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Y-mAbs Therapeutics A/S
Senior Manager/Director of Regulatory Affairs – make your mark on LCM and CMC

Y-mAbs Therapeutics A/S, Hørsholm

Are you ready to take on global regulatory affairs management of products that will have a deep impact on the life of pediatric cancer patients worldwide?

Joining us, you will put your fingerprint on the future structure, procedures and systems of regulatory affairs as we transition from the development stage to a commercial company.

“We offer a flexible environment with a unique combination of scientific insight, entrepreneurship, exciting challenges and with room to be inventive and to find creative solutions to achieve success.” – Rikke V. Oxholm Lillesø, VP of Regulatory Affairs.

Learn more about us and your new role here.

Y-mAbs Therapeutics A/S
LEO Pharma
Principal GLP and/or GCP Auditor

LEO Pharma, Ballerup

As Principal GLP/GCP Auditor, you will represent the Audit function ensuring fulfillment of the Global Audit strategy and contributing to the audit risk assessment oversight within the GLP and GCLP areas. This include audits of non-clinical GLP studies, GLP facility audits, as well as audits of special laboratories and Central laboratories used in Clinical Trials.


You will impact quality within the existing product portfolio as well as our exciting product pipeline where biologics are of growing importance. You will travel world-wide approx. 50 – 60 days a year. Further some of your key responsibilities:

  • Act as Lead Auditor with the authority to assess and influence directly on quality level of non-clinical development activities as well as within clinical trials through audit conduct
  • Expert within GLP/GCLP area with focus on assuring compliance with relevant regulations
LEO Pharma
Afyx Therapeutics A/SHead of CMC

Afyx Therapeutics A/S, Copenhagen

Are you a highly motivated individual interested in a position as Head of CMC in a small, entrepreneurial company offering you a broad range of responsibilities?

As Head of CMC you will be responsible for all Chemistry, Manufacturing, and Controls activities at Afyx from developing the CMC strategy, identifying tasks needed, selection of CMOs and oversight of CMOs. More specifically the following activities will be part of your job description:

  • Identification, selection, and management of Contract Manufacturing Organizations (CMOs) for cGMP process optimization, manufacture, quality control, and supply of investigational medicinal products for clinical trials and commercial products
  • In coordination with Quality Assurance, implement appropriate analytical methods and protocols and ensure that all CMOs are using systems and processes in compliance with relevant regulatory standards and cGMP
Afyx Therapeutics A/SCMC Specialist

Afyx Therapeutics A/S, Copenhagen

Are you a highly motivated individual interested in a position as CMC Specialist in a small, entrepreneurial company with broad responsibility?

As CMC Specialist you will among others be responsible for

  • Support identification, selection and coordination of Contract Manufacturing Organizations (CMOs) for cGMP process optimization, manufacture, quality control, and supply of Drug Product
  • In coordination with Quality Assurance, implement appropriate analytical methods and protocols and ensure that Afyx and all CMOs are using systems and processes in compliance with relevant regulatory standards and cGMP
  • Design of project plans and protocols with internal and external stakeholders
Qiagen GmbhCustomer Solution Manager Infectious Diseases

Qiagen Gmbh

Do you thrive working with sales, science and people and would you like to become part of a small but dedicated team of clinical sales people serving the hospitals and clinical labs in Denmark?

We are a team of sales, support and service people who value a high intensity work day and a relaxed and humorous tone and we are looking for a new colleague.

Your tasks will include:

  • Responsible for sales of QIAGEN clinical product portfolio in Denmark.
  • Develop and execute territory strategy to meet/exceed budget.
  • Work with QIAGEN specialists to achieve sales targets and offer complete solutions to our customers.
Chr. Hansen A/SDevelopment Scientist, 2-year temporary position

Chr. Hansen A/S, Hørsholm

We are looking for a Development Scientist for a 2-year temporary position as soon as possible.

