documentation of the supplier qualification process as well as re-qualifications. In this position you will also plan and perform supplier audits according to internal requirements.
We offer you an exciting possibility to join our fantastic team creating tomorrow’s solutions for Point of Care testing making peoples life’s better.
Responsibilities
Ensure that activities, within supplier management are in compliance with applicable requirements such as ISO 13485, QSR and MDSAP as well as industry standard
Maintain and ensure compliance to the supplier management procedures and internal requirements (qualifications, re-qualifications, monitoring and audits)
Active participation in weekly Procurement Review Boards
Present the supplier management process including supplier records at internal and external audits

Qualifications
To qualify for the position, you need University degree in science or technology or documented experience from a similar position.
We also believe that a candidate has the following profile:
Minimum five years of experience from a QA position from the Medical Device Industry or similar including experience in performing audits
Strong communication skills and can motivate and inspire your colleagues, even when there are conflicting demands
Ability to understand medical device regulations and standards. It is an advantage if you have knowledge and are trained in relevant standards and regulations, QSR, ISO 13485, ISO 14971, MDSAP
Fluent in English and Swedish in writing and speaking

Personality
To succeed as a QA Supplier Specialist you need to be systematic and organized, you also need to value and enjoy good teamwork. Furthermore, we believe that a can-do attitude and ability to prioritize in a fast paced environment is key. You also enjoy working in a company that aims to continuously improve, both in terms of equipment and processes.
Interviews will be held as soon as relevant candidates have been identified
Send your application via www.hemocue.com/careers. We are not able to receive your application by other means than through “careers“. Any application by mail or e-mail will be returned.
We offer you
A unique opportunity to work in the field of medical technologies, where knowledge sharing and professional respect combined makes it both fun and meaningful to go to work. You will meet enthusiastic colleagues in both Sweden and abroad who take pride in making a difference in a company whose products can truly impact other people's lives. We offer you 'freedom with responsibility', opportunities for training and career development.
The position is a full-time position with flexible location. We can offer you an office space in either our head office in Ängelholm or in our brand-new satellite office in Lund.
We are looking forward to receiving your application no later than December 12, 2021.
For further information, please contact Manager QA Operations, Björn Bylander +46 431 48 12 87.
Union contacts: Henrik Pommer, Unionen +46 431 48 12 44 or Elin Söderlind, Akademikerföreningen, +46 431 48 12 62.
When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
If you’ve ever wondered what’s within you, there’s no better time to find out. Visa mindre

HemoCue, a Danaher company since April 2013, is a global leader in Hb point-of-care testing. In 1982, HemoCue AB (Ängelholm, Sweden), introduced the first accurate, near-patient hemoglobin test. We offer point-of-care tests for hemoglobin, glucose, urine albumin, HbA1c, total and differential white blood cell count. Further information available at www.hemocue.com
Do you want to make a difference by developing and ensuring access to key lifesaving medical device products? All this in a global business who refuse to compromise when it comes to caring for people.
It is vitally important for the company to stay on top of the ever-evolving regulatory landscape around the world and understand the impact it might have on the HemoCue business and product portfolio. We are now looking for the right candidate that in the future will play an important role for the regulatory strategies to come for HemoCue.
You will be part of a RA team that today consists of eight people with different backgrounds, knowledge, and experience. As a RA Expert, you will be working in cross functional teams together with the other major functions withing the organisation e.g. R&D, Operations, Sales and Marketing, where you will be providing RA expertise and guidance to ensure safe, reliable and compliant products.
We offer you an exciting possibility to join our fantastic team creating tomorrows solutions for Point of Care testing making peoples life’s better.
Responsibilities
Monitoring, interpretation and communication of regulatory requirements
Support the organization in regulatory strategies for new product developments
Compilation and maintenance of regulatory submissions
Lead and coordinate regulatory Q&A sessions with regulatory authorities

Qualifications
Proven good knowledge of regulations for IVD products (EU IVDD/IVDR, US FDA regulations 21 CFR), standards/regulations for quality management systems (ISO 13485, QSR) and risk management for medical devices (ISO 14971)
Experience of similar products and/or other medical devices
Profound experience as MS Office user
Fluent in English and Swedish verbally and in writing

