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Manufacturing Lean Leader

This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

As our new Lean Leader, you will lead the site’s Kaizen funnel, daily management system, coach colleagues and work on improving for a better tomorrow. You will lead and manage projects that positively impact operations.

You will be a key staff member of the site operations team, this role exercises a high level of operational judgment, and sets team priorities in alignment with the strategic imperatives of the manufacturing site.

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.

Category Manager

Do you want to be responsible for developing our Sourcing of Packaging and Raw materials to new heights? Do you want to make a difference for patients undergoing surgery by securing the compliance of the medical devices used by healthcare professionals?

We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. 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. And we take pride in having fun.

Senior QA Specialist

You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.

We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.

Qualified Person (QP) til Danmarks største sygehusapotek

Vil du stå i spidsen for frigivelsen af Region Hovedstadens Apoteks unikke lægemiddelportefølje i en kompleks og spændende organisation?

Bredden af den medicinske produktion her på Apoteket er unikt. Hvis man gerne vil lære noget nyt hver dag, have en mission med mening, og samtidig have styr på ”balancerne”, så kom ud på apoteket.

Som QP har du det faglige produktansvar for batchfrigivelse af apotekets flere hundrede store produktsortiment, der omfatter omkring 60 registrerede lægemidler, flere hundrede magistrelle produkter, og en lang række patientspecifikke blandinger til den enkelte patient.

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.

QA Specialist

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.

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.

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.

Teknologi-entusiastisk QC-medarbejder

Vi søger lige nu en engageret og kvalificeret LIMS Udvikler i AJ Vaccines til at varetage og implementere vores nye Laboratory Information Management System (LIMS) samt sikre overholdelse af regulatoriske krav. Som LIMS Udvikler vil du komme til at spille en afgørende rolle i vores globale mission om at redde liv verden over.

Du vil være ansvarlig for at implementere og understøtte designet af vores LIMS-system ved at oprette og vedligeholde den Masterdata, der udgør rygraden af vores LIMS, og som er i overensstemmelse med vores strategiske målsætning og regulatoriske krav.

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.

Senior Engineer Device Manufacturing

Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?

Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.

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.

QA Tekniker

Vil du være en del af QA Operations Support i en virksomhed med en unik indvirkning på det globale sundhedsvæsen?

Grib denne mulighed for at blive en del af vores hurtigt voksende virksomhed, som er klar til at investere i dig. Hos os vil du ikke blot få muligheden for at påvirke produktionen af vores produkter – du får også mulighed for at udvikle dig i vores QA Operations Support Team, hvor vi ekspanderer for at kunne følge med og fortsat at kunne levere den ønskede høje kvalitet.

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.

Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.

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.

Senior QA Specialist

The Senior QA Specialist for Radiometer is responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is part of the QA Design Control department, hybrid based and located in Brønshøj. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.