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Head of Business Process Optimization

Do you excel at improving business processes and leading employees in the right strategic direction?

As Head of Business Process Optimization, you will be responsible for building and maintaining our capability to develop, implement, and continuously improve business processes.

Senior Research Technician

Do you want to use your experience and problem-solving skills to work with pharmaceutical product development and early-stage development with a focus on characterization (MFI, DSC, HPLC)?

As a senior research technician, you will spend most of your time in the lab, where your primary role will be to prepare, plan, and perform pharmaceutical development work, including stability studies.

EHS Specialist

Er du fyldt med energi og passion for Health and Safety? Vil du være med til at sætte dit præg på vores sikkerhedskultur og arbejde mod en fremtid uden arbejdsrelaterede ulykker og sygdomme?

Bliv en del af vores dedikerede hold, og vær med til at forme en stærk sikkerhedskultur, hvor systemerne ikke blot forstås men også implementeres på alle niveauer. Din hverdag vil være alsidig og udfordrende, hvor du vil understøtte arbejdsmiljøorganisationen, analysere hændelser, træne kolleger og eksterne håndværkere og udvikle effektive procedurer.

Column Pack Operator

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us. We’re growing our locations, our capabilities, our teams and looking for passionate, mission-driven people who want to make a real difference in people’s lives.

We are currently looking for candidates to work within Drug Substance Manufacturing (DSM) Support and become part of a newly established team, responsible for preparation, packing and qualification of chromatography columns.

Drug Substance CIP Process Supporter

Are you passionate about pharmaceutical CIP? Do you know processes and optimizing production?

As a CIP Process Supporter (Cleaning In Place), you will have a cross-functional role as a link between production, support teams, and technical support.

Your primary focus will involve optimizing our vaccine production and ensuring robust operation in line with CIP requirements and regulations. Additionally, you will play a vital role in daily troubleshooting, collaborating across diverse professional groups to ensure a streamlined production process.

QA Assistant

Motiveres du af en stilling, hvor du har fokus på systemer og kvalitet? Og vil du arbejde med fremstilling af pakkematerialer til den farmaceutiske industri?

Du vil få daglig sparring med operatører, specialister og ingeniører i vores produktionsenhed i Horsens – som årligt producerer ca. 2,5 milliarder enheder.

Vi tilbyder en spændende stilling med mulighed for at sætte dit personlige præg på måden, tingene fremadrettet skal gøres på.

QA-specialist, der er QP-delegeret eller drømmer om at blive det

Drømmer du om at bidrage til at sikre kvaliteten af livsvigtige lægemidler, der redder liv? Er du en erfaren kvalitetsspecialist med erfaring fra lægemiddelproduktion?

Som delegeret Qualified Person (QPd) i vores Manufacturing QA (MQA) afdeling får du en unik mulighed for at arbejde med kvalitetssikring og frigivelse af Xellias produkter. Du vil være med til at sikre, at vores antibiotika når frem til patienter i hele verden i den højeste kvalitet. Som delegeret QP hos Xellia får du et stort ansvar.

Regulatory Affairs Clinical Specialist

Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.

Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.

Laboratory Technician

Til vores QC laboratorium søger vi en engageret og dygtig kollega til et 1-årigt vikariat i et af vores teams.

Dine daglige arbejdsopgaver vil bl.a. bestå af

• Udførelse af kvalitetsanalyser f.eks. viskositetsmåling, autotitrering, pH-måling, filtrering og tørstofbestemmelse
• Udførelse af applikationsanalyser i driftslaboratoriet
• Kalibrering af relevant udstyr i henhold til kvalitetssikringsinstruktioner

Arbejdsmiljøet er friskt, behageligt og til tider travlt, men med spændende udfordringer og indflydelse på egen hverdag. Vi har en uformel omgangstone og rummelige kolleger, hvor humor er en vigtig del af hverdagen.

Manufacturing Associate - Operator

We are looking for process operators, preferably with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their Bachelor or Master degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.

We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools.

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.

Procesingeniør

Har du lyst til at starte din karriere med at arbejde inden for farmaceutisk produktion? Og har du mod på at bevæge dig ud i tværfaglige udfordringer, der ligger lidt uden for din uddannelse?

Vi er en virksomhed i vækst, og produktionsvolumenerne vokser – så derfor har vi et stort behov for at styrke vores ingeniørgruppe med et nyt medlem, der kan medvirke til, at vi får moderniseret vores udstyr, som produktionen vil få stor gavn af.

QC-laborant med varierende opgaver

Har du lyst til at sikre kvaliteten af vores API’er i en QC-funktion, hvor du får lov at løse en palet af forskellige opgaver? Har du lyst til at blive en del af en velfungerende gruppe, hvor du løbende bliver trænet i nye opgaver af dine erfarne kolleger?

Så er det måske dig, der er vores kommende QC-laborant. Vi er i en proces, hvor vi vokser, og derfor søger vi en laborant, der trives med fleksibilitet og gerne vil udvikle sig.

Vi vil altid være lydhøre over for den enkelte laborant. Hvis du har interesse for en opgave, så lytter vi og sørger for, at du bliver trænet i den og får lov til at løse den

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

QA Engineer – ensure the quality of our software solutions for pharmaceutical drugs and devices

Do you want to play a key role in delivering software systems that are compliant to the pharmaceutical industry?

As Quality Engineer, you will work together with the project manager, the software developers and the customers validation teams and help secure that our solutions are compliant and lives up to the customers expectation so they can re-use our validation as their own.

You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.

Vision Engineer – ensure the quality of pharmaceutical drugs and devices

Do you want to play a key role in delivering vision inspection solutions for advanced production machines?

As Vision Engineer, you will implement inspection solutions that improve patient safety by ensuring the quality of pharmaceutical products and devices.

You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.

Erfaren akademiker til procesforbedringer

Vil du være med til at bekæmpe kræft? Brænder du for at lave forbedringer? Er du klar til at gøre en forskel for dine kolleger og forbedre produktionsfaciliteterne til gavn for Agilents kunder?

Stillingen er i Filling And Packaging (FAP), der er en del af produktionen i Agilent, Glostrup. FAP har to producerende afdelinger (Filling og Packaging) med i alt 25 operatører og et supportteam på 7 produktionssupportere. Vi fokuserer på at levere diagnostiske produkter af høj kvalitet til vores kunder. Du bliver en del af vores team af produktionssupportere, der skal understøtte og optimere produktionen i Filling og Packaging.

Quality Assurance Specialist

Would you like to be part of a strong and very skilled QA team supporting the qualification of GxP manufacturing equipment, facilities and utility systems?

You will be part of a well-founded team with 8 colleagues (4 Equipment qualification + 4 Environment) for Equipment qualification in QA Operations reporting to the QA Ops Manager for Qualification and Environment.

Facility & Utility Engineer med fokus på løbende forbedringer

Brænder du for at sikre den daglige drift og vedligeholdelse inden for facility & utility? Trives du med at koordinere og dagligt være i kontakt med eksterne håndværkere? Kan du lide at planlægge, koordinere og strukturere vedligehold af tekniske installationer og bygninger?

Til denne spændende stilling vil du indgå i en PMO og Utility/Facility afdeling, hvor opgaverne er mange og alsidige. Du vil få den daglige sparring med ingeniører og teknikere i produktionsenheden i Horsens. Du vil varetage en lang række opgaver inden for optimeringsprojekter, og sikre at Facility og Utillity installationerne til stadighed opfylder kravene.