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Production Manager

We are looking for a Production Manager who can lead the planning, setting up and validation of our high-throughput production line. The job will focus on scaling-up the current manufacturing capacity through the installation of a brand-new manufacturing line able to cope with high volume throughput. The candidate will be responsible of managing the budget, interfacing with suppliers, planning and hiring a dedicated team, and managing the whole production plant operations. A strong focus will be dedicated to quality control and process validation activities.

We are looking for an experienced leader in manufacturing operations with a process engineering background that will have a drive to leverage their technical background in a strategic role. The Production Manager will be part of the Danish management team. The ideal candidate has high knowledge about high-throughput manufacturing lines, quality controls, processes validation, microfluidics assembly, biochemistry and reagents quality control, medical device compliance (such as ISO13485), automation, and ideally in injection molding processes.

We are offering an international job within a highly dynamic and fast-growing medTech company with operations in Denmark and Taiwan.

Job description:

  • Responsible for setting up the high-throughput production line of microfluidics consumables in Denmark
  • Responsible for managing suppliers and keep timeline of deliverable of equipment and assembly of the production line
  • Responsible for managing the production department budget in close connection with the CEO
  • Hiring, training, and developing of a highly motivated workforce to elevate the skill level of employees as well as provide flexibility in a multi-functional workforce environment
  • Responsible for managing and maintaining all safety and environmental standards and operating the areas of responsibility within quality, delivery, cost and profit objectives. Lead and manage all resources to ensure the achievement of all KPI’s.
  • Responsible to maximize manufacturing efficiencies consistent with approved quality specifications by developing programs for continuous improvement utilizing the root cause analysis process.
  • Responsible for optimization to reduce cost and to ensure that production flow is up to date
  • Supports quality control programs that are designed to ensure product safety and quality that are consistent with established operating practices.
  • Responsible for defining clear goals and roles to achieve higher performance and output in medium-scale and large-scale production lines.
  • Schedule maintenance requests, equipment shutdowns, and major repairs to maintain production and quality levels.
  • Conduct audits and support the value stream’s position during customer and other audits.
  • Responsible for development of automation processes and quality control processes
  • Responsible for updated production documentation maintenance

 

Qualifications

  • We expect ambitious candidates who have excellent track record of achievements and broad experience in dealing with medical device production processes
  • Proven ability to lead people. Familiarization with the product line and the production processes.
  • Knowledge of budgets, cost analysis, variance analysis, manpower planning, training, project management.
  • Minimum of 3 years of relevant work experience within leadership of manufacturing lines in medical devices and/or other regulated environments (e.g. pharma)
  • Ideally familiar with lean and 5S methodology for production flow
  • English on negotiation level. Knowledge of Mandarin is a plus.

Personal skills

  • Excellent analytical skills and problem-solving capabilities to determine risk assessment
  • Strong drive and willingness to walk the extra mile
  • High degree of dynamic and showing the direction
  • High degree of comfort in working with Asian partners

We offer

  • A challenging and fast-growing working environment with strong Danish-Taiwanese cooperation
  • Co-operation and exchange of ideas within a multinational management/employees company
  • Professional and personal development in scaling a high-tech international company
  • Competitive compensation and benefits

 

How to apply

Please feel free to send a CV and a cover letter to careers@blusense-diagnostics.com.

 

Deadline

May 15, 2018

 


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329778617Phoenix-b826b50612018-03-16T00:00:00Production Manager

We are looking for a Production Manager who can lead the planning, setting up and validation of our high-throughput production line. The job will focus on scaling-up the current manufacturing capacity through the installation of a brand-new manufacturing line able to cope with high volume throughput. The candidate will be responsible of managing the budget, interfacing with suppliers, planning and hiring a dedicated team, and managing the whole production plant operations. A strong focus will be dedicated to quality control and process validation activities.

We are looking for an experienced leader in manufacturing operations with a process engineering background that will have a drive to leverage their technical background in a strategic role. The Production Manager will be part of the Danish management team. The ideal candidate has high knowledge about high-throughput manufacturing lines, quality controls, processes validation, microfluidics assembly, biochemistry and reagents quality control, medical device compliance (such as ISO13485), automation, and ideally in injection molding processes.

We are offering an international job within a highly dynamic and fast-growing medTech company with operations in Denmark and Taiwan.