Personality
To succeed as a RA Expert you need to be systematic and flexible you also need to value and enjoy good teamwork. Furthermore we believe that a can do attitude and ability to prioritize in a fast paced environment is key. You also enjoy working in a company that aims to continuously improve, both in terms of equipment and processes.
Interviews will be held as soon as relevant candidates have been identified
Send your application via www.hemocue.com/careers. We are not able to receive your application by other means than through “careers site“.
We offer you
A unique opportunity to work in the field of medical technologies, where knowledge sharing and professional respect combine to make it both fun and meaningful to go to work. Both in Sweden and abroad you will meet enthusiastic colleagues who take pride in making a difference in a company whose products can truly impact other people's lives. We offer you 'freedom with responsibility', opportunities for training and career development.
The position is a full-time position with flexible location we can offer you an office space in either our head office in Ängelholm or in our brand-new satellite office in Lund.
We are looking forward to receiving your application no later than September 15.
For further information, please contact Director Regulatory Affairs, Rikard Almåker at tel. +46 734 14 03 89.
Union contacts: Björn Bylander, Unionen, +46 431 48 12 87 or Elin Söderlind, Akademikerföreningen, +46 431 48 12 62.
About Danaher
Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries. A globally diverse team of 71,000 associates, we are united by our culture and operating system, the Danaher Business System, which is our competitive advantage. In 2014, we generated $19.9B in revenue and our market cap exceeded $60B. We are #149 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 2,000% over 20yrs.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team. Visa mindre

HemoCue, a Danaher company since April 2013, is a global leader in Hb point-of-care testing. In 1982, HemoCue AB (Ängelholm, Sweden), introduced the first accurate, near-patient hemoglobin test. We offer point-of-care tests for hemoglobin, glucose, urine albumin, HbA1c, total and differential white blood cell count. Further information available at www.hemocue.com
Do you want to make a difference by developing key lifesaving medical device products? In a truly global business who refuse to compromise when it comes to caring for people.
You will be part of a QA team that today consists of nine people with different background and experience. The team is responsible for quality assurance and quality development activities within the core processes Supply Chain Management and Product Lifecycle Management. This includes QA expertise during product development, production and further development of the already released products and manufacturing processes, handling of non-conformities as well as the qualification, auditing and monitoring of suppliers.
As a QA Design Specialist, you will be working in a cross functional team with R&D, Operations and Marketing and provide QA expertise and guidance to ensure safe, reliable and compliant products during new product development and maintenance of existing products.
We offer you an exciting possibility to join our fantastic team creating tomorrows solutions for Point of Care testing making peoples life’s better.
Responsibilities
Core Team Member Quality in Development Project performing activities according to HemoCue’s Product Life Cycle Management process
Risk Coordinator in regard to review of risk analyses, plans and overall residual risk reports
Support the organization with Design Control expertise
Coordinate Quality Assurance activities related to Engineering Change Order process

Qualifications
To qualify for the position, you need experience from QA or R&D in Medical Device industry or a QA role with focus on supporting R&D with QA expertise in a regulated industry. In addition to this you need:
University degree in science or technology
Knowledge and trained in relevant standards and regulations (ISO 13485, ISO 14971)
Fluent in English in writing and speaking, Swedish skills is a plus

Experience within Usability Engineering, FDA Quality System Requirements, Software Validation and Cybersecurity and Project Management is a merit.
Personality
To succeed as a QA Design Specialist you need to be systematic and analytical you also need to value and enjoy good teamwork. Furthermore we believe that a can do attitude and ability to prioritize in a fast paced environment is key. You also enjoy working in a company that aims to continuously improve, both in terms of equipment and processes.
Interviews will be held as soon as relevant candidates have been identified
Send your application via www.hemocue.com/careers. We are not able to receive your application by other means than through “careers“. Any application by mail or e-mail will be returned.
We offer you
A unique opportunity to work in the field of medical technologies, where knowledge sharing and professional respect combined makes it both fun and meaningful to go to work. You will meet enthusiastic colleagues in both Sweden and abroad who take pride in making a difference in a company whose products can truly impact other people's lives. We offer you 'freedom with responsibility', opportunities for training and career development.
The position is a full-time position with flexible location we can offer you an office space in either our head office in Ängelholm or in our brand-new satellite office in Lund.
We are looking forward to receiving your application no later than September 15, 2021.
For further information, please contact Director Quality Assurance, Ola Lindau [email protected]
Union contacts: Björn Bylander, Unionen +46 431 48 12 87 or Elin Söderlind, Akademikerföreningen, +46 431 48 12 62.
About Danaher
Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries. Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team. Visa mindre

AB Cernelle är ett svenskt läkemedelsföretag med forskning, utveckling, tillverkning och distribution av läkemedel inom urologin, med särskilt fokus på kronisk prostatit (CP/CPPS) och godartad prostataförstoring (BPH). Företaget har utvecklat växtbaserade läkemedel av högkvalitativa pollenextrakt sedan 1953. Med över 50 miljoner dygnsdoser per år är Cernitol® ett av världens mest använda läkemedel vid godartade prostatabesvär. Bolaget omsätter 70 Mkr med god lönsamhet och har drygt 35 anställda på anläggningen utanför Ängelholm. www.cernelle.com


Analytisk kemist
Vill du vara med och förstärka vår organisation inom QC & Development som analytisk kemist? Har du erfarenhet av laboratoriearbete och kvalitet och är serviceinriktad, strukturerad och noggrann?
 
