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- ...central rolle i driften og udviklingen af steril lægemiddelproduktion – og være medaktør i en større fabrikstransformation med fokus på GMP, LEAN og robust drift? Så læs videre her. Region Hovedstadens Apotek søger 2 erfarne GMP supportere til Drift Support teamet i...
- ...er selvstændig og initiativrig, og du kan tage ansvar og sætte standarden for Health, Safety, Quality, Environment og Compliance og GMP+/ISO arbejdet på tværs af vores operationer. Stillingen er nyoprettet, og du får derfor en unik mulighed for at opbygge, strukturere...
- 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...
- ...proficiency in English (spoken and written) It’s an advantage if you have experience from the pharmaceutical industry/knowledge of GMP and experience with cLEAN® . About the Department In Product Supply (PS) API in Kalundborg, we manufacture the high quality...
- ...søger en laborant til vores laboratorium i Lystrup tæt ved Aarhus, hvor du vil blive tilknyttet vores syntese-afdeling med fokus på GMP-produktion. Stillingen er en fuldtidsstilling på 37 timer ugentligt med opstart hurtigst muligt. Velkommen til LGC Biosearch Technologies...
- ...en del af opgaverne kræver fysisk arbejde, f.eks løft, bevægelse, opgaver både i højder og mindre rum (confined space) Kendskab til GMP er en fordel og at du har et truckkort er et stort pluss HVAD VI TILBYDER Hos BASF får du: Ansvar fra første dag og mulighed...
- ...ensuring that warehouse facilities, utilities and validated solutions are designed, operated and expanded in a way that supports both GMP requirements and efficient, sustainable daily operations. While inspection readiness is an important part of the role, your main...
- ...technical background in HVAC systems or ventilation to participate in both operations, support, and projects in connection with our GMP production supplying products for patients. ~2-3 years of GMP experience or more ~ You have a good technical understanding and...
- ...Research Scientist Måløv, Danmark, Onsite CMC Development Do you thrive in a dynamic GMP-regulated environment, managing diverse tasks across multiple projects under tight deadlines? Are you passionate about taking ownership of processes, equipment qualification...
- ...på vores API Produktionssite i Lumsås. Din nye rolle Du vil være med til at sikre, at analyserne opfylder myndighedernes GMP-krav, så vi leverer produkter, der giver patienterne en sikker og god behandling. Vi har ansvaret for bla råvarer, der indgår i den kemiske...
- ...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...
- ...procesoperatør, industrioperatør eller en håndværksmæssig baggrund inden for fødevareindustrien •Tidligere har arbejdet med fødevareproduktion, GMP eller lægemidler er du interesseret? Tryk på knappen ”Ansøg” for at sende dit CV. Når stillingerne er besat, bliver...
- ...Pilots - Purification Pilot Plants Brænder du for tørring og produktion af kommende lægemidler? Trives du med at arbejde under GMP i et miljø, hvor tempoet er højt og ingen dage er ens? Vil du være en del af et stærkt, fagligt fællesskab, hvor nysgerrighed, samarbejde...
- ...stability, quality and continuous improvement on the shopfloor while supporting an expanding production area. Join a team where your GMP knowledge and problem‑solving skills truly matter. Your new role In this role, you will play a key part in ensuring stable,...
- ...dokumentation af vores arbejde. Det bliver også din opgave at sørge for, at produkterne lever op til kvalitets- og myndighedskrav herunder GMP, som er en forudsætning for vores produktion. Der køres 3 holdsskift, både hverdag og weekend. Da vi endnu ikke er i...
- ...Analysis in Emerging Technologies (ET). Your new role As a Senior Analytical Scientist - API, you'll provide scientific and GMP expertise to CMOs globally, ensuring robust analytical programs are implemented and maintained throughout product life-cycles. Working...
- ...projects Handling operational issues and supporting the sites in minor and major deviations Drive minor projects yourself Ensuring GMP documentation after re-qualifications Managing master data for our ventilation equipment In CMC API Pilots there is a strong...
- ...in Hillerød, you will be the Senior SAP Supporter who builds a reliable SAP PM/MM foundation for maintenance and calibration in a new GMP production facility. That is: Setting standards, structuring equipment and spare parts data, and ensuring processes run smoothly in...
- ...stilling giver dig mulighed for at blive en del af en førende medicinalproduktion, hvor du skal bidrage til opretholdelsen af et højt GMP niveau til vores warehouses, samt sikre løbende optimering af vores processer. Som Intern får du en varieret dagligdag. Du vil blive...
- ...Significant hands-on experience with industrial machinery and technical problem solving Experience working in a regulated environment (GxP/GMP pharma is ideal; other regulated industries can also be relevant) Strong understanding of qualification/validation and working in...
- ...Portal, Sattline, Procos or similar). Understanding of Windows OS, network structures, AD setup, and perhaps experience working in GMP environments. Fluent in Danish (written and spoken) and proficient in English. A collaborative, proactive, and solution‑...
- ...regulatory requirements, maintaining the validated state of all RC systems and keeping documentation current and Good Manufacturing Practice (GMP) compliant Monitoring and optimising system performance through data analysis, implementing energy-saving initiatives and...
- ...relation to environmental monitoring in the pharmaceutical or other highly regulated industry. Knowledge of Good Manufacturing Practice (GMP), aseptic production and microbiology. The ability to confidently present to authorities in audits and inspections. Full...
- ...Senior IT Manager CMC & Product Supply Kalundborg, Denmark Lead IT operations at the heart of a highly complex, GMP-regulated production environment – while still playing a key role in enabling major engineering projects. This is your opportunity to drive...
- ...curious about how other teams and departments operate, both inside and outside of Novo Nordisk Handling deviations in accordance with GMP requirements We are on a journey of digitalizing our QC laboratories by introducing automated processes and connecting...
- ...production equipment ~ Experience working in production settings with knowledge of quality processes, pharmaceutical processes and GMP requirements ~ Strong analytical and communication skills, with the ability to collaborate across cultures and organisational levels...
- ...leading or supporting our investment projects that enhance aseptic production capabilities while adhering to Good Manufacturing Practice (GMP) standards, we encourage you to apply today! The Position: As a Project Manager, Aseptic Production Projects – 15-month...
- ...project management Show experience with late phase (phase 3 and ongoing) pharmaceutical development projects Apply knowledge of GMP, ICH guidelines and regulatory requirements to ensure compliance Leverage experience with method validation and analysis of...
- ...Practical experience with UHPLC, HPLC, GC, NMR or other relevant analytical techniques. Preferable practical experience working under GMP or similar quality systems and capable to work in a structured way. Ambitious with a positive mindset and happy to work both...
- ...Experience in pharmaceutical development, manufacturing, or technology transfer, preferably within the biologics Strong understanding of GMP requirements and pharmaceutical quality systems Excellent collaboration skills and communication skills and are an individual who...