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NMD Pharma A/S

Clinical Supply Manager

Aarhus N

The Clinical Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for all clinical trials.

You must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.

NMD Pharma A/S
NMD Pharma A/S

Senior Data Manager

Aarhus N

The Senior Clinical Data Manager is responsible for leading and overseeing data management activities associated with clinical trials, ensuring data accuracy and consistency, and managing data cleaning and quality control processes.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.

NMD Pharma A/S
A/S Einar Willumsen

Application Specialist – Beverages

Brøndby

Are you passionate about product development within all types of beverages from premium organic CSD's to flavored spirits?

You will work in a high-paced, collaborative and energetic environment optimizing key elements of beverage applications such as taste, stability, preservation and appearance with the goal to design the perfect balance between these elements.

A/S Einar Willumsen
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
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.

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.
Lægemiddelstyrelsen

Dedikeret farmakoepidemiolog til Lægemiddelstyrelsens Dataanalysecenter

København S

Lægemiddelstyrelsen er en helt unik arbejdsplads, i at vi er Danmarks eneste regulatoriske myndighed for lægemidler og medicinsk udstyr. Med denne position følger et helt særligt ansvar, som vi er meget stolte af og bevidste om i vores arbejde.

Dine primære arbejdsopgaver i Lægemiddelstyrelsens Dataanalysecenter er bl.a.:

  • Designe, planlægge og udføre farmakoepidemiologiske analyser på sundhedsdata bl.a. vedr. forbrug, effekt og sikkerhed
  • Udarbejdelse af rapporter, notater og præsentationer til forskellige målgrupper
Gem
R82 A/S

Project Manager

Gedved

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

Kan du samtidig se dig selv som projektleder i en specialiseret verden, hvor innovativt design, teknik og brugervenlighed skal gå op i en højere enhed, så er det dig, vi søger i vores R&D-afdeling i Gedved ved Horsens.

R82 A/S
Phillips-Medisize A/S

Senior Product Test Engineer - Medical Devices

Virum or Struer

Do you want to design safe and reliable medical devices, bringing our clients' life-changing solutions into the hands of patients and helping patients to get better treatment?

You will be an essential contributor in the development and designing optimal verification methods for requirement confirmation.

We seek to enable the best work environment that helps you and the business work together to produce superior results.

Phillips-Medisize A/S
Meliora Bio ApS

QA-assistent med GMP-erfaring

Kalundborg

Vi søger vi en erfaren og selvstændig QA-assistent, der har lysten til at være en del af udviklingen af en nystartet state-of-the-art-bioethanol-produktionsvirksomhed.

Dine primære arbejdsopgaver vil være:

  • Vedligeholdelse af QMS-system, instruktioner, vejledninger osv.
  • Review af batchdokumentation.

Du tilbydes en attraktiv og konkurrencedygtig lønpakke med pension og sundhedsforsikring.

Bavarian Nordic A/S

Utility Engineer

Kvistgård

Er du klar til at blive en del af en innovativ, international vaccinevirksomhed, som den tekniske specialist?

Se video om Bavarian Nordic A/S som arbejdsplads

I rollen vil dine primære arbejdsopgaver være support til teknikere og brugere, herunder hjælp til fejlsøgning på anlæg og udstyr, samt at sikre:

  • Robusthed af anlæg ved kontinuerligt at have styr på vedligehold
  • At GMP og regulatoriske krav er overholdt
Bavarian Nordic A/S
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
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
idoc A/S

Maskinkonstruktør

Vejle, Aalborg eller Albertslund

Brænder du for at arbejde inden for konsulentbranchen med konstruktion af maskiner og anlæg samt bidrage til løbende udvikling og optimering af produkter til vores kunder?

Du tilbydes et udfordrende og spændende job med stor grad af selvstændighed i en virksomhed med højt til loftet og et godt arbejdsmiljø. Du vil få mulighed for at arbejde med forskellige arbejdsopgaver såsom design & udvikling af nye såvel som re-design af eksisterende produkter, projektledelse, samt teknisk dokumentation i et tæt samarbejde med vores kunder.

GE HealthCare Denmark

Technical Writer to GE HealthCare Denmark

Herlev

Join GE HealthCare to help develop high quality instructions for use for our ultrasound scanners, transducers, and reprocessing methods in compliance with rules and legislation in various countries. This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

Our Technical Documentation team consists of six dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities. Our Technical Writers develop and maintain the user documentation for our high-performance equipment.

GE HealthCare Denmark
Gem
Gubra A/S

Scientist for In Vivo Sales in Boston

Boston

Are you passionate about discussing science, identifying opportunities for customer value creation and creating visible results? Do you have excellent analytical skills and a strong commercial mindset? Are you a natural communicator and thrive building relationships? If that is the case, we have a great career opportunity for you.

Your primary area of responsibility will be to partake in day-to-day sales operation, drive the forward-looking dialogues with key customers as well as identifying and following up on new business opportunities. Furthermore, you will be involved preparing sales presentations, market analyses, and marketing materials.

Adding Robotics ApS

Dokumentationsspecialist - Pharma & Automation

Aalborg, Vejle eller Ballerup

Har du lyst til at arbejde med teknisk dokumentation i en bred vifte af automationsprojekter til medicinalsektoren? Så er du måske vores nye dokumentationsspecialist.

Vi rådgiver indenfor automations- og robotløsninger med et særligt fokus på kunder indenfor Health Tech og Pharma. Vi giver dig mulighed for løbende udvikling i en dynamisk konsulentvirksomhed, sparring med mange dygtige kolleger og stor fleksibilitet i dit daglige arbejde.

Radiometer Medical ApS

QA Specialist

Brønshøj

You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.

You will have the opportunity to:

  • Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
  • Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.

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