Job description:

  • Responsible for setting up the high-throughput production line of microfluidics consumables in Denmark
  • Responsible for managing suppliers and keep timeline of deliverable of equipment and assembly of the production line
  • Responsible for managing the production department budget in close connection with the CEO
  • Hiring, training, and developing of a highly motivated workforce to elevate the skill level of employees as well as provide flexibility in a multi-functional workforce environment
  • Responsible for managing and maintaining all safety and environmental standards and operating the areas of responsibility within quality, delivery, cost and profit objectives. Lead and manage all resources to ensure the achievement of all KPI’s.
  • Responsible to maximize manufacturing efficiencies consistent with approved quality specifications by developing programs for continuous improvement utilizing the root cause analysis process.
  • Responsible for optimization to reduce cost and to ensure that production flow is up to date
  • Supports quality control programs that are designed to ensure product safety and quality that are consistent with established operating practices.
  • Responsible for defining clear goals and roles to achieve higher performance and output in medium-scale and large-scale production lines.
  • Schedule maintenance requests, equipment shutdowns, and major repairs to maintain production and quality levels.
  • Conduct audits and support the value stream’s position during customer and other audits.
  • Responsible for development of automation processes and quality control processes
  • Responsible for updated production documentation maintenance

 

Qualifications

  • We expect ambitious candidates who have excellent track record of achievements and broad experience in dealing with medical device production processes
  • Proven ability to lead people. Familiarization with the product line and the production processes.
  • Knowledge of budgets, cost analysis, variance analysis, manpower planning, training, project management.
  • Minimum of 3 years of relevant work experience within leadership of manufacturing lines in medical devices and/or other regulated environments (e.g. pharma)
  • Ideally familiar with lean and 5S methodology for production flow
  • English on negotiation level. Knowledge of Mandarin is a plus.

Personal skills

  • Excellent analytical skills and problem-solving capabilities to determine risk assessment
  • Strong drive and willingness to walk the extra mile
  • High degree of dynamic and showing the direction
  • High degree of comfort in working with Asian partners

We offer

  • A challenging and fast-growing working environment with strong Danish-Taiwanese cooperation
  • Co-operation and exchange of ideas within a multinational management/employees company
  • Professional and personal development in scaling a high-tech international company
  • Competitive compensation and benefits

 

How to apply

Please feel free to send a CV and a cover letter to careers@blusense-diagnostics.com.

 

Deadline

May 15, 2018

 

