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Y-mAbs Therapeutics A/S
QA Specialist, GMP QA

Y-mAbs Therapeutics A/S, Hørsholm

Y-mAbs Therapeutics A/S is looking for a QA Specialist, GMP, who will report to Sr. Director, Quality Assurance and be part of a rapidly growing team of highly qualified and motivated colleagues.

It is our expectation that this person will actively contribute to the quality oversight of contract manufacturing activities with commercial products and IMPs; support the Qualified Person(s) by reviewing the product batch documentation and other GMP records; handle deviations, changes and complaints; ensure GMP compliant documentation management.

The position can give great opportunities for further professional development.

Y-mAbs Therapeutics A/S
A/S Orthana Kemisk Fabrik
Procesoperatør/Industrioperatør

A/S Orthana Kemisk Fabrik, Kastrup

Kunne du tænke dig at være en del af en velfungerende fabrik med 28 ansatte i et godt og tæt arbejdsmiljø? Så er du måske vores kommende kollega.

A/S Orthana Kemisk Fabrik søger en kvalitetsbevidst person, som ønsker at være en del af en dynamisk gruppe, og som sætter en ære i at levere et godt stykke arbejde. Som operatør skal du deltage i den daglige produktion af proteiner, peptider og enzymer ud fra animalske råvarer.

Du må gerne være uddannet procesoperatør/industrioperatør eller med faglig baggrund i levnedsmiddelbranchen evt. håndværksmæssig baggrund. Du har muligvis praktisk hands-on erfaring med klassiske vandbaserede biokemiske processer, filtrering, op-koncentrering (inddampning/membranfiltrering), og spraytørring.

Amgros I/S
Udbudsspecialist

Amgros I/S, København

Skal din erfaring med udbud og kategoristyring skabe mere sundhed for pengene? Hvis du har evnen til selvstændigt at varetage dine kategorier – fra kategoristrategi til implementerede rammeaftaler – kan du som udbudsspecialist i Amgros være med til at gøre en reel forskel og skabe mere sundhed for pengene.

Som udbudsspecialist i Amgros bliver du ansvarlig for at gennemføre udbud af rammeaftaler på lægemidler til de danske sygehuse. I rollen indgår således både analyse, strategi, udbud, implementering samt opfølgning på de opnåede resultater i tæt samarbejde med interne og eksterne stakeholders.

Du bliver således ansvarlig for at planlægge, prioritere og styre end-to-end udbud baseret på din kategoristrategi, ligesom du bliver ansvarlig for at facilitere udbudsprocessen inden for de juridiske rammer, og sikre høj compliance og gevinstrealisering på området.

Amgros I/S
Nykode A/SRegulatory Lead

Nykode A/S, Oslo

Our team is now looking for a Regulatory Lead who will serve in the project team for a Nykode project in early clinical development.

The individual will lead, initiate and drive the many regulatory activities, including clinical trial applications and agency interactions and act as an active member of relevant clinical teams. You will ensure high quality documentation in regulatory submissions such as clinical trial applications, IND submissions, and meeting briefing packages and effectively manage associated timelines.

The responsibilities include:

  • Developing and executing sound and robust global regulatory strategies, plans, and activities for Nykode’s products
  • Actively participating in project teams and relevant trial teams
  • Leading and coordinating regulatory activities with Regulatory CMC, documentation specialists, and relevant other internal and external parties Providing input and support to Quality, Preclinical, and Clinical activities and plans
Nykode A/SRegulatory documentation Specialist

Nykode A/S, Oslo or Copenhagen

Our Medical team at Nykode is looking for an individual to join as Regulatory Documentation Specialist in either Oslo or Copenhagen.

The role holds a pivotal role for the regulatory team by being responsible for key administrative tools and documents as well as process optimisation related to regulatory activities and oversight.

