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- ...du tænke dig at starte din karriere indenfor pharma-industrien og opbygge viden og erfaring indenfor Good Manufacturing Produktion (GMP), aseptik, vaccineproduktion, produktionssupport, risikovurderinger, kvalificeringer af udstyr - og samtidig arbejde med en masse skønne...
- ...erfaring med kvalitetsstyring og lyst til at præge udviklingen i en højteknologisk produktionsvirksomhed? Så er det dig vi søger som QA Manager hos Primodan A/S i Vipperød På vegne af Primodan søger Career | a JKS company en QA Manager med teknisk indsigt og sans for...
- ...outcomes. Key Responsibilities Foster a culture of accountability, collaboration, and continuous improvement within the QA team. Conduct regular team meetings, performance reviews, and skills assessments to identify training needs and career development...
NOV
4400 KalundborgIndrykket for 21 dage siden - ...you prepared to lead the way in the dynamic field of materials for GMP production? Would you like to take responsibility and drive... ....g., supplier management, supply chain planning, production, QC, QA, regulatory affairs, and development areas. We ensure all necessary...
- ...quality, compliance and continuous improvements and are you looking for an exciting development opportunity? Then you might be our new CVP GMP partner in the CVP area API Manufacturing 4 (M4). You will get a great opportunity to be part of an exciting area and the...
- ...Internal QA Specialist Driven by bold ambition and a commitment to excellence, Pharmacosmos invites you to become part of our collaborative... ...As a QA Specialist, you will play a vital role in ensuring GMP compliance and quality oversight across API production, contract...
- ...About the role DHL Supply Chain Denmark is looking for a QA (Quality Assurance) for our Inbound to Manufacturing Warehouses. We are looking for a person to ensure quality compliance at our GMP certified warehouses located outside of Allerød, Denmark. At our...
- ...quality of life worldwide, protecting our tomorrow. Join us in our mission to make a difference. We are looking for an experienced Senior QA Specialist/QP Delegate at our Kvistgaard site reporting to the site QP. You will be responsible for the release of the final product...
- ...gennem struktur, analyse og kommunikation? - Så er du måske den nye QA Specialist, vi søger til vores kvalitetsteam hos Nordic Sugar –... .... Fabrikkerne er certificeret efter IFS, ISO/FSSC 22000 og GMP+, og vi arbejder løbende på at integrere standarderne i den daglige...
- ...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...
- ...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...
- ...forskellige aspekter af audit-aktiviteter på tværs af hele virksomheden - og gerne erfaring med både interne og tredjeparts audit. Vi er en QA-funktion, der dækker alle aspekter af kvalitetssikring omkring de produkter, der produceres på sitene i Bjæverskov og Ringsted. Vi er...
- ...Vil du arbejde med høj kvalitetssikring for kunder og leverandører? Så har du nu en unik mulighed for at blive en del af QA-teamet hos Sterigenics i Espergærde – en global leder inden for e-beam-sterilisation Det får du hos Sterigenics En fast fuldtidsstilling i...
- ...både veterinær og human brug. Afdelingen arbejder tæt sammen med QA, Produktion og Registreringsafdelingen samt med eksterne samarbejdspartnere... ...af analyser og sikring af, at resultater lever op til gældende GMP-krav Udarbejdelse, opdatering og vedligeholdelse af SOP’er og...
- ...managing, and reporting stability studies in accordance with ICH Q1 and GMP requirements. You will lead a skilled team of scientists and... ...excellence. Collaborate cross-functionally with QC, QA, Regulatory Affairs, MSAT, Production, and Supply Chain to ensure...
- ...vedligeholdelses- og automationsaktiviteter er i overensstemmelse med GMP og vores kvalitetssystem Støtte og udvikle teammedlemmer... ...relationer til nøgleinteressenter som DS Produktion, Miljø, QC, QA, Global Engineering, DP og vedligeholdsteams Om dig Du er akademiker...
- ...employees across Drug Substance, Drug Product, Warehouse, QC, and QA operations. This role is pivotal in ensuring robust, compliant,... ...strategic leadership with hands-on operational engagement, ensuring GMP compliance, driving continuous improvement, and fostering a...
- ...følge op på inspektioner. Din profil Du har en baggrund som cand.scient., ingeniør eller farmaceut – og gerne erfaring med GMP, analysearbejde og den farmaceutiske industri. Vi forventer, at du: Tager ansvar for dine opgaver og følger dem til dørs. Er...
- ...procurement certification from CIPS, CPSM, CPP, NEVI or other other ~5 years plus of strategic/tactical procurement & sourcing experience, GMP (industry) experience Knowledge, Skills and Abilities: Ability to communicate effectively Excellent strategic thinker...
- ...all DP area (Wash & Sterilization, Formulation, Filling, Freeze dry, Visual inspection & Packaging) The team is responsible for the GMP on the equipment’s technical side. Become Equipment Owner in DP-Fill As our new Equipment owner, you will be second technical...
- ...systematisk problemløsning 3 og A3) Behersker dansk og engelsk i skrift og tale Erfaringer fra fødevareindustri inkl. tilhørende krav til GMP, dokumentation og compliance er en fordel Om afdelingen FGM Kalundborg omfatter 4 produktionslinjer der standardiserer flydende...
- ...high motivation to work and interface across departments in a complex and diverse stakeholder landscape. Experience working in a GMP environment supporting biopharma manufacturing operations is a plus. Work in other industrial operations environments also considered...
- ...Administration, Supply Chain Management or similar ~ UpToDate knowledge of common customs rules and regulations, and experience with GDP/GMP ~ Knowledge about Shipping Qualifications is an advantage We Hope You Are: A natural leader who thrives by being part of...
- ...applications in quality monitoring or anomaly detection. Experience working in cross-functional digitalization projects with IT, QA, and production. Why Join Us? We offer a dynamic and collaborative work environment where growth, innovative thinking and...
- ...Automation Engineer within our Plant Engineering team, you’ll play a pivotal role in shaping the future of our SCADA systems amidst a dynamic GMP environment. Bring your expertise in automation, problem-solving, and project management to our team. Together, we’ll push boundaries...
- ...Professionally, we would like you to have solid experience in the Life Science industry. As well as being comfortable working in a GMP environment and able to ensure deliveries, quality and high customer satisfaction. We expect you to have a broad knowledge of clean...
- ...til at være udstyrsansvarlig for udpeget produktionsudstyr og sikre, at det bare kører? Synes du, at det er spændende at arbejde i et GMP-reguleret miljø i rivende udvikling? Så søg jobbet som Equipment Engineer i Drug Substance! Dine opgaver Til vores dygtige...
- ...readiness and handover; coordinate release activities and run Production Performance Reviews, presenting findings and actions to NPI and QA stakeholders. Create, execute and document qualification plans for new suppliers, new materials and EOL transitions; perform...
- ...project portfolio and provide concise progress updates to stakeholders Act as the central liaison between R&D, Marketing, Retail, and QA to ensure testing supports business and launch goals Manage global tester panels and external partners to drive timely, high-...
- ...with CIP processes – including design, optimization, troubleshooting, and validation of cleaning systems. ~ A strong understanding of GMP standards and regulatory requirements related to cleaning validation and hygiene. ~ Ability to work independently and in cross-...