You will be a part of our 13 people Product Design & Application department which is responsible for formulation development, raw material implementation, clinical productions, consumer sample productions, product upscaling and implementation as well as technical production trouble shooting of our probiotic containing solid dosage forms.

For this role, your main tasks will be to:

  • Formulate new products and improve existing formulations of solid dosage forms and liquid based dosage forms
  • Plan, perform and evaluate formulation development activities to cover the requirements of our customers as well as our internal stakeholders
Chr. Hansen A/S
Chr. Hansen A/SDevelopment Scientist

Chr. Hansen A/S, Hørsholm

We are looking forward to have a Development Scientist position replaced as soon as possible. You will be a part of our 13 people Product Design & Application department which is responsible for formulation development, raw material implementation, clinical productions, consumer sample productions, product upscaling and implementation as well as technical production trouble shooting of our probiotic containing solid dosage forms.

Product Design & Application is a part of Human Health Innovation, Chr. Hansen A/S and is located in Hørsholm. In Human Health Innovation we create solutions for our customers based on science.

We offer you a job in Chr. Hansen, Human Health which is one of the market leaders within probiotics for the supplement and special nutrition industries.

Chr. Hansen A/S
Dansk ErhvervFødevarekonsulent

Dansk Erhverv, København

Dansk Erhverv søger en konsulent, som brænder for at hjælpe Dansk Erhvervs medlemmer på fødevareområdet.

Dansk Erhverv søger en ny kollega, der vil arbejde med fødevarelovgivning og hjælpe virksomheder i forhold til krav og regler på fødevareområdet. Jobbet består af at varetage sekretariatsfunktionen for dagligvarehandelens fælles branchekode vedr. overholdelse af fødevarelovgivningen. Derudover skal du også rådgive vores andre virksomhedsmedlemmer indenfor fødevareområdet, bl.a. fødevaregrossister, detailvirksomheder, hoteller, cafeer mv.


  • Sekretariatsfunktion for dagligvarehandelens fælles branchekode
  • Rådgivning af medlemsvirksomheder i fødevarerelaterede spørgsmål, fx mærkning, egenkontrol, hygiejne, fødevarekontraktmaterialer og kemi i fødevarer, økologi, import og samhandel samt tilbagetrækningssager
Novozymes A/STekniker, Fermentation Pilot Plant, Bagsværd

Novozymes A/S

I Fermentation Pilot Plant søger vi en erfaren, dygtig og entusiastisk tekniker til en stilling med spændende udfordringer indenfor udvikling af bioteknologiske gæringsprocesser i et dynamisk og internationalt miljø.

Afdelingen består af 39 motiverede medarbejdere fordelt på teknikere, laboranter og kemikere. Vi arbejder i pilot skala (0,5 - 2,5m3) med gæringsudvikling og processopskalering til produktionssites over hele verden.

Du kommer til at indgå i et teknikerteam på 10 mand med ansvar for at drive vores pilot aktiviteter. Arbejdet foregår på skiftehold med dagvagter og eftermiddagsvagter samt weekendvagt hver 3 uge. Hvert år holdes 3 ugers sommernedluk og vi har også lukket omkring jul og nytår.

Products Support Specialist


Do you have a great amount of knowledge about the health and beauty industry or do you have a background as a pharmacologist, pharmacist, product specialist, biologist, or another similar background? Would you like to use your flair for obtaining in-depth knowledge about a wide range of products and for developing knowledge with others?

s Product Support Specialist, your main responsibility will be to provide information to distributors and customers including answering questions about the science behind Nu Skin's product line and product usage. You will act as main point of contact of Product Support in regional projects and assignments and you will have following responsibilities:

  • Provide qualitative product trainings so that our Customer Service Representatives have relevant and up to date product information
  • Increase Brand Affiliate and customer knowledge through excellent product support
Thermo Fisher Scientific
Senior Regulatory Affairs Specialist

Thermo Fisher Scientific, Roskilde

Exciting new opportunity for a Regulatory Affairs professional to join our small but dedicated Regulatory Affairs team based at our production site in Roskilde, Denmark.