The responsibilities of this position include:

  • Assist the regulatory team in preparing and coordinating regulatory submissions such as clinical trial applications, IND submissions, orphan and paediatric submissions, Health Authority meeting requests and briefing package submissions in collaboration with clinical CRO’s and regulatory vendors (e.g. eCTD publisher)
  • Provide support to regulatory submissions, including coordination of review and finalisation of documents across functional areas
  • Manage certain outsourced regulatory activities, e.g. in connection with eCTD compilation
Danpo A/S
Kvalitetsassistent til Danpo, Farre

Danpo A/S, Give

Dine primære arbejdsopgaver vil være support til produktionen og håndtering af afvigelser.

Stillingen indebærer meget tilstedeværelse i produktionen, kombineret med en smule administrativt arbejde, hvilket du skal være indstillet på.

Du vil således bl.a. komme til at arbejde med:

  • Behandling af interne/eksterne afvigelser inkl. løbende forbedringer og support til produktionen
  • Prøveudtagning
Danpo A/S
KLIFO A/S
KLIFO is looking for a Clinical Supply Manager for our Glostrup office

KLIFO A/S

Would you like to use your solid experience within the pharmaceutical industry to join our highly skilled Clinical supply department as Clinical Supply Manager?

We are growing and we need more dedicated colleagues to help us maintain and further develop our high quality level to meet client and own requirements.

As Clinical Supply Manager you will be working with a diversity of tasks from planning and coordinating clinical trials in close dialogue and cooperation with our clients. Preparation and approval of labels texts according to Annex 13, packaging materials, designs and blinding setups, coordinating return & destruction of IMP and cooperate with our distribution team in preparing distribution set ups.

KLIFO A/S
Statens Serum InstitutAfsnitsleder til Statens Serum Institut, TestCenter Danmark - NAT

Statens Serum Institut, København

Har du erfaring som leder af en produktionsenhed eller et laboratorium, og brænder du for at skabe et driftssikkert og agilt laboratorie? Trives du i et dynamisk miljø med stort ansvar og fokus på kvalitet? Så er du måske vores kommende afsnitsleder i TestCenter Danmark i København.

Vores afdeling består af ca. 200 medarbejdere herunder laboranter, assistenter, vikarer, studerende, akademikere, plannere og ledere. Ledelsen af vores laboratoriepersonale (ca. 160 medarbejdere) deles af fire ledere, og denne stilling vil bringe det op til fem ledere.

Du vil få ansvaret for personale, planlægning, sikkerhed og drift af laboratoriet i samarbejde med de andre ledere. Som leder skal du desuden kunne tage systematisk fat på de problemstillinger der opstår og meget gerne bruge værktøjer fra LEAN-kassen til løsningen.

Novozymes A/SSenior Global Claims Process Lead, Regulatory Affairs, Bagsværd

Novozymes A/S

Are you driven by bringing business strategies to life by tailored processes for claims development and intelligence - and continuous improvement of the regulatory deliverables? Then you may have found the right role.

As Senior Global Claims Process Lead you will be part of the Global Regulatory team and work closely with especially our regulatory product experts and the Strategic Opportunity Areas (SoAs), transforming your strong scientific skills to secure operational excellence and high quality deliverables. You will be responsible for coordinating and compiling the relevant assessments and secure a high level of knowledge sharing, sparring and continuous improvement. You will be a member of relevant cross-functional groups and maintain close interaction with stakeholders many parts and levels of the organization, i.e. R&D functions, sales, marketing, intelligence etc.

Ferrosan Medical Devices A/SLabelling Specialist

Ferrosan Medical Devices A/S, Søborg

Do you want to help create and update medical device labels of a product portfolio that helps patients globally?

At Ferrosan Medical Devices, our Product Development department is continuously working to improve processes and adapt to new challenges – and we hope that you want to join us on this journey.

