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Xellia Pharmaceuticals ApS

Senior Specialist til QC hos Xellia Pharmaceuticals

København S

Drømmer du om mere ansvar, med forskelligartede opgaver, og har du en passion for mikrobiologi? Vil du spille en central rolle i Xellias produktionen af livsvigtig antibiotika?

Som senior specialist vil du blive faglig ansvarlig for vores count release-laboratorie, som bl.a. udfører TVC- og LAL-analyser. Derudover vil du indgå i tæt samarbejde med vores sterile produktioner angående EM, hvor de nye Annex 1-krav stiller øgede krav til vores compliance, som du vil spille en vigtig rolle i.

Xellia Pharmaceuticals ApS
GE HealthCare Denmark

Biocompatibility Specialist

Herlev

We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.

This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.

GE HealthCare Denmark
Orkla Care A/S

Medical Advisor med kommerciel tilgang

Vallensbæk Strand

Har du lyst til at arbejde sammen med dygtige og passionerede kolleger, hvor du kan gøre en stor forskel med dine faglige kompetencer og være en vigtig drivkraft i at udvikle det faglige samarbejde med vores kunder?

Din primære opgave er at rådgive omkring vores produkter i den primære og sekundære sektor. Herunder at opbygge et tæt netværk af relevante health care professionals.

Ferrosan Medical Devices A/S

Training Partner

Søborg

Are you passionate about designing high impact training to improve ways of working?

The role will focus on re-designing the training related to onboarding our professionals working directly with our operation, our Operators, and our Laboratory Technicians.

You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words.

Novozymes A/S part of Novonesis A/S

Technician, EMA Solids Support Team

Kalundborg

Welcome to Solid Support Team 13 skilled process engineers and technicians responsible for quality, introducing new products, throughput, and optimizing the products.

In this role you’ll make an impact by:

  • Responsible technician for the MG-coating line, ensuring smooth and efficient coating processes for granulating with MnTACN
  • Coordinate the steering system changes, bridging the gap between process engineers, technicians, and programmers to optimize operational efficiency.
Arla Foods amba

Associate Sensory scientist/Sensory Panel Lead - Arla Innovation Centre, Aarhus

We are looking for two new Sensory Panel Leads. One new collegue for a 1 year maternity cover and one for a 3 year project. For both positions we hope we will be able to prolong the employment or offer new challenges within Arla Foods.

Your key responsibilities will be:

  • In close contact with stakeholders, guide and choose the proper test-setup to deliver the sensory results needed
  • Panel training and development of panel competences within specific areas of interest
Arla Foods amba
Radiometer Medical ApS

Regulatory Affairs Specialist

Brønshøj

The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.

In this role, you will have the opportunity to:

  • Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
  • Ensure compliance with EU regulations.
  • Generate STED files, international submissions & assess design changes.
  • Plan and execute projects for new regulatory requirements.
Little Green Pharma Denmark ApS

Junior QA Specialist søges

Odense N

Motiveres du af at sikre et godt samspil mellem GMP compliance og den kommercielle drift?

Little Green Pharma er en international medicinsk cannabis virksomhed med hovedkontor i Australien. I vores topmoderne drivhuse i Odense og Perth har vi faciliteterne til at fremstille mere end 23 tons medicinsk cannabis biomasse om året, hvor størstedelen produceres i vores 21.500m2 drivhuse og vores 4.000m2 GMP godkendte produktions-lokaler i Odense, som vi har ambitioner om at vækste over de kommende år til at opnå fuld udnyttelse.

ISG Danmark søger for Persano Group A/S
Gem
ISG Danmark

Fleksibel og nysgerrig QA-koordinator med lederpotentiale

Græsted

Kan du se dig selv stå i spidsen for at sikre høj kvalitet for mere end 1500 forskellige produkter årligt?

For Persano Group søger vi en QA-medarbejder, som kan se sig selv vokse ind i en ledende funktion, og som har den rette mængde af drive, nysgerrighed og ejerskab til at bidrage i en familiedrevet virksomhed, hvor stor passion er den kultur, der gennemsyrer virksomheden.

Gem
R82 A/S

Product Compliance Specialist

Gedved

Ønsker du at arbejde sammen med dedikerede og erfarne kollegaer, der brænder for at udvikle og producere hjælpemidler til børn og unge med funktionsnedsættelse?

Du vil medvirke til at sikre, at de regulatoriske krav til medicinsk udstyr (klasse I) bliver overholdt.

