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Eurofins BioPharma Product Testing A/S

Laborantpraktikant - mikrobiologisk laboratorium

Glostrup

Se video om Eurofins BioPharma Product Testing A/S som arbejdspladsBrænder du for at arbejde med mikrobiologiske og pharmaceutiske analyser og er du klar til at blive en del af et passioneret team?

Vi søger en laborantpraktikant med opstart i september. I vores laboratorium vil du komme til at arbejde med mikrobiologiske og pharmaceutiske analyser og vil gennemgå et spændende, udfordrende og udviklende praktikantforløb. Du vil blive en del af et team med dygtige kollegaer i en virksomhed, hvor kvalitet og faglighed prioriteres højt.

Eurofins BioPharma Product Testing A/S
MagVenture A/S

Teamleder - Final Test and Inspection

Farum

Afsluttende kontrol og sikkerhedstest af alle vores produkter er helt afgørende for at beskytte patienter og brugere. Før afsendelse kontrolleres hvert eneste produkt derfor omhyggeligt for at sikre, at alting fungerer helt som det skal.

Se video om MagVenture A/S som arbejdsplads

I afdelingen Final Test and Inspection vil du derfor ofte være den sidste, der ser produktet, før det tages i brug. Det kræver personer med særlig høj kvalitetssans og et godt overblik. Som teamleder vil du sikre, at afdelingen er velfungerende, og at dine folk trives.

MagVenture A/S
Contura International A/S

Process Supporter – Medical devices

Søborg

You will be part of the production team where you will take a central role in getting Contura products released for the market.

Your strong scientific background will contribute to maintenance and update of the product and process documentation, e.g. process validations, product stability testing reports, risk analysis evaluations, design changes etc.

Your Profile:

  • Civil engineer, chemist, pharmacist, microbiologist or other relevant higher education within natural science
  • Medical device industry experience preferred
Contura International A/S
Pharma4ever A/S

Medical Device & QA-specialist

Ballerup

Brænder du for at gøre en forskel med din QA-ekspertise for vores kunder?

Som erfaren QA-konsulent vil du bruge det meste af din tid hos vores kunder. Vi har allerede en bred vifte af kunder, vi har arbejdet med igennem mange år og der kommer kontinuerligt nye til. Vores kunder fremstiller mange forskellige typer Devices og har brug for vores hjælp og ekspertise til at løse stort set alt inden for QA/RA.

Vi tilbyder dig et fleksibelt og varieret arbejde med de mest spændende virksomheder i branchen. Det giver dig mulighed for selv at planlægge og styre dine opgaver.

Zealand Pharma A/S

GxP Application Manager

Søborg

Currently, we are looking for a new GxP Application Manager, who has experience with maintenance of business applications, user training, stakeholder management and user support.

If this sounds like you, and you are ready to take on a broad area of responsibilities with an independent attitude, you are a match for us.​

You will be System Responsible for our SAS application, the safety database and our Montrium eTMF. You will be part of a fantastic team of other Application Managers and Project Managers, where team work and enthusiasm are buzz words.

Zealand Pharma A/S
Zealand Pharma A/S

Clinical Trial & Senior Clinical Trial Managers

Søborg

In Zealand Pharma we are looking for several Clinical trial Managers/Senior Clinical Trial Managers to join our clinical trial teams as we pursue new and exciting therapeutic areas and optimized ways of working.

In your role as a Clinical Trial Manager, you will play a crucial role in facilitating effective collaboration among essential stakeholders involved in the execution of clinical trials. This includes close collaboration with a Clinical Research Organization (CROs) and internal stakeholders to ensure successful start-up, conduct, and closure of clinical trials.

Zealand Pharma A/S
Contura International A/S

Vigilance (Safety) Associate to join our Clinical and Medical Affairs team

Søborg

As Vigilance (Safety) Associate, you will be joining a company with approximately 100 employees.

Your main responsibilities will include but are not limited to:

  • Data entry and coding of adverse events and technical complaints in vigilance databases
  • Handling of incidents and technical complaints

We all take pride in working efficiently and in an organized manner to meet agreed deadlines, and you will help us maintain a disciplined work environment that allows us to juggle a wide range of tasks.

Contura International A/S
Radiometer Medical ApS

QA Specialist

Brønshøj

The QA Specialist for Radiometer is responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is eligible for a hybrid work arrangement in which you can work part-time at the company location in Brønshøj and part-time remotely from your home.

Radiometer Medical ApS

QA Professional

Brønshøj

You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home.

Gem

Software Team Lead

Farum

We are expanding the company and are looking for an experienced Lead for our Software Team.

Indrykket:
Hentet fra Jobcenter

Equipment Validation Lead

Måløv

Are you ready for a unique opportunity to shape the validation direction for Laboratories of the Future in Novo Nordisk?

Indrykket:

Global Regulatory Affairs Supply Lead - Project Manager

Søborg

Would you like to have the opportunity to work in an innovative and strategic Regulatory Affairs (RA) area?

Indrykket:
Gem

Life sciences CSV consultant with experience in GxP Compliance & Validation

Søborg

Would you like to be part of a fast-growing IT company dedicated to Pharma & Life Sciences?

Indrykket:

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