Vi erbjuder arbete i ett nybyggt laboratorium med ett varierat utbud av analyser inom både kemi och mikrobiologi. Vi är en serviceorganisation till vår produktion och i takt med att företaget expanderar behöver vi modernisera analysmetoder och effektivisera arbetssätt för att kunna möta behovet av fler och högkvalitativa analyser. Detta arbete vill vi gärna ha dig med i.


Arbetsuppgifter
Som analytisk kemist kommer du att arbeta med
 
·       Provtagning och analys av råvaror enligt farmakopémetoder
·       Våtkemisk och kromatografisk analys av intermediat och färdig produkt
·       Kontroller, underhåll, inköp och kvalificering av analysinstrument och annan utrustning
·       Uppdatering och författande av instruktioner och analysmetoder
·       Utredning av analysresultat i samband med avvikelser från specifikation
·       Planering, utförande och avrapportering av stabilitetsstudier
·       Modifiering och validering av analysmetoder i samarbete med vår utvecklare
 
Din profil
Du har högskole- eller universitetsutbildning inom analytisk kemi eller motsvarande kompetens och gedigen erfarenhet av laboratoriearbete i miljö reglerad enligt GMP eller ISO 17025. Du har arbetat med vätskekromatografi inom livsmedels- eller läkemedelsindustrin. Erfarenhet av mjukvaran Chromeleon är meriterande.
 
Du gillar laboratoriearbete och kan kombinera noggrannhet och struktur med högt tempo och flexibilitet i den dagliga planeringen. Du är tekniskt lagd och drar dig inte för att felsöka analysutrustning innan du tillkallar extern service. Du trivs i ett team där man hjälps åt med både de roliga och de mindre roliga arbetsuppgifterna. Du behärskar svenska och engelska i tal och skrift. Du är inte pollenallergisk.
  
Tjänsten är en tillsvidareanställning på heltid med placering på anläggningen utanför Ängelholm och arbetstiden är dagtid. Du rapporterar till Head of QC & Development.
 
Ansökan
Vid frågor kontakta Lena Cedergren på 0706-920211. Välkommen med din ansökan som vi vill ha senast 2020-03-08. Visa mindre

HemoCue, part of the Radiometer Group since April 2013, is a global leader in point-of-care testing. HemoCue AB (Ängelholm, Sweden), introduced in 1982 the first accurate, near-patient hemoglobin test. The company also sells point-of-care tests for glucose, urine albumin, HbA1c, total and differential white blood cell count. Further information, visit www.hemocue.com.

HemoCue develops, produces and markets medical diagnostic products that are fast and easy to use. We are now looking for a Risk Management Specialist who will be working in a global environment with exciting and innovative products.

Do you want to make a difference by developing key lifesaving medical device products? Are you an upbeat and organized person who looks for new challenges? Do you want to work for a truly global business who refuse to compromise when it comes to caring for people? If your answer is yes, you may be the candidate we are looking for!

This is a position where you will develop the risk management process and utilize it in practice to provide direction to many different processes. You will focus on continuous cross functional collaboration between different functions within the company and with other Risk Specialists within Radiometer group. You will collaborate with clinical expertise on establishment of appropriate Patient Risk Assessment for issues potentially impacting users and patient outcomes, help applying the knowledge in use and development of products and production processes.

You will have the overall responsibility and work from start to finish with the whole implementation of risk management. The work will be to lead risk management related activities for existing and new devices. You will ensure that applicable personnel are trained and have needed knowledge in relevant Regulations and tools such as FMEA and FTA.

The position will also be a coordinating role where you will assign and prioritize tasks within the QA Design and risk team to ensure that set goals are fulfilled.

You will be part of the QA team and report to Director Quality Assurance.

  The Job

To be successful, you will collaborate cross-functionally and provide your expertise by supporting, guiding, training and communicating towards the best result with your partners. Your main responsibilities and      tasks will include
Develop and maintain the risk management process
Train the organization and establish a support team of risk leaders to ensure the best support to projects and engineering change orders
Facilitate and support the organization in risk assessments
Ensure that procedures and activities related to risk management are in compliance with requirements in ISO 13485 and QSR as well as with industry standard methodology
Qualifications

You have a University degree in science or technology (Master or Bachelor)
Experience from the following areas is required
Minimum three years of experience in Risk Management from medical device industry or similar
Knowledge and trained in significant standards and regulations, QSR, ISO 13485, ISO 14971
Knowledge in Design Control is an advantage
You have strong interpersonal skills and can motivate and encourage your colleagues, even when there are conflicting demands
Good knowledge in English in speech and writing are needed.
Personality

As a person you are a teammate, efficient and structured and who loves a fast pace. You find it easy to communicate with other people and enjoy working in an environment that is motivated by continuous improvement, both in terms of equipment and processes.

