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Technical support to international sales of feed supplements

A central role at R2 Agro, combining the technical knowhow of the products with the commercial value.

Your main responsibility will be technical support to our product portfolio. This requires that you can provide technical support to our distributors and regional managers, and participate in customer meetings and technical fora.

You will have the possibility of working from home sometimes, and you will meet a lot of good, social, and skilled colleagues.

Clinical Supply Manager

The Clinical Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for all clinical trials.

You must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.

Nilpeter A/S søger en Production Planner til maskinfabrik og delmontage

Hos Nilpeter vil du få de absolut bedste kollegaer. Her går høj faglighed hånd i hånd med en uformel tone og godt humør samt frihed under ansvar.

Som finplanlægger i Nilpeters maskinfabrik vil du være ansvarlig for produktionsplanlægning i maskinfabrikken.

Nilpeter A/S udvikler og producerer avancerede trykmaskiner specieltrettet mod etiket-markedet og har produktion i Danmark, USA og Indien, samt agent- og salgsselskaber fordelt over 70 lande. Hovedkontoret er placeret i Slagelse, og Nilpeter beskæftiger ca. 450 medarbejdere på verdensplan, heraf ca. 200 i Slagelse.

Group Lead

Help us to be ready to face the energy challenges of tomorrow and make a green footprint.

We are looking for someone who:

• Ensures adherence to defined manufacturing guidelines, processes and procedures.
• Supervises production activities according to established quality standards and EHS requirements.
• Contributes to production planning processes, and determines manufacturing priorities based on established weekly production schedules.

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.

Verification Engineer

Do you want to make a difference as an engineer by contributing to maintaining the safety, reliability, and integrity of our clients’ assets throughout their life cycle. Then you should join Bureau Veritas and some of the strongest engineering professionals in the industry in this new role.

As part of our client’s safety procedures, you will verify and check findings on- and offshore, to make sure that the client is adhering to all rules and regulations always maintaining the highest safety level.

You will handle a wide variety of verification assignments from gathering logs, materials, checking structural integrity designs, lifting equipment, electrical systems including UPS etc.

Lead Auditor

Vi søger en Lead Auditor, som vil indgå i et fagligt stærkt auditteam, som har ansvaret for at udføre audit, som del af overvågning af jernbanesikkerheden i Banedanmark. Du bliver en del af Team Audit & Tilsyn, hvor du får 10 fagligt dygtige og engagerede kollegaer.

Fleksibilitet er et nøgleord hos os, hvor du kan udleve dine faglige ambitioner, uden at give afkald på work-life-balance, så udover fleksible arbejdsforhold med op til 2 hjemmearbejdsdage om ugen, får du også diverse sundhedstilbud og betalt frokostpause.

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.

Kvalitetskoordinator til indkøbsafdeling

Har du erfaring med reklamations- og kvalitetshåndtering, og vil du være med til at bidrage til optimeringen i indkøbsafdelingen?

I rollen kan du se frem til at blandt andet at skulle arbejde med følgende;

• Reklamations- og afvigelseshåndtering på indkøbte produkter
• Sikring og koordinering af årsagsafklaring, korrigerende handling og opfølgning på samme, og dette i samarbejde med relevante afdelinger og leverandører

Application Technician – Food Ingredients

We are looking for an employee with an interest in laboratory and food technology to assist in the AKV FoodLab in Aarhus, where you will become part of the team.

Here you will play an important role in relation to taking part in the ongoing laboratory work with a confident and collaborative team approach.

As an Application Technician in AKV FoodLab, your primary tasks will consist of:

• To assist the Senior Application Specialist with research by running trials of a broad range of applications in the FoodLab and conducting analysis and characterization of food products.
• Maintenance and cleaning of process equipment.
• Contribute where required in purchasing tasks for the FoodLab.

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.

Technician, EMA Solids Support Team

Welcome to Solid Support Team 13 skilled process engineers and technicians responsible for quality, introducing new products, throughput, and optimizing the products.

In this role you’ll make an impact by:

• Responsible technician for the MG-coating line, ensuring smooth and efficient coating processes for granulating with MnTACN
• Coordinate the steering system changes, bridging the gap between process engineers, technicians, and programmers to optimize operational efficiency.

Formulation Operator

As a Formulation Operator, you will operate processing equipment for the production of industrial enzymes. We’re looking for an energetic individual who is ready to tackle challenges in a fast-paced environment.

In this role you’ll make an impact by

• Operating a bridge crane, yard vehicle, and preparing raw materials for use in process equipment
• Taking production samples and analyzing those samples in the production laboratory as well as acting based on the obtained results.

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

GMP-Supporter - Danmark Protein, Videbaek

Som GMP-supporter med fokus på forbedringskultur, leder du konstant efter måder at gøre vores produktionsmiljø bedre på. Dette gælder for sikkerhed og kvalitet.

Dine opgaver vil svinge mellem at være driftsorienterede, såsom GMP-runderinger til forbedringsaktiviteter og være projektorienterede, hvor du selv driver forbedringsprojekter, støtter og udfordrer vores teams og medarbejdere på deres rejse mod en forbedringskultur.

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.