As a team, we work hard and with dedication to deliver holistic support as we:

  • Define technical requirements for the product documentation in accordance with design control
  • Handle the design control, biosafety and product labelling as we ensure the preparation of design input and outputs as well as design verification and validation
  • Prepare the necessary technical evidence, rationales and data to ensure that the product design meets the required functionality, efficiency and safety of our Class III products
Ferrosan Medical Devices A/SLead Auditor

Ferrosan Medical Devices A/S, Søborg

Do you want to lead the auditing processes of our entire medical device company? Can you ensure organised planning and beneficial collaboration to deliver life-saving haemostatic products?

Then join Ferrosan Medical Devices as our next lead auditor and help us improve our self-inspection and external audit programs.

As our lead auditor, you will be responsible for planning and executing audits and potential follow-ups. You orchestrate all phases of our self-inspections and external audits of our CMOs and suppliers, from planning to execution and follow-ups – a task you will be able to set your own personal mark on.

LundbeckSenior Manager Chemical Manufacturing

Lundbeck, Lumsås

Hr du erfaring indenfor ledelse og optimering af produktion? Så har vi måske drømmejobbet til dig på Lundbecks syntesefabrik i Lumsås, Nykøbing Sjælland, hvor vi fremstiller aktive lægemiddelingredienser under GMP-styring.

I forbindelse med en styrkelse af vores organisation, søger vi en Senior Manager til vores produktionsafdeling. Vi har i alt 5 fabrikker på sitet, hver med en teamleder og op til 20 operatører. Fabrikkerne arbejder 2-holds skift dag/aften, man-fre.

I samarbejde med vores nuværende Senior Manager, der har ansvaret for de øvrige 3 fabrikker på sitet, vil du skulle stå for prioritering af opgaver og ressourcer på tværs, så vi møder produktionsmålene og de udfordringer der hører med.

DANISH CROWN A/S
Danish Crown Graduate Programme

DANISH CROWN A/S, Randers

Do you see yourself in a leadership role? Our Graduate Programme is your career kick-starter into a leadership role within Danish Crown. Join a motivated, informal, and result-oriented culture with global career opportunities.

Through hands-on experience and pre-leadership training, you will sharpen your business understanding and improve the qualities needed to become a leader.

You will also attend regular training and workshops with your fellow graduates to improve your abilities within areas such as project management, presentation techniques, lean-thinking, supply chain and group dynamics.

DANISH CROWN A/S
LEO Pharma
Clinical Vendor Manager / Outsourcing Manager

LEO Pharma, Ballerup

If your area of expertise is vendor/outsourcing management within clinical trial development, and you are looking for a job with high level impact and freedom to operate, this job is right here. LEO Pharma has set the ambitious goal to become the world’s preferred dermatology care partner. A cornerstone in making this vision come true is our collaboration with CROs and CMOs on execution of our clinical trials.

LeoPharma

In this position you will get the opportunity to both influence our overall outsourcing strategy and direction for the area and manage partnerships as well. And you will do it together with skilled and dedicated colleagues in a very well-functioning team with offices in Denmark and the US.

Your overall focus is to ensure that we have the best possible vendor set up with the right processes, systems and good relations to stakeholders internally and externally.

LEO Pharma
LEO Pharma
Global Stakeholder Partnership Manager

LEO Pharma, Ballerup

If you are looking for an opportunity to help people worldwide suffering from dermatological diseases, this may be your next position!

The Global Stakeholder Partnership team belong to a highly motivated team of Medical Affairs staff with clinical, research and marketing experience. The role entails strategic partnering within interdisciplinary project teams and the main responsibilities for the position include the ability to provide stakeholder engagement input to strategic plans such as lifecycle plans and strategic launch plans.

LeoPharma

The Global Stakeholder Partnership Manager will be responsible for acquiring, maintaining and expanding knowledge and expertise in relevant stakeholder engagement initiatives. By working closely with dedicated Medical Affairs staff in Regions around the globe, the Global Stakeholder Partnership Manager suggest, develops and support medical affairs activities and encourage best practice sharing.

