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Training Partner

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.

Senior Project Manager

Are you motivated by being the driver of the implementation of new equipment/facilities or complex upgrading projects) up to EUR 15 million?

You will be responsible for and ensure project execution of all phases in your projects including scope definition, identifying the solution, and mitigating risks, time, budget, and quality. We primarily work with the stage gate model for our larger projects.

Ingeniør til validering

Vi har brug for en konsulent til et spændende job indenfor kvalificering og validering. Stillingen byder på mange forskellige opgaver og projekter hos vores kunder på det meste af Sjælland, og du får en spændende, travl og varierende hverdag.

Du vil bl.a. koordinere, planlægge og udføre validerings- og kvalificeringsprojekter, som kan omhandle: rengøringsvalidering, sterilisationsprocesser, procesanlæg, IT-validering, klimafaciliteter, produktions-, måle- og laboratorieudstyr.

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

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.

Validation Engineer

We are looking for a new Validation Engineer, to join the department Validation Engineering of 4 dedicated employees supporting innovation projects and capacity increase projects.

As our new Validation Engineer, you will be responsible for validation and qualification of processes and equipment. You will be working closely with a dedicated project team, throughout the duration of the project lifetime (typically 9-18 months).

Validation Engineer

We are expanding our Validation Engineering Team and are looking for 3 new Validation Engineers, to join the department Validation Engineering of 5 dedicated employees supporting innovation projects, capacity increase projects and customer projects.

As our new Validation Engineer, you will be responsible for validation and qualification of processes and equipment related to customer projects. You will be working closely with a dedicated project team to ensure progress of customer projects.

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.

Administrativ laborant

I prøvemodtagelsen registreres alle laboratoriets prøver, kemiske såvel som mikrobiologiske. Der er i prøvemodtagelsen ikke noget analytisk arbejde.

Vi søger en kollega med et stærkt udviklet servicegen, som vil bidrage til teamet. Dine arbejdsopgaver vil bestå af modtagelse, registrering, auditering og distribution af indkomne prøver samt afvigelsesbehandling.

Du vil blive en del af et engageret team på 5, hvor tingene ofte går stærkt, men hvor der også er tid til humor.

Junior QA Specialist søges

Motiveres du af at sikre et godt samspil mellem GMP compliance og den kommercielle drift?

Little Green Pharma er en international medicinsk cannabis virksomhed med hovedkontor i Australien. I vores topmoderne drivhuse i Odense og Perth har vi faciliteterne til at fremstille mere end 23 tons medicinsk cannabis biomasse om året, hvor størstedelen produceres i vores 21.500m2 drivhuse og vores 4.000m2 GMP godkendte produktions-lokaler i Odense, som vi har ambitioner om at vækste over de kommende år til at opnå fuld udnyttelse.

Regulatory Affairs & QA Lead

Har du lyst til at blive en del af en spændende arbejdsplads, som opererer globalt med nogle af markedets bedste produkter?

Som vores Regulatory Affairs & QA Lead bliver du en del af et velfungerende team med 5 engagerede kolleger, der hver dag arbejder målrettet og brænder for deres arbejde.

Der kan være mange indgangsvinkler til jobbet men du skal have erfaring med medicinsk udstyr, være omhyggelig, energisk og brænde for det regulatoriske arbejde.

Procesoperatør

Er du klar til at gøre en stor forskel i en dansk virksomhed med stærk global tilstedeværelse?

Du vil få ansvaret for at overvåge hele fremstillingsprocessen fra modtagelse af råvarer til fremstilling af det færdige produkt.

Dine primære opgaver som procesoperatør vil derfor være:

• overvågning og betjening af anlæggene, herunder optimering, justering, fejlfinding og prøvetagning af færdigvarer
• analyse af produkter for at sikre høj kvalitet

Trives du i et dynamisk miljø med højt tempo? Så er det muligvis dig, vi leder efter til denne spændende stilling.

Fleksibel og nysgerrig QA-koordinator med lederpotentiale

Kan du se dig selv stå i spidsen for at sikre høj kvalitet for mere end 1500 forskellige produkter årligt?

For Persano Group søger vi en QA-medarbejder, som kan se sig selv vokse ind i en ledende funktion, og som har den rette mængde af drive, nysgerrighed og ejerskab til at bidrage i en familiedrevet virksomhed, hvor stor passion er den kultur, der gennemsyrer virksomheden.

Dyrlæge med erfaring indenfor kirurgi

Vi søger en dyrlæge med erfaring inden for kirurgi til at indgå i vores kvalitetsbevidste team hos AniCura Familiedyrlægerne.

Du vil indgå i en spændende udvikling af AniCura Familiedyrlægernes faglige profil – en udvikling, du vil have mulighed for at bidrage til.

AniCura Familiedyrlægerne tilbyder en arbejdsplads med en struktureret hverdag, spændende patienter og gode muligheder for faglig udvikling og sparring med kollegaer.

Project Manager - Sustaining Engineering & PMO

We are looking for an experienced Project Manager to join our PMO, Technology and Innovation. You will lead sustaining engineering projects with multidisciplinary teams of engineers and specialists.

You will apply your project management, people leadership, and technical skills to qualify and implement changes to existing products e.g., material changes or quality updates. Together with your team you create clear ambitious plans and ensure projects are delivered on time with agreed quality, scope and cost.

Senior Product Test Engineer - Medical Devices

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.

Account Manager til måleudstyr – Pharma & biotek

Har du teknisk flair og lyst til en salgsrolle med primært fokus på pharma- og laboratoriesegmentet? Så er virksomheden klar til at uddanne og udvikle dig, så du kan skabe succes i jobbet.

Buhl & Bønsøe oplever fortsat vækst, og derfor udvider de deres salgs- og marketingteam med endnu en kollega.

Buhl & Bønsøe rådgiver om og sælger måleudstyr til en lang række forskellige brancher. I din rolle vil du have primært fokus på pharma/biotek- og laboratoriesegmentet, og i din hverdag er du opsøgende og proaktiv overfor både nuværende og potentielle kunder. I teamet hjælper man hinanden, hvorfor du også vil komme til at beskæftige dig med andre brancher.

Ruminant Nutritionist – Calf and Lamb Milk Formulations

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.

Health, Safety and Environment (HSE) Manager

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.

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