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- ...international and growing pharmaceutical company and support the Quality Assurance processes? Then here is your chance to start your career as a QA Assistant at Ascendis Pharma. Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful difference in...
- ...TFMs and Team Leaders. Provide direction and supervision to DRC HDP personnel with regards to health issues. Carry out regular QA/QC visits to the DRC HDP medical teams deployed in support of clearances activities. Ensure that the medical DRC HDP SOP Medical Support...
- ...for competence development and network building Your Skills & Talent Experience from the pharmaceutical industry working in a GMP environment You can demonstrate successful project management skills, preferably in a position as Tech Transfer Lead or CMC Project...
- ...vacuum systems for LHC Long Shutdown 3 (LS3) and the High-Luminosity LHC (HL-LHC), with a strong focus on leak detection and system QA/QC. Your main responsibilities will include: Supporting and carrying out leak detection activities and operating the insulation...
- ...Internal QA Specialist Job openings Deadline October 19, 2025 Department International Quality Assurance Join Pharmacosmos... ...As a QA Specialist, you will play a vital role in ensuring GMP compliance and quality oversight across API production, contract...
- ...temperaturövervakningssystem i frysar, kylar och produktionsområden fungerar korrekt ~ Utföra stickprov på dagliga driftsjournaler ~ Assistera QA-teamet vid Listeria- och ATP-tester ~ Vara med och ta fram utbildningsmaterial kopplat till CCP:er, OPRP:er och PRP:er...
- ...QA & Test Automation Engineer Shape the Future of Payments with Nexi in 2025 Envision a world where every transaction feels effortless, safe, and connected. At Nexi, we’re leading this transformation, building tools and solutions that redefine how the world pays...
- ...artrose (slidgigt) og ledsmerter til et bedre liv uden smerter og med frihed til en aktiv hverdag. Til hovedkontoret i Esbjerg søges nu: QA-specialist med stor erfaring inden for pharma eller fødevarer ZPD er på en transformativ rejse, hvor de forpligter sig til...
- ...In the role of Senior QA Engineer in GN’s Platform Development team , you will contribute to our purpose of Bringing People Closer. You will be part of our efforts to ensure high-quality solutions by testing, validating, and safeguarding digital products that support...
- ...for people who share our passion, drive and energy (Genki) to be part of our team in Quality Assurance - Drug Substance Manufacturing (QA DS). As part of the QA intern unit, you will deal with precisely this. Your main purpose will be to help drive a Continuous...
- ...quality processes and engaging in tech transfer projects as the QA responsible for overseeing commissioning and approving qualification... ...to our start-up phase. We prioritize high-quality standards and GMP compliance through close collaboration with our stakeholders. Our...
- ...keep up with this development. We are looking for people who share our passion, drive, and energy (Genki) to be part of our team in QA Data Team. Our Quality Data Team is dedicated to transforming the way we handle quality data across the site. Our mission is to establish...
- ...providing guidance, training, and ad hoc support to stakeholders? Then we hope you are our new colleague! Your New Role As a Senior QA for QC Specialist you will be the primary QA contact for the QC laboratory across all its activities. Your responsibilities will...
- ...documentation. Manufacturing Support consist of approx. 100 employees. In the DSM Documentation team, we provide procedural support to GMP manufacturing and ensure compliance and document release activities in a timely manner. We create and maintain the document package...
- ...Are you an experienced senior QA specialist with interest in Tech Transfer projects, quality and cross-organizational work? Then you could be our new Project QA for Tech Transfer colleague! Your New Role Our work with many different biopharma companies means that...
- ...Barselsvikar for Quality Supervisor til QA-afdelingen i Essentia Protein Solutions, Højmark Vores nuværende Quality Supervisor venter sig og derfor søger vi en barselsvikar til vores team i QA med arbejdssted i Højmark. Vikariatet varer ca. 1½ år, med opstart hurtigst...
- ...Matter Expert to join our QC Sample Control team, bringing extensive GMP experience and a talent for improvements and optimizations. If... ...of Analysis (CoA) Collaborate with stakeholders and QA to create and maintain GMP documents Initiate deviations and assist...
- ...looking for new colleagues for both our Upstream- and Downstream-QA teams Your New Role You will be pivotal in ensuring seamless... ...Knowledge ~+ 3 yrs experience in Good Documentation Practice, GMP, quality systems and legislation ~ a university degree in a scientific...
- ...quality and audit team as we are currently looking for a new dedicated QA spirited colleague! Your New Role Through your sound... ...audit experience. Preferably you have practical experience with EU GMP, cGMP and IT audits from diverse positions within the biotech/ pharmaceutical...
- ...clinical trial supply management? Do you have experience within GMP/GDP-regulated environments and managing complex clinical trial supply... ...Collaborating with internal departments (CMC, Trial Management, QA, Regulatory Affairs) Forecasting, planning, and facilitating...
- ...clinical and commercial batches. You will liaison with the operational QA DS teams, DS Manufacturing Support, Process Science and QC on... ...the batch has been manufactured and tested in accordance with GMP regulations and quality agreements. To perform QP statements in...
- ...and internal stakeholders Support maintenance of the approved GMP supplier list Support and coordinate TrackWise workflows and maintain... ...degree within life science) ~3-5 years of experience with GxP QA and supplier/auditing management, project related work ~ We are...
- ...larger team. You will be a key player in developing the features, and responsible for the quality, working closely together with QA to secure a high quality when we release new features. Profile: Collaborating effectively with cross-functional teams,...
- ...Manufacturing Organization (CDMO) serving customers in the pharmaceutical industry – from pre-clinical investigations to commercial GMP production. The Principal Database Administrator (PDBA) is the global strategic and technical lead on the design, build, management...
- ...det farmaceutiske felt og vi tilbyder den farmaceutiske industri analyser inden for mikrobiologi, kemi og proceskontrol i henhold til GMP (Good Manufacturing Practices). Stillingsbeskrivelse Vi søger en drift- og teamleder til vores mikrobiologiske afdeling. Din...
- ...growth. You'll also stay ahead of industry trends and provide a clear picture of how different tech solutions, including Google Cloud and GMP, complement each other. Project Ownership: Lead client workshops to understand business objectives, then translate those into...
- ...servicerer den farmaceutiske industri med mikrobiologiske og kemiske analyser, proceskontrol samt rådgiver om laboratorieydelser efter GMP. Mikrobiologisk laboratorium i Glostrup udfører analyser af farmaceutiske produkter for mange danske og en del udenlandske...
- ...teknisk dokumentation og evner at bringe et eksternt perspektiv til rollen. Desuden har du har erfaring med vedligeholdelsesopgaver og GMP samt netværksstruktur/konfigurering og Scada systemer. Som person er du imødekommende, serviceminded og ansvarsfuld med et...
- .... - Koordinere prosjekter, produktutvikling, leveringstid etc. - Håndtere reklamasjoner og garantisaker i henhold til rutiner og QA. - Delta i regelmessige oppfølgingssamtaler med kundene. - Arrangere og gjennomføre fysiske kundemøter ved behov. - Inngå som en...
- ...approval for shipping documents ~……..etc 3. WORKING RELATIONSHIP: ~ Internal: # ~ Sales, Trade Finance, Finance, QA, Technical 2. External: ~ Forwarders, Contract Manufacturers, Suppliers 3. Reporting: 3.1 Superior: Procurement...