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QA Assistant, GS-5, QAC

This position is embedded in the Quality Assurance Centre (QAC), where teams have coreresponsibilities around quality assurance and quality control of supply processes and the productswe procure and deliver.

The incumbent will beresponsible for assisting the Quality Assurance Specialist (non-pharma) in the management of all aspects of Pre-Delivery Inspection (PDI) arrangements for non-pharma items from initial request tofinal invoice certification.

Laborant

Hos os kan du udvikle dig i en af verdens største og mest ambitiøse laboratorievirksomheder, hvor du kan gøre en forskel i en spændende hverdag.

Du vil få rigtig mange prøver gennem hænderne, hvor du i trygge rammer vil blive grundigt oplært til at udføre forskellige metoder.

Dine daglige opgaver vil primært bestå af:

• Neddeling af prøver
• Forberede standardrækker og kontroller
• Ekstraktion, eluering etc.

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.

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.

Farm Sustainability Manager - Aarhus

Do you have insights in agrobiology, biodiversity and a beating heart for nature and dairy?

In this role you will be the center of knowledge sharing among our farmer owners and a lighthouse for inspiring to sustainable actions focusing on crop nutrition, soil, natural areas and biodiversity.

You will facilitate meetings to inspire farmer-owners to investigate and make climate actions and become a relevant part of the strategy at farm level.

Project Manager PMO - Medical Devices

We are looking for an experienced Project Manager to join our Technology and Innovation PMO organisation.

You will lead multidisciplinary teams of engineers and specialists, applying your project management, people leadership, and technical skills to develop new products, variants or upgrades.

Senior Regulatory Affairs Manager

This pivotal role will involve navigating the complex regulatory landscape associated with technologies for the production of hydrogen, its derivatives and other related technologies. This critical role will also involve ensuring compliance and strategically influencing regulatory development to support our mission.

The ideal candidate will have a deep understanding of energy regulations, a passion for sustainability, and the expertise to guide our company through the evolving regulatory environment.

EHS Team Lead

The HSE Team Lead will report directly to the Head of HSE and will serve as the direct supervisor for a team of 8 skilled HSE professionals, comprising 4 HSE Officers and 4 Workflow Managers. This team is characterized by its dedicated members who excel in collaboration, mutual support, and fostering strong relationships with production teams.

As the Team Lead you will ensure that the team delivers high-quality work aimed at enhancing the factory's safety culture and preventing accidents.

Sales Manager - Personal Care

Do you thrive on building good relations to customers and partners? And on using your technical skills to provide the best solution for the custumer?

CosTech Chemicals ApS is known in the industry for being an advisor with a service-provider approach and do not act as “chemistry pushers”. As such the right candidate is good at creating strong and lasting relations to customers and partners and have a background within chemistry or equivalent.

Nordic Account Manager

In the exciting role as Nordic Account Manager, you will work with SSI Diagnosticas full product portfolio and sales towards the clinical and industrial segments in the Nordics.

You will work with a lot of talented and engaged colleagues and will be a key player in developing and grow the Danish market. You will be working closely together with other Nordic sales reps, customer service and relevant colleagues from our production and trade product partners.

Sensory Scientist - Sensory & Consumer Science team - Aarhus

Are you ready to join the highly ambitious Design & Connect team in Arla’s Global Innovation Centre in Skejby?

You will be key in delivering sensory insights and recommendations to both innovation and business. Doing so, you will work closely with product designers and consumer scientists on the product experience, and scientists and stakeholders across the organization.

Industrial Postdoc – Multisensory Communication Behaviour

We are seeking an industrial postdoc candidate to join our scientific team. We are looking for a highly motivated and skilled candidate to carry out independent research within multisensory communication behaviour.

Your work with us will have the potential to provide ground-breaking advantages in user benefits in hearing healthcare.

Laborant QC Sampleflow

Har du laboratorieerfaring og kunne du tænke dig at tage det næste skridt i din karriere?

Du får ansvar for og stor medbestemmelse over dine opgaver så de fleste dage vil gå stærkt, og opgaverne bliver ofte andre end dem, du havde planlagt og forventet.

Du vil opleve en dynamisk og udfordrende hverdag i QC, med mange spændende opgaver og en åbenhed over for nye idéer.

Project Coordinator

Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?

As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.

Clinical Supply IRT/RTSM Specialist

Come help us deliver high-quality clinical trial supply to trials all over the world

We are looking for an IRT/RTSM specialist to help us ensure timely setup of IRT/RTSM systems to support the delivery of trial supply for Ferring clinical programs globally.

In this role you are expected to not only collaborate closely with cross-functional teams but also contribute to a knowledge-sharing mindset and promote a collaborative and innovative work environment. You must have a flair for respectful communication with a range of stakeholders such as Clinical Operations, IT and Quality Assurance.

Operations Data Coordinator for Drug Substance Production

The primary task within the position is to collaborate with various departments (e.g., automation, tech transfer, and manufacturing departments) to collect and translate information required for building efficient production campaigns and daily task schedules.

You will be part of a team with a great sense of humor and a high willingness to support where needed.

QA Specialist for Environmental Support

In this role, you will join Bavarian Nordic's QA Organization as a QA Specialist tasked with establishing strong relationships with stakeholders, effectively communicating GxP requirements, and handling crucial Quality Events in the Quality Management System (QMS).

This is in the context of environmental monitoring, aseptic performance, and sterile & low bioburden processes in Drug Substance and Drug Product Production. Additionally, you will contribute to the ongoing improvement of QA processes to elevate overall quality standards.

2 Regulatory and Marketing Compliance Managers

Har du interesse for og meget gerne erfaring med Regulatory Affairs – og helt optimalt med Marketing Compliance – og vil du gerne arbejde mere målrettet med Marketing Compliance?

Dine arbejdsopgaver bliver bl.a.:

• Compliance review af marketingaktiviteter og -materialer for den farmaceutiske industri og anmeldelser til Etisk Nævn for Lægemiddelindustrien
• Oversættelser af regulatoriske og medicinske dokumenter (dansk/engelsk)
• Andre regulatoriske opgaver svarende til opgaverne i et dansk datterselskab: gennemgang og opdatering af produktinformation, regulatorisk review af artwork m.v.

Senior Process Specialist

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.

Projektleder til Miljøvurdering og Anlægsprojekter

I rollen som projektleder til miljøvurdering og anlægsprojekter vil du primært skulle udarbejde screening og miljøvurderinger for vores anlægsprojekter. Du får ansvaret for at bidrage med faglig viden, udarbejde miljøvurdering og gennemfører mindre anlægsprojekter. Du vil være en vigtig sparringspartner for dine kolleger og sikre kvalitet i alle led af processen.

Når du bliver en del af vores team, træder du ind i en behagelig arbejdsplads, hvor respekt, ordentlighed, humor og godt humør er nøgleord. Vi tilbyder en fleksibel arbejdsplads, hvor der er mulighed for hjemmearbejde.

Scientist for Biomarker Assays

Are you eager to use your scientific skills and expertise in preclinical research?

As our new scientist, your tasks will include:

• Coordination and support of biomarker experiments, including supervision of lab technicians.
• Perform data analysis, interpretation, review, and reporting of study results.
• Development of new biochemical- and immunoassays and troubleshooting of existing assays.