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Specialist, Regulatory Affairs (Temporary Position)

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

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

Laborant - AKAFA, Svenstrup

Til laboratoriet på Arla Foods AKAFA i Svenstrup søger vi en dygtig og engageret laborant til en fuldtidsstilling.

Dine primære opgaver bliver kemiske/fysiske og bakteriologiske analyser på halvfabrikata, færdigvarer og ingredienser. Derudover deltager du i en række analyser for produktionen, såsom hygiejnekontrol af produktionsområder, titrering af CIP-væsker, desuden fremstilling af substrat og diverse ad hoc-opgaver.

Regulatory Affairs Specialist

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.

Senior Regulatory Specialist

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.

QC Laboratorie Supporter (Barselsvikariat 12 måneder)

Vi søger en person med det rette servicegen og energi, og som forstår kravene i et cGMP QC-laboratorium. Som vores kommende kollega er det vigtigt at du har forståelse for arbejdet i et laboratorie, er indforstået på en travl hverdag med skiftende prioriteringer.

Er det lige dig vi står og mangler, så kan vi tilbyde dig et spændende og udfordrende job i en virksomhed der går en spændende fremtid i møde med mange nye kunder og produkter og store muligheder for personlig udvikling og ansvar. Dette er en tidsbegrænset stilling, men vi udvider og vækster hele tiden så hvem ved hvad fremtiden bringer?

Laborant med fokus på kvalitet - Slagelse

Vil du være en del af et mejericenter i konstant udvikling, hvor du varetager en nøglerolle og er med til at kvalitetssikre vores produkter?

Som laborant vil du få en vigtigt rolle på vores laboratorium, hvor vi sikrer at kvaliteten af vores produkter altid lever op til både myndighedernes og Arla Foods høje krav. Vores primære opgaver er at udarbejde kemiske-, fysiske- og bakteriologiske analyser på halvfabrikata og færdigvarer.

Teamleder til Laboratorium, HOCO Mejeri - Holstebro

Vil du være med til at sikre optimal udnyttelse af mejeriets linjer og god leveringsevne til kunderne?

I tæt samarbejde med laboratoriets øvrige medarbejdere vil du være ansvarlig for, at analyserne udføres korrekt og til rette tid. Du er være sparringspartner for udvikling af analysearbejde i både laboratoriet og produktionen. Du har det daglige ledelsesansvar og sikre at de rette kompetencer og ressourcer er tilstede for at sikre for at opnå de fastsatte mål. Sikkerhed er vores højeste prioritet, og det er derfor vigtigt, at du går forrest og sørger for, at effektivitet og udvikling foregår i et godt fysisk og psykisk arbejdsmiljø.

Regulatory Affairs Manager

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

Craft Brewer

Er 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

HSE Specialist

As an HSE Specialist, you will have the opportunity to develop and implement safety policies and procedures, conduct training sessions, and ensure compliance with local, state, and federal regulations.

In joining our team, you'll have the opportunity to make a significant impact, ensuring the safety and well-being of our workforce while contributing to our continued success at Duferco Danish Steel.

Product Portfolio Manager, Arla Foods Ingredients - Aarhus

Together with the rest of the team you will make raw material scenario analyses and identify potential challenges to have a fact-based discussion and enable better decision-making.

In short, your responsibilities and tasks include:

• Become a trusted portfolio partner to the commercial organization
• Provide raw material priority recommendation in S&OP and other key-forums

Senior Technical Writer - Regulatory (CMC)

You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.

Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.

MS&T Program Manager

We are looking for an experienced professional from the pharmaceutical industry, who can effectively manage project plans across multiple entities and lead cross-functional processes within our own sites and supply chain.

As a MS&T Program Manager, you will be responsible for managing the projects, maintaining project databases, as well as ensuring effective communication and timely achievement of milestones.

Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)

Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!

As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.

PhD scholarship in Applied Stem Cell Cultivation – DTU Bioengineering

This is a perfect position to make your mark in the stem cell field. The project topic is scalable stem cell manufacturing, specifically for the production of stem cell derived NK cells. This is currently a major bottleneck preventing affordable access to novel stem cell based therapies.

It is a 3-year PhD position in the DigitSTEM initiative: A four-year research collaboration between The Technical University of Denmark (DTU), The Novo Nordisk Foundation Center for Stem Cell Medicine (renew) at University of Copenhagen, and Bioneer A/S that aims at developing new in vitro disease models and cell therapies using human induced pluripotent stem cells.