Interviews will be held as soon as relevant candidates have been identified

Send your application via www.hemoce.com/jobbsidan. We are not able to receive your application by other means than through “jobbsidan“. Please bring diplomas for face-to-face interviews. Any application by mail or e-mail will be returned.

We offer you

An outstanding opportunity to work in the field of medical technologies, where knowledge sharing and professional respect combine to make it both fun and important to go to work. Both in Sweden and abroad you will meet hardworking colleagues who take pride in making a difference in a company whose products can truly have an effect on other people's lives. We offer you 'freedom with responsibility', opportunities for training and career development.

We are looking forward to receiving your application no later than August 30.

For further information, please contact Director Quality Assurance, Anna Stegmark at tel. +46 431 48 15 50.

Union contacts: Mikael Godolakis, Unionen, +46 431 48 14 66 or Elin Söderlind, Akademikerföreningen, +46 431 48 12 62.

About Danaher

Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries. A globally diverse team of 71,000 associates, we are united by our culture and operating system, the Danaher Business System, which is our competitive advantage. In 2014, we generated $19.9B in revenue and our market cap exceeded $60B. We are #149 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 2,000% over 20yrs.

At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team. Visa mindre

HemoCue, part of the Radiometer Group since April 2013, is a global leader in point-of-care testing. HemoCue AB (Ängelholm, Sweden), introduced in 1982 the first accurate, near-patient hemoglobin test. The company also sells point-of-care tests for glucose, urine albumin, HbA1c, total and differential white blood cell count. Further information, visit www.hemocue.com.

Do you want to make a difference by developing key lifesaving medical device products? Are you an energetic and organized person who looks for new challenges? Do you want to work for a truly global business who refuse to compromise when it comes to caring for people? If your answer is yes, you may be the candidate we are looking for!

As a QA System Specialist, you will work cross functionally within the HemoCue organization and support the organization with your expertise.

 

The Job

To be successful, you must collaborate cross-functionally and provide your expertise by supporting, guiding, training and communicating towards the best result with your partners. Your responsibilities and tasks will include.

Process owner for the Document Control process and thereby responsible for ensuring that the process is in compliance with applicable standards and regulations
Responsible for the document lifecycle – meaning that documents are updated, approved, released and maintained according to procedures
Process owner of the Business Management System NCR process
Designate user for SmartSolve for RA/QA within the Document Control Management process
Coordinate and host yearly GMP training and training for new employees
Coordinate Management Review
Coordinate internal and external audits
Qualifications

You have a University degree in science or technology (Master or Bachelor) or minimum 5 years’ experience of working with quality assurance in Medical Device Industry.

Experience from the following areas is required:

Good knowledge in ISO 13485 and QS Regulations
You have at least 3 years of experience form Medical Device Industry and preferably from working with document control
You are structured and have strong communication skills and can motivate and inspire your colleagues
Ability to understand Medical Device Regulations and Standards
Good knowledge of both Swedish and English in speech and writing are important.
Personality

As a person you are a teammate, efficient, structured and solution-oriented and who likes a fast pace. You find it easy to communicate with other people and enjoy working in a company that is motivated by continuous improvement, both in terms of equipment and processes.

Interviews will be held as soon as relevant candidates have been identified

Send your application via www.hemocue.com/jobbsidan. We are not able to receive your application by other means than through “jobbsidan“. Please bring diplomas for face-to-face interviews. Any application by mail or e-mail will be returned.

We offer you

A unique opportunity to work in the field of medical technologies, where knowledge sharing and professional respect combine to make it both fun and important to go to work. Both in Sweden and abroad you will meet enthusiastic colleagues who take pride in making a difference in a company whose products can truly change other people's lives. We offer you 'freedom with responsibility', opportunities for training and career development.

We are looking forward to receiving your application no later than August 28 .

For further information, please contact Director Quality Assurance, Anna Stegmark at tel. +46 431 48 15 50.

Union contacts: Mikael Godolakis, Unionen, +46 431 48 14 66 or Elin Söderlind, Akademikerföreningen, +46 431 48 12 62.

 

About Danaher

Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries. A globally diverse team of 71,000 associates, we are united by our culture and operating system, the Danaher Business System, which is our competitive advantage. In 2014, we generated $19.9B in revenue and our market cap exceeded $60B. We are #149 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 2,000% over 20yrs.

At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team. Visa mindre