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Minerva Imaging ApS

Business Developer with a background in Science

Ølstykke

Do you want to be at the forefront of Targeted Radiopharmaceuticals and Molecular Imaging?

We are looking for a professional Business Developer with a background in life sciences and the ambition to contribute to further strengthening Minerva Imaging as the trusted partner for targeted radiopharmaceuticals and molecular imaging.

What truly matters is your passion for the advancement and know-how of our scientific studies and your ability to foster long-term relationships with our collaborators.

CGI Danmark A/S

Vil du være med til at tegne fremtidens IT-løsninger indenfor Patologi og Genetik?

Tranbjerg

Du får en spændende rolle på tværs af vores produkter i hele Health Divisionen, men i særdeleshed med fokus på løsninger i patologiafdelingen.

Med din baggrund fra laboratorieområdet vil du i høj grad skulle konsultere og rådgive vores kunder, ligesom du bliver ansigtet udadtil på fysiske kundemøder, både opsøgende samt opfølgende. Med din viden vil du være i stand til at analysere kundebehov, for efterfølgende af levere input til en løsningsbeskrivelse.

CGI Danmark A/S
Tetra Pak Processing Systems A/S

Process Engineer

Højbjerg

The Process Engineer will be responsible for process engineering and technical support of Tetra Pak capital projects, as well as specification of equipment and functional design within the given time and budgets.

You should be prepared to travel approximately 30% of your time to meet colleagues, customers and suppliers to fulfil the role (internationally, with extensive travel throughout North Europe & Benelux).

Tetra Pak Processing Systems A/S
Gem
Convatec

Test & Reliability Engineer - Sustaining Engineering, Medical Devices

Lejre

Do you have a keen eye for Physical Testing, Product Quality, Reliability, Validation, and Documentation? Are you looking for an opportunity to merge your passion with our expertise in the Test and Verification of Infusion Care Medical Devices, for the treatment of chronic diseases such as Diabetes and Parkinson’s Disease?

As a Test Engineer, you will be involved in developing and working with a diversity of physical test methods. Planning and coordinating tests in our laboratory in Osted near Roskilde, and partners within Global Convatec and external. Most of your time, you will be part of a project team in SEG.

Convatec
Bavarian Nordic A/S

Manager Virus Production

Kvistgård

Se video om Bavarian Nordic A/S som arbejdspladsDo you want to play a central and important role in Bavarian Nordic´s manufacturing strategy by setting directions and ensuring smooth daily operation in our production facility?

Our newly established Drug Substance Facility in Kvistgaard will soon start production ramp-up, and we therefore need to strengthen our leadership. You will become responsible for the day-to-day shopfloor management of 15-20 operators.

Bavarian Nordic A/S
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
Gem
Cbio A/S

Scientist (maternity leave temp), cell-based immunotherapies

Søborg

Are you enthusiastic about developing next generation cell-based immunotherapies that bring new hope to late-stage cancer patients?

You will help the R&D team in a 6-months temporary position as one of our coworkers is on maternity leave, and will help the team with a possibility for further extension.

We are looking for a person experienced in immune oncology or related area with documented practical experience in cell culture and flow cytometry.

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
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
BioCirc Group ApS

Sales Trader

Middelfart

We are looking for a Sales Trader who will play a vital role in ensuring BioCirc’s ambitious growth plans.

The successful candidate will together with the Portfolio Manager be responsible for the short-term sale of Certificates, optimizing the portfolio, gather market intelligence, and ensuring value added through the whole supply chain of biomethane production, but also new renewable products stemming from our energy clusters.

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.
LGC Biosearch Technologies A/S

Lab Technician

Lystrup

Med laboratorier i USA, Storbritannien, Tyskland og Danmark har LGC Biosearch Technologies planer om at fortsætte med at vokse.

Vi søger i øjeblikket talentfulde kandidater, der er klar til udfordringen med at arbejde i en formålsdrevet organisation med høj vækst.

Du vil blive en del af et mindre team og indgå i produktionen, hvor der syntetiseres, oprenses, analyseres, kvantificeres samt laves QC kontrol af syntetiserede produkter.

Vi tilbyder en arbejdsplads med gode kolleger, højt humør, en attraktiv frokostordning og muligheden for massage, hvis ønsket er der.

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.

Gem
Terma A/S

Specialist in Organic Coating Processes and Chemicals, Materials & Processes Engineering Department, Terma Aerostructures A/S.

Grenaa

Your role involves overseeing all organic coating processes, ensuring compliance and quality of materials such as epoxy- and polyurethane-based paints. You will also manage the requirements for consumable chemicals, like solvents for surface cleaning.

The responsibility furthermore entails the overall responsibility for REACH surveillance and chemical substitution activities at our Grenå manufacturing site, in close collaboration with other process owners.

Gem
Unibio A/S

QEHS Manager

Kalundborg

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

Do you want to help develop the protein of the future, which will make it possible to feed the world's growing population without damaging our ecosystems?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.

Unibio A/S
BioMar Group

Laborant

Brande

Har du øje for detaljen og fokus på kvalitet? Henter du samtidig energi via samarbejde, og kunne du tænke dig at blive vores 6. medlem i vores kvalitetslaboratorium?

Opgaverne omfatter blandt andet:

  • Analyser og kontroller jf. vores kvalitetskontrolplan
  • Support og samarbejde med produktionen
  • Dokumentation og sikring af sporbarhed
BioMar Group

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