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Aftersales Technical Project Manager

Hovedopgaven i jobbet vil være at lede og gennemføre de projektopgaver, der er i forbindelse med, at der skal udvikles en levetidsforlængende løsning som kan tilbydes i markedet.

Sammen med de øvrige kolleger i Aftersales vil du få en væsentlig rolle i at sikre, at de projekter der er omkring dannelse af refurbishment-produkter samt projekter omkring vedligeholdelse og upgrades bliver gennemført korrekt inden for tid, anvendelse af ressourcer og det aftalte omfang.

Project Manager – projects with direct customer dialogue

Do you first and foremost see project management as your profession?

Are you at the same time looking for an opportunity to utilize your experience to impact the overall direction for the future while at the same time working hands-on with exciting customers and projects? If so, this job is tailored to you.

Your focus will be projects centered on electrification/automation/control systems across Danish industry, energy and utility companies.

Process Engineer

The Process Engineer will be responsible for process engineering and technical support of Tetra Pak capital projects, as well as specification of equipment and functional design within the given time and budgets.

You should be prepared to travel approximately 30% of your time to meet colleagues, customers and suppliers to fulfil the role (internationally, with extensive travel throughout North Europe & Benelux).

Industrial Engineer

Want to work in an innovative setting and eager to put your technical knowledge to good use?

You will work within the aluminium production area at our factory in Østbirk. Here, you will be instrumental in the development and upkeep of our production tools through the introduction and implementation of new technology and manufacturing processes.

Test & Reliability Engineer - Sustaining Engineering, Medical Devices

Do you have a keen eye for Physical Testing, Product Quality, Reliability, Validation, and Documentation? Are you looking for an opportunity to merge your passion with our expertise in the Test and Verification of Infusion Care Medical Devices, for the treatment of chronic diseases such as Diabetes and Parkinson’s Disease?

As a Test Engineer, you will be involved in developing and working with a diversity of physical test methods. Planning and coordinating tests in our laboratory in Osted near Roskilde, and partners within Global Convatec and external. Most of your time, you will be part of a project team in SEG.

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.

Project Delivery Manager – Customer Sales & Support Centre

Er du kundeorienteret og har erfaring med projektledelse? Kunne du tænke dig at udnytte dine tekniske kompetencer og viden indenfor pumper og fjernvarme?

Dit primære ansvar bliver at understøtte vores interne og eksterne kunder med at lede projekter i alle faser fra salg til levering. Du repræsenterer Grundfos mod kunden og udvikler og vedligeholder relationer til kunder og samarbejdspartnere.

Data-Driven Production Test Engineer with Coordination Skills

Do you have experience with data management, production data analysis and databases?

You will administer the operation of the WATS database (our main production database) and auxiliary data systems for test reporting. You will be constantly in contact with the team and suppliers to identify data chain gaps & potential improvements. Correspondingly, you are able to map WATS features to our organizational needs and potential improvements.

Site Manager

Er du vores nye jonglør?

På kundens site har vi behov for en Site Manager, der forstår at styre processen det sidste og vigtige stykke af vejen. Du vil derfor fungere som leder af hele siteteamet og have det fulde ansvar for installationen, herunder interne og eksterne leverancer.

Installation og implementering er en kompleks proces, der kræver gode kommunikationsevner og evnen til at håndtere f.eks. justeringer af projektet på stedet, ligesom der er behov for en forståelse for detaljerne, der sikrer, at sådanne justeringer bliver dokumenteret.

Project Manager – Test & Verification

You get the possibility to be a key person in Foss New Product Development projects by ensuring high quality and product compliance to our world class analytical solutions.

As a member of the R&D Hardware Test & Verification team, you will be one of three Project Managers responsible for overseeing all reliability, environmental, and legal testing of instruments used in analytical solutions. Additionally, you will plan and ensure that our team develops and integrates value-adding production tests, which are crucial for the seamless assembly of the instruments.

Biocompatibility Specialist

We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.

This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.

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.

Quality Supervisor til Maintenance Execution

I denne rolle vil du udvikle og implementere kvalitet i planlægning og udførelse af vedligehold, og lave kvalitetskontrol af det udførte vedligehold og dokumentation.

I revisionsperioder vil du agere supervisor på lige fod med afdelingens maintenance supervisorer for de eksterne leverandører på Avedøreværket, H.C. Ørstedværket og Svanemølleværket. Du vil arbejde ambitiøst med kommunikation og dialog med mange interessenter.

Creative Assistant

Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?

Your Focus will be:

• Always following correct compounding procedures
• Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
• Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.

Validation Engineer

As our new Validation Engineer, you will be responsible for validation and qualification of processes and equipment related to customer projects.

Key responsibilities in this role include, but are not limited to:

• Validation and Qualification of processes and equipment when implementing new material.
• Perform Validation and ensure results are accurately documented.

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.

Quality Specialist

We offer flexibility, a high degree of freedom under responsibility and you get ample opportunity for personal and professional development as part of a professional team with an informal tone.

We build a green future together with someone who can:

• Be responsible for continuous quality improvements in projects and in operational processes
• Participate in our continuous efforts improving our Document- and Project Management System
• Facilitate a high-quality culture within projects by close collaboration with QC team

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.

Specialist in Organic Coating Processes and Chemicals, Materials & Processes Engineering Department, Terma Aerostructures A/S.

Your role involves overseeing all organic coating processes, ensuring compliance and quality of materials such as epoxy- and polyurethane-based paints. You will also manage the requirements for consumable chemicals, like solvents for surface cleaning.

The responsibility furthermore entails the overall responsibility for REACH surveillance and chemical substitution activities at our Grenå manufacturing site, in close collaboration with other process owners.

QEHS Manager

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

Do you want to help develop the protein of the future, which will make it possible to feed the world's growing population without damaging our ecosystems?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.