LEO Pharma
AGC Biologics A/S
Senior Manager

AGC Biologics A/S, Søborg

The Senior Manager (PMO) is responsible for leading a team of Project Managers (5-9 direct references) and their associated Contract Development and/or Manufacturing projects at AGC Biologics, Copenhagen. The role provides direction for the program and portfolio, supporting project controls and timeline management across internal functional and organizational lines as well as with our clients.

Responsibilities:

  • Provide the Project Managers with the necessary program direction for planning, organizing, developing and integrating projects across multiple functional areas.
  • As a people leader, effectively utilize influence and leadership principles to guide and motivate the PM team.
  • Support the Project Managers in aligning expectations and obtain support from the internal functional areas to support the projects
AGC Biologics A/S
KARSBERG – rekruttering og headhunting
Teknisk stærk Project Sales Manager til pharma-området

KARSBERG – rekruttering og headhunting søger for LSS A/S i Randers

Vil du være med til at sælge markedets bedste løsninger?

Som Project Sales Manager indenfor pharma-området og med reference til CEO bliver du en del af en flad organisation, hvor fokus er at skabe vækst og resultater gennem et særdeles stærkt og kompetent salgsteam.

Dit fokus vil være at videreudvikle på salg til eksisterende kunder samt sælge til nye kunder. Salget til nye kunder sker gennem indkomne leads fra marketing samt kundehenvendelser fra interesserede potentielle kunder.

Salget gennemfører du i tæt samarbejde med det tekniske team, som assisterer dig i forbindelse med løsningsforslag og tekniske specifikationer m.m.

Ud fra dine gode relationer og forståelse af kundernes situation, afdækker du deres behov og udarbejder kalkuler og tilbud samt driver selv opfølgning på kunder og tilbud mv.

KARSBERG – rekruttering og headhunting
ALK
ALK søger en Operatør i API Produktion, som har lyst til at gøre en forskel for mennesker med allergi

ALK, Hørsholm

ALK er verdensledende indenfor allergivaccination, og vi er på en utrolig spændende rejse, hvor vi konstant udfordrer og flytter grænserne inden for allergibehandling. Har du lyst til at være med på rejsen, så er det nu, du skal søge stillingen som operatør i API Produktion i Hørsholm!

Som operatør hos os kommer du til at indgå i en større afdeling bestående af kemikere, supportere og operatører, hvis funktion er oprensning af proteiner fra ekstrakter af naturlige råvarer fra husstøvmider og pollen til produktion af allergivacciner i tabletform til allergipatienter. Jobbet som operatør i API Produktion er et afvekslende job, da vi håndterer mange forskellige enhedsoperationer såsom ekstraktion, filtrering, ultra-/diafiltrering mm. Vi sikrer selvfølgelig den nødvendige oplæring, og du vil i høj grad være med til at sikre et godt samarbejde på tværs i ALK!

ALK
Foodjob Nordic
Technical Sales Manager – Food Ingredients

Foodjob Nordic, Herlev

Foodjob Nordic is searching for an experienced Technical Sales Manager for EUROGUM A/S, part of the family owened company Bang & Bonsomer since Spring 2021. In this position, you are responsible for international customers both directly and via the company’s sales offices or distributors.

Foodjob Nordic

In this position, you are responsible for international customers both directly and via the company’s sales offices or distributors. The right candidate has a strong drive and is a self-starting business professional with excellent communication skills, and experience within the European food industry.

Foodjob Nordic
AJ Vaccines A/SProject Manager with GMP knowledge

AJ Vaccines A/S, Copenhagen

We are looking for a Project Manager (PM) to support our project portfolio in Finished Products. You will have the opportunity to work with very diverse projects across our department. The department handles everything from Media production, aseptic formulation, filling to inspection, and packing of our products.

As a PM your overall responsibility is to lead our department projects and activities. Your reporting into steering groups and to management will be an essential part of the decision-making for the projects going forward.

As a PM you will:

  • Handle business cases and project one-pagers
  • Obtain quotes and communicate with external suppliers
  • Manage projects and project groups