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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
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
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
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
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.

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
Gem
AB Neo A/S

Ruminant Nutritionist – Calf and Lamb Milk Formulations

Videbæk

This is an great opportunity to join our international team that continues to invest in the Ruminant offering looking at way to innovate and enhance our formulations, and additives that support the needs of young animals with some other responsibilities such as:

  • Supporting R&D activities, including feed material and product evaluations, trials, and commercial interpretation and communication.
  • Develop technical ideas to add value to product sales and marketing.
AB Neo A/S
Gem
AB Neo A/S

Health, Safety and Environment (HSE) Manager

Videbæk

Are you a seasoned Health & Safety professional seeking an opportunity to thrive in a supportive and dynamic environment?

We have an exciting opportunity to recruit a Health & Safety Manager, you will play a crucial role in maintaining and enhancing the safety standards at our facility. Your responsibilities will include designing training programs, conducting risk assessments, identifying, and controlling hazards.

AB Neo A/S
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
Gem
Carlsberg

Craft Brewer

København V

Se video om Carlsberg som arbejdspladsEr dit drømmejob at lave innovative øl af de bedste råvarer i et lille og dynamisk team, i tæt samarbejde med forskere? Og matcher du de fleste af nedenstående kvalifikationer?

Ansvarsområder

  • Brygning, gæring, tørhumling, filtrering og rengøring på semiautomatiske anlæg
  • Tapning på dåser og forskellige fustager på semiautomatiske anlæg
Carlsberg
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
Bavarian Nordic A/S

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

Se video om Bavarian Nordic A/S som arbejdsplads

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

Bavarian Nordic A/S

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