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Ferrosan Medical Devices A/S

SAP Master Data Specialist

Søborg

Do you want to be a part of Process Support in a company with a unique impact on global healthcare?

You will be coordinating SAP production master data activities throughout the organization in order to achieve safe and predictable product implementation, maintenance, and decommissioning.

Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.

ALK
Gem
ALK

Senior Vice President, Global Chief Medical Office

Hørsholm

We are seeking a highly experienced and dynamic medical executive to join our Global Research & Development organisation in a newly established senior leadership role as SVP, Global Chief Medical Office (GCMO).

In this role, you will act as scientific advisor to the EVP of R&D and the Global R&D leadership team, and your primary objective will be to ensure “one global medical voice” for ALK internally and represent the medical voice of ALK externally.

ALK
Gem
Orifarm

Specialist, Regulatory Affairs (Temporary Position)

Odense S and Søborg

As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.

Further, your main responsibilities include to:

  • Gather information and documentation for variation applications
  • Update dossier sections
Orifarm
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
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
Bavarian Nordic A/S

Professional, Visual Inspection

Kvistgård

Se video om Bavarian Nordic A/S som arbejdsplads

Kunne du tænke dig at være med i et spændende eventyr hos en fabrik i rivende udvikling? Har du erfaring med GMP i lægemiddelindustrien?

Du vil blive en del af Production Support og vil være tilknyttet visuel inspektionsprocessen, hvor du vil være med til at sikre proces, procedurer, GMP og generelle forbedringer på vores proces.

Bavarian Nordic A/S
Gem
CBP A/S

QEHS Koordinator

Vejle

Brænder du for at arbejde med fødevaresikkerhed & EHS (Miljø, Sundhed og Sikkerhed)? Vi tilbyder et udforende og selvstændigt job, med mulighed for at sætte dit eget præg på opgaverne i hverdagen, samt gode muligheder for faglig og personlig udvikling.

Arbejdsopgaver

  • Vedligehold og løbende opdatering af virksomhedens ledelsessystem i relation til BRC-standard, samt Orklas egen standarder indenfor fødevaresikkerhed OFSS og EHS.
  • Være opdateret på og løbende indhente relevant information om lovgivning og standarder.
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.

Pharmacosmos A/S

QA Specialist

Holbæk

We are seeking a competent new colleague to join our QA team in a dynamic and growing company.

You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.

Pharmacosmos A/S
Ferring Pharmaceuticals A/S

Senior Medical Writer

Kastrup

Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?

As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.

Ferring Pharmaceuticals A/S
IFF
Gem
IFF

Creative Assistant

Brabrand

Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?

Your Focus will be:

  • Always following correct compounding procedures
  • Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
  • Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.
IFF
Foodjob Nordic søger for AKV
Gem
Foodjob Nordic

Application Technician – Food Ingredients

Aarhus N

We are looking for an employee with an interest in laboratory and food technology to assist in the AKV FoodLab in Aarhus, where you will become part of the team.

Se video om akv langholt amba som arbejdsplads

Here you will play an important role in relation to taking part in the ongoing laboratory work with a confident and collaborative team approach.

As an Application Technician in AKV FoodLab, your primary tasks will consist of:

  • To assist the Senior Application Specialist with research by running trials of a broad range of applications in the FoodLab and conducting analysis and characterization of food products.
  • Maintenance and cleaning of process equipment.
  • Contribute where required in purchasing tasks for the FoodLab.
Foodjob Nordic
Bavarian Nordic A/S

Laborant til mikrobiologisk team

Kvistgård

Se video om Bavarian Nordic A/S som arbejdsplads

Har du lyst til at være med til at sikre vacciner til forebyggelse af infektionssygdomme?

Bavarian Nordic er i en rivende udvikling og derfor søger vi en laborant til det mikrobiologiske team i Kvistgaard. Du vil i stillingen bidrage til test og frigivelse af vacciner mod kritiske sygdomme. QC-mikrobiologi har ansvaret for at udføre analyser af rutine prøver og valideringer af nye produkter. Desuden yder vi support til vores produktion.

Bavarian Nordic A/S
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
IFF
Gem
IFF

Technical Specialist, Product Quality, Nourish (Maternity cover, 12 months)

Brabrand

Are you an enthusiastic, motivated and detail-oriented professional with a desire to work in a team of colleagues with great technical competencies within production, regulation and processes?

Your core responsibilities:

  • Handling deviations for products manufactured at our factories.
  • Handling of product quality related complaints.
  • Coordinate and implement customer-specific requirements. Maintenance of master data in various IT systems, including SAP.
IFF
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.
Radiometer Medical ApS

Senior Regulatory Specialist

Brønshøj

The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.

If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.

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