Process Engineer, Enzyme Recovery, Novonesis, Kalundborg

Are you looking for new challenges in a fast-paced environment where no two days are the same?

You will be part of a team of dedicated and skilled engineers and technicians with four main responsibilities:

• Process and product responsibility including daily supervision and optimization to meet business targets for quality, economy and regulatory requirements
• Optimization activities including identifying and driving technology projects to further improve our production processes and secure future capacity

Project Manager - CAPEX projects - EMEA

The position should be based at one of our Ingredients manufacturing sites in the EMEA region. There will be flexibility for remote work.

Responsibilities/description:

• Coordinates with Project Sponsor and Divisional Engineering Director to develop Business Objectives Letter.
• Leads and provides input into developing the project objectives.

Senior Design Assurance Engineer

As a Senior Design Assurance Engineer, you will drive the subject matter expertise of our Design Control process, as well as our Risk Management process and participate in improvement of our processes, support the product documentation during all phases of NPD projects and review essential parts of the technical documentation.

Within one or more product development projects or remediation projects you will be:

• driving adherence to the design control as well as risk management processes in product development projects
• a key figure in the planning and follow-up of all design control activities.

Process & Product Specialist - Dairy

Faerch is an international business, powered by strong people. We are passionate about our products and purpose to lead the food packaging industry into true circularity.

Your primary tasks will include:

• Taking the lead in picking and defining best practices across the manufacturing sites supplying to the dairy segment
• Participating in developing and maintaining the Group Quality platform

Process Supporter - Medical devices

As a process supporter, you will be part of the production team where you will take a central role in getting Contura products released for the market. You will be interacting with a range of departments in the organization to ensure production flow.

Your strong scientific background will contribute to maintenance and update of the product and process documentation, e.g. process validations, product stability testing reports, risk analysis evaluations, design changes etc. Also, you will play an active role in completing non-conformities, corrective and preventive actions as well as change requests.

Lead Automation Engineer til Pharmadivisionen

Har du en god procesforståelse og erfaring med at arbejde i pharmabranchen, kan du måske se dig selv som Lead Automation Engineer i Pharmadivisionen.

Vi søger to nye kollegaer med en stærk automationsfaglig erfaring og kendskab til at arbejde med sterile processer. Du bliver en del af afdelingen: C&Q/Automation – en nyere afdeling som vi er godt i gang med at opbygge. På nuværende tidspunkt består den af syv dedikerede medarbejdere, der arbejder med commissioning, automation og test af anlæg. Her vil du indtage en central rolle som specialist på automationsområdet, og du vil få rig mulighed for at være med til at udvikle C&Q/Automation-afdelingen.

HSE Advisor - sundhed, sikkerhed og miljø

Har du lyst til at bidrage til den igangværende forandringsproces rettet mod at gøre sikkerhed til et hovedfokus, og fælles anliggende?

Du vil blive omdrejningspunkt for styrkelse og ændring af virksomhedens sikkerhedskultur. Dine ansvarsområder vil bl.a. blive:

• Deltage i opbygning af og vedligeholdelse af virksomhedens Arbejdsmiljø-platform (SharePoint)
• Udarbejde kampagne-materiale og pro-aktivt rådgive inden for sikkerhed og arbejdsmiljø

Senior Usability Engineer

Er du erfaren Usability Engineer og er du interesseret i at bidrage til forbedringen af brugeroplevelsen inden for høreteknologi? Og vil du arbejde i en international virksomhed, som forbedrer livskvaliteten for mennesker med hørehandicap på verdensplan?

Du kan bl.a. se frem til at sikre levering af vores høreapparatløsninger med det højeste niveau af brugbarhed til markedet. Du bliver vores ekspert i brugeroplevelser, herunder brugbarhedsmetodologi, ergonomi, adfærds- og interaktionsdesign, systemydelse og visuelt design.

Supplier Quality Engineer

Agilent provides life science, diagnostic, and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise.

Your main responsibilities will include ensuring compliance with various regulations and standards, leading supplier quality compliance projects, developing partner quality agreements, managing high visibility SCARs, and conducting key supplier audits.

Experienced engineer - Nano fabrication and optical metrology

Do you want to make a difference in a growing business working with leading edge technology and climate friendly products for a broad range of industries?

Ibsen is a global leader in design and manufacture of transmission gratings and spectrometers used by major global scientific, medical, industrial, and pharmaceutical instrument manufacturers, primarily located in North America, Europe and Asia/Pacific. You’ll be part of an organisation that has five-doubled its sales since 2014, to reach 150 MDKK in 2023, and employ 75 people at our R&D and manufacturing facility close to Copenhagen, Denmark. We have ambitious plans to grow the business further, and need your help!

Scientist Pipeline AGC Biologics

Are you passionate about ensuring quality in manufacturing processes? Do you have a scientific background and experience in Quality Assurance or Manufacturing? If so, we have an exciting opportunity for you!

You will be involved in:

• Upstream Processing: Cultivation of cells, media preparation, and bioreactor operation.
• Downstream Processing: Protein purification, filtration, and chromatography.
• Solution Preparation: Buffer preparation, media and solution mixing, and sterilization.

Manufacturing Technician Pipeline AGC Biologics

Join our production team, which consists of five production lines that manufacture preclinical, clinical, and commercial products for a diverse range of clients.

As a technician, you will be involved in planning and executing different steps in the production process, including protein purification and equipment setup.

It would be an advantage having 1+ years of experience in the biopharmaceutical or related industry, preferably in a cGMP environment.

QA-/valideringsspecialist

Eldon Biologicals A/S er førende inden for point-of-care in vitro diagnostik til blottypebestemmelse. Vi er den største producent af Dry Format Cards og vores førende EldonCards kan bestemme patientens blodtype i ABO- og RhD-systemerne på under 2 minutter.

Vi tilbyder en unik mulighed for at arbejde i en internationalt anerkendt virksomhed med fokus på kvalitet, innovation og kundetilfredshed. Vi giver vores medarbejdere mulighed for at påtage sig forskellige ansvarsområder og bidrage direkte til virksomhedens succes.

Vi glæder os til at høre fra dig!

Chemist

In this position you will be part of River Stone’s downstream processing (DSP) team, which is responsible for developing purification methods for River Stone’s biological production processes of pharmaceutical ingredients.

This includes hands-on laboratory work with bench scale volumes of product, testing out new hypotheses and optimizing existing processes.

Typical DSP work could be with filtrations (dead-end and membrane), liquid-liquid extraction, precipitation and crystallization.

Kvalitetskoordinator til udvikling af kvalitetsarbejdet

Kvalitetskoordinatorerne i Lægemiddelstyrelsen understøtter ledelsen i kvalitetsanliggender og fungerer som ambassadører for kvalitetsledelse.

Du vil inden for lægemiddelgodkendelse, kliniske forsøg og bivirkningsovervågning arbejde med vores kvalitetsledelsessystem, herunder bl.a.:

• forbedre kvalitetsdokumentationen og øge compliance, baseret på processer og dokumenter
• koordinere arbejdet og hjælpe med implementering af nye tværgående eller overordnede procedurer