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- ...you prepared to lead the way in the dynamic field of materials for GMP production Would you like to take responsibility and drive... ...covering e.g. supplier management supply chain planning production QC QA regulatory affairs and development areas. We ensure all necessary...
- ...Er du en erfaren QA Professional Er du klar på at arbejde med kvalificeringsaktiviteter URSer og protokoller; udstyr stål og slanger... ...fokus på at sikre at ALK lever op til gældende standarder indenfor GMP! Stillingen Som QA Professional i Quality Assurance...
- ...quality assurance of Medical Device and Combination Products from a GMP and regulatory requirements perspective Are you an impactful... ...stakeholder management skills The position You will as Lead QA Professional be part of Global Quality and join a team of skilled...
- ...you and feel like a fit Then we would love to have you join us! The Role Genmab is seeking an enthusiastic and experienced GMP QA Associate Director for our brand-new Clinical Packaging & Labelling this newly established role you will set the quality direction...
- ...succeed you must hold: Minimum 2 years of experience in a relevant industry Preferable knowledge and practical experience with: GMP and ISO/FSSC 22000 Review and release processes HACCP and food safety Audits and inspections Management of deviations CAPA...
- ...GMP Coordinator CMC & Product Supply Hillerød Denmark This is a rare opportunity to shape Good Manufacturing Practice (... ...management. Collaborate with relevant stakeholders such as IT QA and AMSAT. But that is not all you will also be an essential member...
- ...prior to budget discussions and business reviews. Day to day communication and coordination with regulatory affairs supply chain QA and other stakeholders to secure plans are aligned. Support the team in communication towards external and internal stakeholders (...
- We are looking for a skilled QA Engineer to help ensure the quality, reliability, and performance of our product. You will be responsible for defining and executing a comprehensive QA strategy that supports a high standard of delivery across complex software ecosystems...
- ...Are you an enthusiastic student eager to gain hands-on experience in a laboratory setting? Join our QA lifecycle laboratory team in Pilot Plant, Mørdrup (Espergærde) and support the laboratory tasks ensuring quality and release of development of intimate healthcare...
- ...looking for a Senior Scientist. Working in the Quality Assurance (QA) for Quality Control (QC) team! You will take a leading role in... ...constantly ensure that QC and manufacturing follow current standards for GMP production i.e. EU GMP 21 CFR and ICH department fosters open...
- ...forefront of digital transformation, ensuring a competitive edge in a rapidly evolving travel landscape The Job: The Automation QA Engineer role within Kuoni Tumlare, delivering testing across various projects and individual IT developments & applications. Working...
- ...dog rings a bell you love games and if an easy-going team makes you smile this could be your dream job! We are looking for a Senior QA Tester for our silly game productions. WHAT YOU WILL DO: You will be responsible for the quality assurance of the this role...
- 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...
- ...new biopharmaceuticals to market. We are seeking a dedicated QA Scientist to join our ambitious QA for QC team in Copenhagen for... ...ensuring that all QC and manufacturing processes adhere to the latest GMP standards including EU GMP 21 CFR and ICH guidelines. We pride...
- ...forretningen og sikre, at vi til enhver tid overholder danske og europæiske krav inden for GMP og GDP. Dine primære opgaver bliver at frigive færdigvarer importeret fra andre EU-lande, lede QA-projekter og bidrage med din farmaceutiske ekspertise i komplekse problemstillinger....
- ...adherence to plans. This includes managing deviations, coordinating with QA/QC and planning and driving performance through productivity... .... Maintain a strong focus on safety and quality in a GMP and FSSC22000-regulated environment. Represent the production...
- ...opportunity We are looking for a Responsible Person (RP) to join our QA team and support the establishment of Abacus Medicine Latvia. In... ...-depth knowledge of local GDP regulations and EU GDP guidelines (GMP knowledge is an advantage) ~ Proven experience in setting up new...
- ...~ Preferably h ave experience writing reviewing and approving GMP documentation. ~ Preferably e xperience with operations of... ...interaction with Process Transfer Process Validation Engineering QA QC etc.). ~ Experience working with multiple projects...
- ...commercial supply chain subject matter experts regulatory affairs and QA teams. The LSMD team is responsible for the late-stage... ...Contract Manufacturing Organizations (CMOs) for development and GMP manufacture Manage establishment of a LCM project group within...
- ...Responsibilities: Scanning and archiving of Quality Records. QA review of Buffer Sheets. Ad-hoc tasks i.e. MPR print overview... ...Office especially Excel and Word. Prior experience in a GMP-regulated environment preferred. Working Environment: The...
- ...Responsibilities Liaison between System Users Application Managers (IT) & QA. Drives Business related aspects of system application... ...years of documented professional experience working according to GMP in a QC setting You have a thorough understanding of the...
- ...ambitiøst miljø så er du måske vores nye Senior Manager for Compliance QA (CQA). Hos CQA får du en hverdag med variation i opgaverne.... ...dit team Vi forestiller os at du har lang erfaring med GMP og tilhørende kvalitetssystemer måske fra en tidligere QA-rolle....
- ...ansvarsbevidst kollega til teamet. Derudover ser vi gerne, at du: Har erfaring med lagerarbejde eller andet fysisk arbejde Har GMP erfaring Kan læse og forstå engelsk (koncernsproget) Er hurtig til at sætte dig ind i nye opgaver. Trives med manuelt...
- ...overvågning, prøveudtagning - Dokumentation - Omstilling, indkøring etc. Din profil - Erfaring fra medinalindustrien og arbejde efter GMP regler - Gerne uddannet industri- eller procesoperatør - Teknisk forståelse Vores tilbud - Mulighed for vikariater i...
- ...design-for-installability and reliability updates. * Raise the bar on external installers: source, vet, train, certify; define SLAs, QA, safety standards; monitor performance; phase out underperformers. * De-risk delivery: identify critical path risks early; run...
- ...CTO * 1 backend developer (Laravel) * 2 full stack developers (One with DevOps) * 2 frontend developers (React) * QA Engineer * Solutions Architect We collaborate closely, review each other’s code, and take pride in building high-quality...
- ...dots between teams to make campaigns run smoothly. Like owning projects end-to-end from shaping clear briefs to hands-on execution QA and optimisation. Appreciate a dynamic environment where priorities evolve problems need solving and momentum matters. Value...
- ...similar (candidates with relevant laboratory, technical or production background, and extensive experience are welcome too) Knowledge of GMP Experience with Environmental Monitoring work in a clean utility area (water, steam, gasses) Experience in Clean room Full...
- ...onboarding and go-lives: Plan and drive the technical part of customer onboarding from kick-off to go-live, including configuration, testing, QA and handover to Customer Success. * Enable and support Customer Success & Sales: Provide hands-on training to clients and...
- ...with analytical methods from either an Analytical Development Laboratory or a QC laboratory, as well as experience from working in a GMP environment. Key personal competencies: You are a strong team player, analytical, and have a can-do attitude. Furthermore, you...