2018-05-11T00:50:26.370 We are looking for a Production Manager who can lead the planning, setting up and validation of our high-throughput production line. The job will focus on scaling-up the current manufacturing capacity through the installation of a brand-new manufacturing line able to cope with high volume throughput. The candidate will be responsible of managing the budget, interfacing with suppliers, planning and hiring a dedicated team, and managing the whole production plant operations. A strong focus will be dedicated to quality control and process validation activities. We are looking for an experienced leader in manufacturing operations with a process engineering background that will have a drive to leverage their technical background in a strategic role. The Production Manager will be part of the Danish management team. The ideal candidate has high knowledge about high-throughput manufacturing lines, quality controls, processes validation, microfluidics assembly, biochemistry and reagents quality control, medical device compliance (such as ISO13485), automation, and ideally in injection molding processes. We are offering an international job within a highly dynamic and fast-growing medTech company with operations in Denmark and Taiwan. Job description: Responsible for setting up the high-throughput production line of microfluidics consumables in Denmark Responsible for managing suppliers and keep timeline of deliverable of equipment and assembly of the production line Responsible for managing the production department budget in close connection with the CEO Hiring, training, and developing of a highly motivated workforce to elevate the skill level of employees as well as provide flexibility in a multi-functional workforce environment Responsible for managing and maintaining all safety and environmental standards and operating the areas of responsibility within quality, delivery, cost and profit objectives. Lead and manage all resources to ensure the achievement of all KPI s. Responsible to maximize manufacturing efficiencies consistent with approved quality specifications by developing programs for continuous improvement utilizing the root cause analysis process. Responsible for optimization to reduce cost and to ensure that production flow is up to date Supports quality control programs that are designed to ensure product safety and quality that are consistent with established operating practices. Responsible for defining clear goals and roles to achieve higher performance and output in medium-scale and large-scale production lines. Schedule maintenance requests, equipment shutdowns, and major repairs to maintain production and quality levels. Conduct audits and support the value stream s position during customer and other audits. Responsible for development of automation processes and quality control processes Responsible for updated production documentation maintenance Qualifications We expect ambitious candidates who have excellent track record of achievements and broad experience in dealing with medical device production processes Proven ability to lead people. Familiarization with the product line and the production processes. Knowledge of budgets, cost analysis, variance analysis, manpower planning, training, project management. Minimum of 3 years of relevant work experience within leadership of manufacturing lines in medical devices and or other regulated environments (e.g. pharma) Ideally familiar with lean and 5S methodology for production flow English on negotiation level. Knowledge of Mandarin is a plus. Personal skills Excellent analytical skills and problem-solving capabilities to determine risk assessment Strong drive and willingness to walk the extra mile High degree of dynamic and showing the direction High degree of comfort in working with Asian partners We offer A challenging and fast-growing working environment with strong Danish-Taiwanese cooperation Co-operation and exchange of ideas within a multinational management employees company Professional and personal development in scaling a high-tech international company Competitive compensation and benefits How to apply Please feel free to send a CV and a cover letter to careers@blusense-diagnostics.com. Deadline May 15, 201811Jobnetb826b506100000000000IDK_OFIR_02DKDanmark228DKK2018-05-10T00:00:0000010EuropaDanmarkEuropaDanmarkSjælland & øerStorkøbenhavnKøbenhavn3139048BLUSENSE DIAGNOSTICS APS11Fruebjergvej 32100København ØDKDanmark0
careers@blusense-diagnostics.comDKDanmarkDKDanmark
8Fuldtid46Permanent541588JobNet47967961000https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=b826b506https://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=b826b506https://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=b826b506&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=b826b506&page=EmailApplyForm&component=SendApplicationButtonhttps://static.matchwork.com/company/logo/DK/ORS/SoMe/Ledelse_og_HR/Ledelse/4.jpgBrænder du for at blive Produktionschef?12007991Dansk3Læse/ tale122222Produktionschef6Ledelse353725424Ina Samuilovacareers@blusense-diagnostics.comDKDanmarkDKDanmark329974953Afdelingsleder til Serviceproduktion ved Region Hovedstadens ApotekRobot Har du et drive for ledelse og optimering og er klar til at spille en central ledelsesmæssig rolle i en GMP-styret produktion, med mange daglige korte deadlines? Hvad søger vi? Vi har brug for en afdelingsleder, der dagligt er aktivt tilstede i produktionen, for at sikre god kontakt til medarbejderne, overblik og den bedste afvikling af den daglige produktion, samtidig med at der er fokus på kundetilfredshed. Du er med hver dag i den daglige drift for at optimere og forbedre flow og arbejdsforhold, til glæde for medarbejdere og kunder. Du bliver en del af et ledelsesteam, der dels er i Serviceproduktionen på den lokale enhed (Herlev eller Rigshospitalet), dels tværregionalt med tilsvarende afdelinger i Region Hovedstaden. Endvidere er du med til at sikre at produktionen efterlever krav til GMP-produktion, såsom hygiejneniveau, dokumentation og oplæring. Du har: produktionserfaring og interesse i at lede medarbejdere i en produktion erfaring med GMP-styret aseptisk produktion en lederuddannelse eller har erfaring fra tidligere lederjob dokumenterede resultater fra et lignende job Du kan: motivere produktionsmedarbejdere, som er på skiftehold være vedholdende mht. at få ting igennem være pragmatisk og udarbejde en vision for din afdeling sætte opnåelige og synlige mål, som følges via bl.a. KPI er Hvem er du? Du er åben, tillidsvækkende og serviceminded, og er god til at formidle viden, strategi og vision, så det giver mening for alle. Du formår gennem værdibaseret ledelse at skabe resultater og forankring af de bedste arbejdsgange, så der bygges bro mellem egen afdeling og hospitalets afdelinger. Du er struktureret, evner at bevare overblik og deltager i den daglige udvikling af produktionen. Du har desuden: et stærkt drive og høje ambitioner lyst til at gøre en forskel i den offentlige sektor interesse for en omskiftelig hverdag med højt tempo og spændende udfordringer Hvem er vi? KFS Serviceproduktionen er en del af Region Hovedstadens Apotek, som er landets største sygehusapotek. vi er organiseret under klinisk farmaci, da vores daglige levering af patientspecifikke cytostatika kemoterapi blandinger sker i tæt kontakt med lægerne og sygeplejerskerne. Produktionen af cytostatika kemoterapi blandinger sker både ved manuel og robot produktion i to-holdsskift på hverdage samt weekend og helligdage. Vi er en engageret medarbejdergruppe på ca. 90 personer, fordelt på laboranter, farmakonomer, farmaceuter, sekretær og hospitalsmedhjælpere. Vi blander årligt ca. 100.000 patientspecifikke cytostatika kemoterapi blandinger incl. til kliniske forsøg. På Region Hovedstadens Apotek arbejder vi målrettet med Eget Ansvar. For os betyder det at både medarbejdere og ledere forpligter sig til at tage ansvar for at hver dag bliver en god dag. Fakta Din daglige arbejdsplads bliver i Apotekets cytostatika produktionslokaler på enten Herlev Hospital eller Rigshospitalet, afhængig af hvor din profil passer bedst. 37 timer per uge incl. frokostpause Flextid 5 uger ferie og 5 ferie-fridage Fordelagtig pensionsordning Løn- og ansættelsesvilkår efter gældende overenskomst med relevant organisation. Kontakt For yderligere information er du velkommen til at kontakte: Enhedschef Charlotte Eland på tlf. 24 7899 57 Afdelingsleder Henrik Bjerring på tlf. 4062 1234 Ansøgningsfrist Fredag d. 5. april 2019 kl. 12.00 Vi holder løbende ansættelsessamtaler.Har du et drive for ledelse og optimering og er klar til at spille en central ledelsesmæssig rolle i en GMP-styret produktion, med mange daglige korte deadlines?