Vi ønsker bl.a. følgende opgaver dækket med vores nye kollega:

  • Ansvarlig for godkendelse af nye produkter sammen med R&D teamet
  • Deltage i nyudvikling herunder udarbejdelse og godkendelse af regulatorisk dokumentation

Som ansat hos R82 er der stor fokus på både personlig og faglig udvikling af den enkelte medarbejder.

R82 A/S
Gem
Convatec

Project Manager - Sustaining Engineering & PMO

Lejre

We are looking for an experienced Project Manager to join our PMO, Technology and Innovation. You will lead sustaining engineering projects with multidisciplinary teams of engineers and specialists.

You will apply your project management, people leadership, and technical skills to qualify and implement changes to existing products e.g., material changes or quality updates. Together with your team you create clear ambitious plans and ensure projects are delivered on time with agreed quality, scope and cost.

Convatec
Radiometer Medical ApS

Regulatory Affairs Manager

Brønshøj

The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.

This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:

  • Ensure regulatory compliance to maintain market approvals
  • Lead a team of skilled RA associates
  • Ensure alignment with relevant stakeholders
Arla Foods amba

Food Technician - Arhus

Are you passionate about turning ideas into concrete products via your hands-on technical skills?

As Food Technician you will be the prime responsible for running pilot scale trial-production of a wide range of dairy/’plant based’ products. Your work will always happen in close collaboration with product developers/food designers. To be more specific, you will:

  • Perform pilot trials within a wide variety of product and technology areas
  • Contribute to the preparation of the test proposal and help plan the trials
Arla Foods amba
Statens Serum Institut

Head of the Department of Virus & Microbiological Special Diagnostics

Copenhagen

Do you have solid management experience and deep insight and experience within virology?

As Head of the Department of Virus & Microbiological Special Diagnostics, you are responsible for the daily management of the department to ensure the diagnostic preparedness for infection in a one-health perspective with synergy between laboratory diagnostics in humans and animals.

Center for Sundt Liv og Trivsel

Center for Sundt Liv og Trivsel søger seniorforsker indenfor graviditet og føtal programmering

København S

Dine arbejdsopgaver bliver blandt andet

  • Du skal lede projekter indenfor før og under graviditet i relation til barnets udvikling, herunder betydningen af biologiske og sundhedsmæssige forhold før og under graviditeten og betydningen af disse for barnets vækst og udvikling.
  • Du skal lede og bidrage til udvikling, planlægning og evaluering af humane interventioner.
  • Du skal lede og bidrage til kvantitative undersøgelser og inddrage kvalitative aspekter.
Center for Sundt Liv og Trivsel

Center for Sundt Liv og Trivsel søger seniorforsker indenfor mandlig reproduktion med kendskab til sundhedsadfærd

København S

Dine arbejdsopgaver bliver blandt andet

  • Du skal lede projekter indenfor mandlig reproduktion med særlig fokus på betydningen af biologiske og sundhedsmæssige forhold før undfangelse og betydningen af disse for barnets vækst og udvikling.
  • Du skal lede og bidrage til udvikling og planlægning af en intervention og andre aktiviteter.
  • Du skal lede og bidrage til kvantitative undersøgelser og inddrage kvalitative aspekter.
IFF
Gem
IFF

Senior Application Specialist - Culinary

Brabrand

For the Culinary Design in Brabrand, we are seeking a Senior Application Specialist to assist us in servicing our external and internal customers.

Main Responsibilities:

  • Servicing our European based customers within the Culinary solutions – from Globals to Start ups
  • Execution of customer related tasks in close collaboration with colleagues in the group and across the entire organization
IFF
Amgen Denmark

Senior Engineer Device Manufacturing

Søborg

Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?

Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.

Gem
Orifarm

QA Specialist og Senior QA Specialist

Odense S

For dig, der trives med at arbejde med kvalitet og lovgivning fra et operationelt perspektiv, både selvstændigt og i dialog med vores leverandører og interne afdelinger.

Som QA Specialist vil du være det koordinerende bindeled mellem de forskellige teams i QA, regulatorisk og Pharmacovigilance i relation til udfærdigelse eller opdatering af eksisterende TA.

Orifarm
Gem
HERAX

Kickstart your career as a Life Science Business Consultant

Gentofte

Looking for the opportunity to combine your interest in life sciences with the business aspects of consulting?

Then grab this career-building chance to work with and learn from talented colleagues as you help digitalize the clinical landscape for clients across the globe.

Not only will you get to hone the skills that will make you a good consultant, but you’ll also get to see the direct impact of your work as you help pharma companies make a difference in patients’ lives

- John Aggerholm, Project Director
HERAX

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