In this role you will provide regulatory affairs support, maintain and update medical device regulatory filing including product registrations, and technical files.

What will you do?

  • Ensure availability of up-to-date Design History Files for regulated products
  • Prepare, submit and manage regulatory filings required for product market approvals as necessary
  • Function as a RA subject matter expert on new product introduction and engineering design control teams
Thermo Fisher Scientific
Dahl & Kjærgaard Human Resources ApSCountry Sales Manager

Dahl & Kjærgaard Human Resources ApS recruiting on behalf of Italy Trade in Copenhagen

Highly experienced within fruit and vegetables

With the capability and the will to make us grow in Denmark and the Nordic Countries

The company is a well-consolidated Italian company who produce and sells products on several markets around Europe - mainly within the FMCG/Retail market as well as on the Foodservice/Catering and the B2B market and they are still expanding.

With a reference to the European CEO and in cooperation with your Scandinavian colleagues and the European HQ, you will establish and develop mainly the Danish market within the areas of FMCG/Retail/ convenience, Foodservice/Catering and the food industry (B2B). As a part of the job you will:

  • Develop and define the market and the strategy and you will implement it
  • Establish and develop our customers
  • Establish, maintain, and develop relations with our customers as well as suppliers
Xellia Pharmaceuticals ApS
Automation Project Manager til Engineering

Xellia Pharmaceuticals ApS, København

Kan du sørge for fremdrift og daglig ledelse af Xellias automationsprojekter? Og kan du rådgive om valget af fremtidige tekniske løsninger?

Vi søger en dygtig og målrettet kollega med viden og erfaring inden for Automation - herunder løbende forbedringer samt strukturering og gennemførelse af automationsprojekter. Du bliver en del af Engineering, som i den kommende tid har fokus på forskellige spændende projekter på siten i København. Vores kunder er også vores kollegaer og vi sætter en ære i at levere en god service på et højt fagligt niveau.Xellia er en specialiseret medicinalvirksomhed, som er førende inden for udvikling, produktion og markedsføring af antiinfektionsmidler.

Xellia Pharmaceuticals ApS
ORANA Denmark A/SQC Online/Packaging Supervisor

ORANA Denmark A/S, Rynkeby

Som QC Online Supervisor hos Orana Denmark får du ansvaret for overvågning af produktions- og forpakningskvaliteten på vores 6 produktionslinjer. Du vil have din daglige gang i produktionen, og overvåge kvaliteten af vores produktionsforløb, samt få ansvaret for kvalitetstjek af indkomne pakkematerialer.

Vi søger en erfaren fødevare-/procesteknolog der, i tæt samarbejde med resten af vores QC-team, kan sikre at kvaliteten af vores produkter lever op til vores specifikationer, kundekrav og høje interne standarder.

Dine ansvarsområder og opgaver:

  • Daglig overvågning og opfølgning på forpakningskvaliteten på alle produktionslinjer
  • Udføre kvalitetsgodkendelse af primære- og sekundære pakkematerialer
  • Deltage i evaluering og optimering af eksisterende forpakningsløsninger – fra primær emballage til færdigpakket produkt
Fertin PharmaSenior Project Manager – Manufacturing & Engineering

Fertin Pharma, Vejle

One of our senior project managers have been given a new opportunity in Fertin Pharma, why we now search for a new senior project manager that will support us succeeding with our ambitious growth strategy.

As senior project manager in Manufacturing & Engineering, you will ensure in-time supply chain capability creation during development of new products. You will be one-point of contact in supply-chain towards R&D in the development phase of new projects and take over the project manager role in the transfer and ramp-up phase of new products. You will become part of our Project Management Office in Manufacturing & Engineering reporting to Senior Manager of Manufacturing & Engineering.

