Din browser (Safari 1.0) er mere end 3 år gammel.
Vi anbefaler at du opgraderer til den nyeste version, da vi ellers ikke kan garantere at alt funktionalitet på Jobindex vil fungere korrekt.
149 jobannoncer matcher din søgning 149 jobannoncer fundet
Vil du modtage denne slags jobannoncer på mail?
Quality Specialist
Do you want to explore your talent within the field of Quality? Does an everyday where you are the go-to-person for big and small questions regarding our internal Management System KamWay sound exciting to you?
In the role of Quality Specialist, you will have a support-oriented role, as you will act as a KamWay expert, and provide deep insight to the functionalities of our Management System KamWay, while being a valued sparring partner for your colleagues globally.
HSE Specialist
As an HSE Specialist, you will have the opportunity to develop and implement safety policies and procedures, conduct training sessions, and ensure compliance with local, state, and federal regulations.
In joining our team, you'll have the opportunity to make a significant impact, ensuring the safety and well-being of our workforce while contributing to our continued success at Duferco Danish Steel.
Auditor Specialist
We are looking for individuals who want to play an important role in supporting and performing external audits at suppliers and sub-contractors worldwide in collaboration with the Quality Manager, Lead Auditor.
You will receive an exciting and versatile job in a growing international company with a flat structure. 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.
Research & Development (R&D) Manager
As our R&D Manager, you will:
- Play a pivotal role in our Technology organization.
- Be part of a collaborative and professional R&D team, driving innovation and improvements at every level.
- Good opportunities for personal and professional development in an international corporate environment.
Embrace this opportunity to become a key player in an international company where your skills in leadership, creativity, and innovation can flourish.
Supporter til produktionsforbedringer og drift
Vil du være med til at bekæmpe kræft?
Brænder du for at lave forbedringer af processer og produktionsfaciliteter, samtidig med, at produktionen holdes kørende?
Dine opgaver vil være at stå for store og små procesforbedringer. Det kan være mindre tilretninger af SOP’er eller store forandringer som fundamentalt ændrer vores måde at arbejde på.
Vi tilbyder masser af ansvar og indflydelse på dine arbejdsopgaver.
Akademiker til daglig support og procesforbedringer
Vil du være med til at bekæmpe kræft? Brænder du for at lave forbedringer der sikrer høj kvalitet? Er du klar til at gøre en forskel for dine kolleger og forbedre produktionsfaciliteterne til gavn for Agilents kunder?
Dit hovedansvar vil være at sikre GMP-niveauet i produktionen. Du vil i den forbindelse skulle afklare GMP-spørgsmål samt udarbejde Non-Conformance Reports (NCRs).
Regulatory Affairs Specialist
We are on an exciting path of growth and are currently seeking a new specialist to join our team and play a crucial role in ensuring that our operations adhere to relevant regulations and industry standards.
A significant part of your role will be to take regulatory ownership of selected product areas, and ensure the required activities take place, to ensure we are following current regulatory standards for medical device development.
Regulatory Compliance Specialist
Do you want to influence regulatory compliance and future medical product development in a global company that provides an attractive workplace for the industry’s best and brightest?
You will play an important role in ensuring that our products meet all regulatory requirements while upholding our commitment to quality and innovation.
A significant part of your role will be to take part in planning and implementing the required documentation, including usability engineering and risk management, in compliance with current regulatory standards for medical device development.
Nyuddannet proces, - eller industrioperatør til fermentering i medicinalproduktion hos Xellia
Er du teamplayer af natur og parat til nye udfordringer?
Som operatør vil dine primære arbejds- og ansvarsområder være:
- fyldning, sterilisering, podning, fermentering og høst
- overvågning og betjening af procesanlæg
- overvågning og betjening af forsyningsanlæg, herunder vandanlæg og nedbrydningsanlæg
Kvalitetsinspektør
Som kvalitetsinspektør er dine opgaver bl.a.:
- At gennemføre inspektion af komponenter (indgangskontrol)
- 3D scanning med MetraScan Black Elite
Vi tilbyder dig muligheden for at forme morgendagens verden – uanset om du lige er startet, tager dine første karriereskridt efter eksamen eller leder efter den næste store karriereudfordring.
QA Assistant, GS-5, QAC
This position is embedded in the Quality Assurance Centre (QAC), where teams have coreresponsibilities around quality assurance and quality control of supply processes and the productswe procure and deliver.
The incumbent will beresponsible for assisting the Quality Assurance Specialist (non-pharma) in the management of all aspects of Pre-Delivery Inspection (PDI) arrangements for non-pharma items from initial request tofinal invoice certification.
Director, Supply Chain
You will play a crucial role in driving strategic initiatives and leading the transformation of our supply chain processes as we embark on a digital transformation.
This role requires a strong leader with a strategic mindset, excellent problem-solving skills, and the ability to effectively manage a diverse team.
The SCD will be responsible for procurement, quality, logistics, and operations, and work closely together with sales and the divisions, to ensure the smooth flow of materials and products across the global supply chain.
Project Manager, New Product Introduction
As a member of the New Product Introduction (NPI) team within the Production and Supply Chain (P&SC) department, you'll represent P&SC in strategic product development projects. Your responsibilities encompass overseeing manufacturing, quality control, warehouse, logistics, and sourcing & purchasing to ensure timely deliveries and high-quality outcomes.
You'll engage in the entire product lifecycle from conception to post-launch production refinement, setting ambitious goals to enhance FOSS' product development and production processes. Emphasizing a culture of collaboration and openness, you'll work closely with stakeholders across departments.
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.
Quality Coordinator
Dan-Foam er Tempur Sealys centrale produktionsenhed til det internationale marked. Virksomheden udvikler, producerer og håndterer et enestående produktprogram bestående af puder, madrasser, sengesystemer og accessories, som sælges i mere end 90 lande.
Production Engineer, 38566
Are you passionate about highly technical products and processes? Do you thrive with various task? Are you seeking a job in a dynamic work environment, and an organization in growth. Then look no further!
Your primarily responsibility will be to contribute to improving, upgrading and/or automating various production processes to achieve higher output, better quality, and reduced costs in daily operations.
Site QEHS
Brænder du for at arbejder med QEHS, kan du godt lide at arbejde i et overskueligt team – så er du måske vores nye Site QEHS på vores site i Aabenraa? Du vil være tovholder på at implementere og opretholde kvalitets- og EHS standarder.
Dine ansvarsområder bliver udvikling og implementering af QEHS-strategier, -politikker og -mål i overensstemmelse med virksomhedens overordnede mål.
Customer Success Manager for exciting robot company in rapid development
We offer an exciting opportunity to play an important role in the continued growth of TinyMobileRobots working with sports and infrastructure robots.
We improve the way our customers work and how automation technology is used in daily work, whether it's a football club marking football pitches or a larger contractor marking a major highway project.
We are looking for a service-minded customer ambassador who is patient, has a sense of humour, and an eye for detail, so our customers can always receive the best support.
Transfer Project Manager
Vil du være med til at koordinere og lede strategiske tekniske projekter, der involverer flytning af produktionsudstyr? Vil du arbejde i et miljø, hvor innovation, teknologi og bæredygtighed er i højsædet?
Det her en unik mulighed og stilling, hvor man bliver en del af et strategisk vigtigt projekt med stort fokus oppe fra. Man skal arbejde med Group Operation Strategy, Group Facility og Produktionen - så man får en bred berøringsflade og skal samarbejde med kollegaer på alle niveauer i organisationen.