Hvad søger vi?
Vi har brug for en afdelingsleder, der dagligt er aktivt tilstede i produktionen, for at sikre god kontakt til medarbejderne, overblik og den bedste afvikling af den daglige produktion, samtidig med at der er fokus på kundetilfredshed.
Du er med hver dag i den daglige drift for at optimere og forbedre flow og arbejdsforhold, til glæde for medarbejdere og kunder.
Du bliver en del af et ledelsesteam, der dels er i Serviceproduktionen på den lokale enhed (Herlev eller Rigshospitalet), dels tværregionalt med tilsvarende afdelinger i Region Hovedstaden.
Endvidere er du med til at sikre at produktionen efterlever krav til GMP-produktion, såsom hygiejneniveau, dokumentation og oplæring.

Du har:
  • produktionserfaring og interesse i at lede medarbejdere i en produktion
  • erfaring med GMP-styret aseptisk produktion
  • en lederuddannelse eller har erfaring fra tidligere lederjob
  • dokumenterede resultater fra et lignende job
Du kan:
  • motivere produktionsmedarbejdere, som er på skiftehold
  • være vedholdende mht. at få ting igennem
  • være pragmatisk og udarbejde en vision for din afdeling
  • sætte opnåelige og synlige mål, som følges via bl.a. KPI'er
Hvem er du?
Du er åben, tillidsvækkende og serviceminded, og er god til at formidle viden, strategi og vision, så det giver mening for alle. Du formår gennem værdibaseret ledelse at skabe resultater og forankring af de bedste arbejdsgange, så der bygges bro mellem egen afdeling og hospitalets afdelinger. Du er struktureret, evner at bevare overblik og deltager i den daglige udvikling af produktionen.

Du har desuden:
  • et stærkt drive og høje ambitioner
  • lyst til at gøre en forskel i den offentlige sektor
  • interesse for en omskiftelig hverdag med højt tempo og spændende udfordringer
Hvem er vi?
KFS Serviceproduktionen er en del af Region Hovedstadens Apotek, som er landets største sygehusapotek. vi er organiseret under klinisk farmaci, da vores daglige levering af patientspecifikke cytostatika/kemoterapi blandinger sker i tæt kontakt med lægerne og sygeplejerskerne.

Produktionen af cytostatika/kemoterapi blandinger sker både ved manuel og robot produktion i to-holdsskift på hverdage samt weekend og helligdage. Vi er en engageret medarbejdergruppe på ca. 90 personer, fordelt på laboranter, farmakonomer, farmaceuter, sekretær og hospitalsmedhjælpere. Vi blander årligt ca. 100.000 patientspecifikke cytostatika/kemoterapi blandinger incl. til kliniske forsøg.

På Region Hovedstadens Apotek arbejder vi målrettet med Eget Ansvar. For os betyder det at både medarbejdere og ledere forpligter sig til at tage ansvar for at hver dag bliver en god dag.

Fakta
Din daglige arbejdsplads bliver i Apotekets cytostatika produktionslokaler på enten Herlev Hospital eller Rigshospitalet, afhængig af hvor din profil passer bedst.

37 timer per uge incl. frokostpause
Flextid
5 uger ferie og 5 ferie-fridage
Fordelagtig pensionsordning
Løn- og ansættelsesvilkår efter gældende overenskomst med relevant organisation.

Kontakt
For yderligere information er du velkommen til at kontakte:
Enhedschef Charlotte Eland på tlf. 24 7899 57
Afdelingsleder Henrik Bjerring på tlf. 4062 1234

Ansøgningsfrist Fredag d. 5. april 2019 kl. 12.00
Vi holder løbende ansættelsessamtaler.

Region Hovedstadens ApotekHerlev2019-03-15T00:00:002019-04-05T00:00:00
da-DK

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Har du et drive for ledelse og optimering og er klar til at spille en central ledelsesmæssig rolle i en GMP-styret produktion, med mange daglige korte deadlines? Hvad søger vi? Vi har brug for en afdelingsleder, der dagligt er aktivt tilstede i prod...
Indrykket:15. marts 2019
Udløbsdato:5. april 2019