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- Senior Automationsingeniør GMP Pharma, i2r/1896 Virksomheden Siden 2001 har i2r Consulting & Engineering været en troværdig samarbejdspartner primært for pharma og foodvirksomheder i Danmark. Virksomheden tilbyder at optimere og løse komplekse automations- og robotløsninger...
- ...results on projects spanning from early development to phase 3 clinical trials Ensuring all work is conducted in accordance with GMP requirements Your new department In Global Manufacturing & Supply, we cover the full value chain from drug and device development...
- ...is considered an advantage: Several years of experience within operating and maintaining plants and/or equipment. Knowledge of GMP and/or working in the pharmaceutical industry or another regulated industry. Experience with API drying processes (spray drying and...
- ...vigtig del af vores Nordic distributionscenter (NDC). Du kommer til at arbejde med modtagelse, pluk, pak og forsendelse af varer i et GMP-reguleret miljø, hvor kvalitet og præcision er i fokus. Du vil få mulighed for at arbejde med systemunderstøttet lagerstyring (SAP),...
- ...ensure that the selected system that you are focused at is integrated with other systems, instruments, process and fully in compliance to GMP requirements, continuously and systematically improving. PPV is a major project for enabling Novo Nordisk supply needed insulin...
- ...være mere i anlæg end ved skrivebordet, altså at planlægge og køre produktioner med kemikere og dokumentere og arbejde præcist efter GMP? Er du god med teknik og har sikre hænder på procesudstyr, og har du lyst til at sætte dit aftryk i Chemistry Pilot Plant? Så er du muligvis...
- ...projects that impact ventilation and air quality, where HVAC is affected by many projects requiring early involvement and advisory input GMP / quality work: Handle deviations, change cases, and structured problem-solving with the lean/engineering mindset expected in our...
- ...will be responsible for delivering best-in-class quality assurance of qualification of facilities, equipment and raw materials used for GMP production of the API for clinical studies. This includes cross functional collaboration with scientists in the API Pilot production,...
- ...area with massive strategic priority and strong attention from the top of the organisation. Are you passionate about drying processes, GMP, and the production of future medicines? Do you thrive close to operations in a high-paced environment where quality, technical...
- ...inspektionsklar til enhver tid Bidrage til teamets arbejde gennem fleksibilitet og varetagelse af ad hoc-opgaver efter behov Lære om GMP-krav, kvalitetssystemer og drift i et reguleret medicinalvirksomhedsmiljø Vi forventer at en kommende studentermedhjælper har...
- ...updated on current regulatory requirements and contribute to ensuring that operations adhere to applicable analytical standards (ISO, GMP). · Drive improvement initiatives and develop laboratory processes for more efficient and precise analysis. · Be responsible...
- ...Denmark Are you ready for a rare opportunity to take ownership of cleaning process governance and compliance in a complex clinical GMP environment? We are looking for an experienced and driven Area Process Manager, Cleaning to join CMC Development. This is a unique...
- ..., Manufacturing, and Controls (CMC) organization, where our goal is to scale-up and implement new synthetic processes as well as the GMP manufacture of novel Active Pharmaceutical Ingredients (API). The production of development candidates will be internally or using capacity...
- ...fylder fortsat mere i hverdagen. • Du får et selvstændigt job, hvor der skal tages de rigtige beslutninger i forhold til kvalitet, GMP og drift. Din baggrund: Vi forestiller os at du har erfaring fra pharma-, fødevare- eller procestekniske virksomheder, herunder...
- ...wash & sterilization process design and equipment validation activities in projects Planning and executing validation tests in a GMP-regulated environment Working closely with project offices, technical support, NPI/MPI, and other site stakeholders Applying professional...
- ...plastmager. har +5års praktisk erfaring fra et lignende produktionsmiljø. Har erfaring med produktion af medicinsk udstyr, herunder GMP og GDP. Har kendskab og erfaring med automatiske anlæg, herunder robotstyring og automatiske pakke-celler. Stærke...
- ...pharmaceutical and food industries. Our focus is on three main areas: Facility & Utility Process Equipment & Automation GMP & Compliance # As a Student Assistant, you will support various ad hoc tasks related to our company’s development in Southern Denmark...
- ...automations- og informationsløsninger samt relaterede services til denne sektor. Virksomhedens ydelser er skræddersyet til den komplekse og GMP-regulerede Life Science-industri og dækker hele produktionslivscyklussen. Målet er at hjælpe kunderne med at sikre optimal GMP-...
- ...launch. At the same time, we are handling many new and exciting customer projects and give support to processes already running in our GMP facility for clinical and commercial supply. With AGC Biologic´s increasing activities, we are looking for a new student assistant...
- ...solutions that support advanced pilot facilities. Working in high‑impact engineering projects, you will influence technical direction, GMP compliance, and project success in a collaborative environment where engineering, quality, and science come together to enable future...
- ...through commissioning and handover. You will translate production and process requirements into compliant automation solutions, ensuring GMP, quality, documentation, and testing standards are met. Working closely with customers and project teams, you will guide technical...
ABB
2750 BallerupIndrykket for 1 dage siden - ...operation of Clean Utilities and provide professional support and troubleshooting together with Skilled Workers. Own and drive critical GMP documentation for Clean Utilities, including deviations (DVs), trend reports and release documentation Provide secondary support...
- ...Compliance: Develop, execute, and review high-quality qualification protocols (IQ/OQ/PQ) and summary reports in strict alignment with GMP, GxP, and USP / ISO standards. Client Consultancy: Serve as a technical point of contact for clients, providing guidance on...
- ...projektleder med erfaring fra pharma- eller procesindustrien til tekniske projekter i Hillerød. Du får en central rolle i projekter i et GMP-reguleret pharma-miljø, hvor du arbejder med koordinering, planlægning og teknisk sparring i forbindelse med installationer i...
- ...efficient and compliant operations during production campaigns Documenting processes, flows, and system changes to ensure compliance with GMP and Good Documentation Practice This role is pivotal in maintaining flow and efficiency in a dynamic pilot-production...
- ...warehousing and distribution Experience from the pharmaceutical industry and good understanding of regulatory requirements such as GMP, GDP and FMD Key competencies: You are a strong team player, analytical, and have a can-do attitude You possess an...
- ...den nordiske organisation. Vi søger underleverandører Til Intertek i Danmark søger vi auditors (underleverandør) indenfo r GMP+, ISO 9001, ISO 14001 og ISO 45001 . Ansvarsområderne for dig som auditor omfatter audits, herunder planlægning, rapportering og opfølgning...
- ...Hillerød. Stillingerne er projektansættelser i længerevarende vikariater med opstart snarest muligt. Du kommer til at arbejde i et GMP-reguleret produktionsmiljø, hvor der stilles høje krav til renhed, dokumentation og præcision, og hvor arbejdet udføres efter pharma-...
- ...Are you passionate about clinical trial supply management? Do you have experience within GMP/GDP-regulated environments and managing complex clinical trial supply chains? If so, now is your chance to join Ascendis Pharma as our new Clinical Trial Supply Manager. Ascendis...
- ...internal and external audits and regulatory inspections. Overseeing in-process and final inspections, product release, and adherence to GMP standards. Investigating and documenting nonconformances, performing root cause analysis, and recommending dispositions....