Fertin Pharma
Eurofins Steins Laboratorium A/S
Rådgivere inden for fødevarelovning til Consultancy

Eurofins Steins Laboratorium A/S, Vejen

Vi søger to nye kolleger til afdelingen. En seniorrådgiver med flere års erfaring inden for fagområdet samt en rådgiver der er nyuddannet eller har få års erfaring inden for ovenstående område.

Vi håndterer mange forskellige opgaver i afdelingen og alle ovenstående områder kan komme i spil. Det kan være løsning og udvikling af mærkningsopgaver, herunder at sikre korrekt og lovlig mærkning på fødevarer. Eller du vil kunne komme til at arbejde med risikovurderinger, audits, holdbarhedsforsøg samt andre ad hoc-opgaver alt efter din erfaring og faglige profil. Du vil blive en del af et team på 8 personer, hvor der vil være stor mulighed for at videreudvikle og anvende dine faglige kompetencer.

Eurofins Steins Laboratorium A/S
Arla Foods
Mejerist til skummesalen og proces

Arla Foods, Hobro

Som Mejerist på Hobro Mejericenter kan du se frem til en spændende og udfordrende hverdag blandt 11 gode og glade kolleger.

Da du indgår i en turnusplan i produktionen, skal du regne med at få skiftende arbejdstider. Du kommer til at skulle køre vores mælke-, yoghurt- og skyr-afdeling. Arbejdet kræver at du kan holde et køligt overblik i pressede situationer.

Din arbejdsdag vil bestå af opgaver som at:

  • Arbejde med optimering af vores anlæg
  • Selvstændigt drive og dokumentere produktionen under hensyn til gældende kvalitets forskrifter
  • Opretholde en høj hygiejnestandard
Arla Foods
Fertin PharmaSenior Specialist til Pharma Processupport

Fertin Pharma, Vejle

Fertin Pharma A/S søger en ny energisk medarbejder. Du bliver en del af Manufacturing Engineering Support som består af i alt 14 personer med en teknisk eller akademisk baggrund som supporterer alle produktionens områder. Som Senior Specialist kommer du til at bruge din erfaring med GMP til at sætte det rette kvalitetsniveau for vores produktion af farmaceutiske produkter.


  • Support af vores pharma-produktion i overensstemmelse med gældende myndighedskrav og krav i Fertin Pharma.
  • Ansvar for behandling af komplekse afvigelser og reklamationer, herunder udførsel af systematisk problemløsning, root-cause så problemet identificeres og de rigtige korrigerende handlinger sættes i gang
Fertin Pharma
Ambu A/SStandard Specialist, Global Innovation

Ambu A/S, Ballerup

Do you have experience with standards for medical devices? Do you want to be a part of product development and maintenance? Are you motivated by making a difference for your customers by making sure our products always set and meet the highest level of performance, from a user perspective? Do you want to focus on setting the bar for how to develop sustainable medical devices?

In this newly established and challenging position, you will be an active contributor in the innovation team taking a role as a Standard Specialist. You will be charged with keeping an overview of applied standards across Ambu’s product portfolios, and being Ambu’s representative in European ISO standard committees, helping to shape the future of medical device development.

Xellia Pharmaceuticals ApS
Operatører til API-produktionen

Xellia Pharmaceuticals ApS, København

Vi søger nye kollegaer til API-produktionen i København. API-produktionen dækker både fermentering og oprensning af forskellige non-sterile API’er. Vi søger lige nu operatører til både fermenterings- og oprensningsfabrikkerne, så er du teamplayer af natur og parat til nye udfordringer, så er du muligvis vores nye kollega.

Som operatør vil dine primære arbejds- og ansvarsområder være:

  • Overvågning og betjening af procesanlæg, herunder fermentorer, centrifuger, ionbyttere, osmoseanlæg, HPLC-anlæg og filtreringer
  • Overvågning og betjening af forsyningsanlæg, herunder vandanlæg og nedbrydningsanlæg
  • Arbejde i henhold til GMP-regler efter afdelingens SOP’er
Xellia Pharmaceuticals ApS