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- ...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...
- ...looking to further strengthen the QA Commercial & Life Cycle team located in Denmark and the United States. In this position QA GMP Senior Manager you will set the quality direction for Genmabs Commercial Supply Chain in the EU market. You will be an important part...
- ...the coming years aligned with the expansion of Genmabs commercial portfolio and global CMO network. You will be part of the global GMP QA organization and a key member of the QA leadership team reporting directly to the Team Lead of QA GMP Commercial. Key...
- ...development products. The role is a senior individual contributor position with no people or line management responsibilities. The GMP QA Senior Manager will join the global GMP QA team ensuring compliance with industry standards and regulations. This Denmark-based...
- ...måletekniske kontroller samt prøveudtagning og har lyst til at lære nyt og udvikle dig i stillingen. Det er en fordel hvis du har GMP erfaring men ikke et krav Det er en fordel hvis du har arbejdet med luftmålinger før og/eller har anden teknisk baggrund Du kan...
- ...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...
- ...Does this inspire you and feel like a fit Then we would love to have you join us! The Role Genmab is looking for a dedicated GMP Technician to join our new clinical secondary packaging and labelling facility in Ballerup which is currently under this role you...
- 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...
- ...up on audit actions where needed. You are, An experienced QA professional With 3 to 5 or more years of QA experience from GMP or ISO 13485 environments, Comfortable working independently with operational quality tasks. Pragmatic and efficient Able to...
- ...fra QC Du har erfaring med afvigelseshåndtering Du har erfaring med kundekontakt Du har erfaring med at arbejde i henhold til GMP eller ISO17025 Du taler og skriver både dansk og engelsk Personlige kompetencer kan være men ikke begrænset til: Du arbejder...
- ...automation (robots), UHPLC, and core lab infrastructure, setting direction across analytical equipment and balance compliance between GMP and GSP. You’ll coordinate closely with stakeholders across CMC to keep deliveries on track. If “unordinary drives change” resonates...
- ...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...
- ...’s degree in science within pharmacy, chemistry, or similar field. Experience working in the pharmaceutical industry and within a GMP regulated environment, are a must. Experience within the field of chemistry, manufacturing and control, quality control or similar...
- ...working with documentation of complex systems or processes A solid understanding of IT Network and data handling A strong Quality/GMP mindset with experience in technical documentation and specifications The ability to handle multiple tasks simultaneously and...
- ...mødeindkaldelser, referatskrivning og opfølgning på opgaver Understøtte kvalitetssikringsaktiviteter, herunder validering og compliance (fx GMP og ISO) Kommunikere og koordinere med interne og eksterne interessenter, herunder leverandører og kunder Assistere projektledere...
- ...noget for dig. om jobbet: Du bliver en del af pharma-produktionen, der er kendetegnet ved høje kvalitetskrav og produktion under GMP, hvilket betyder, at korrekt dokumentation og omhyggelighed er en selvfølge og en stor del af jobbet. For at lykkes i rollen er det...
- ...writing and management of quality documentation. You will also actively contribute to our efforts to achieve and maintain ISO and GMP standards, ensuring compliance with regulatory and quality requirements. Role Responsibilities As an Analytical Chemist with...
- ...advantage • Experience as Lead Auditor You are, A senior QA professional With 7 to 10 or more years of experience within QA in GMP environments and ISO 13485 environments Confident in leading discussions, influencing stakeholders and making decisions....
- ...krav til din fleksibilitet og omstillingsparathed. Derudover bliver du den drivende kraft i fabrikkens fortsatte arbejde med stigende GMP-niveau og udvikling af stadigt mere forædlede produkter. Du vil derudover blive ansvarlig for: ~Sikre en økonomisk rentabel...
- ...under tilsyn af Fødevare- og Lægemiddelstyrelsen. Produktionen er i høj grad automatiseret og afvikles efter gældende regler indenfor GMP HACCP og sikkerhed. Arbejdet foregår hovedsageligt i selvstyrende teams i et åbent og uformelt miljø. I denne rolle kommer du...
- ...AGC Biologics Code of Conduct Consistently working in compliance with regulatory and quality systems (e.g. TrackWise) Following GMP MPRs and approved procedures at all times Contributing continuous improvement ideas and actively participating in implementation...
- ...onboarding and training of new colleagues while maintaining ownership of your own learning and development Working in accordance with GMP MPRs SOPs and approved procedures at all times Ensuring compliance with quality and regulatory systems in close collaboration with...
- ...sundhedsvæsen. Du får mulighed for at præge 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...
- ...you passionate about supplier quality management (SQM) audits and inspections Are you a trained Lead Auditor with great knowledge of GMP guidelines and experience from a pharmaceutical manufacturing environment We are looking for a Senior Supplier Quality Specialist to...
- ...higher in natural sciences engineering or a related field. Minimum 4 years of experience in aseptic production. Experience with GMP aseptic filling processes and production support. Professional proficiency in Danish and English. On a personal level you are...
- ...Job Description: GMP Process Supporter 12 months position Do you have experience as a process supporter and a strong GMP problem-solving mindset Do you enjoy handling deviations driving investigations and continuously improving processes At Syntese we value...
- ...søsterafdeling på Herlev Hospital. Din hverdag Du kommer til at få en central rolle i videreudviklingen og efterlevelsen af GMP og GCP både lokalt i cytostatika produktionen og på tværs af cytostatika produktionerne i regionen. Du vil som akademiker i en...
- ...as the client’s HVAC technical authority from design through construction and handover Review and challenge HVAC designs to ensure GMP, GEP, and regulatory compliance Provide technical oversight during construction, ensuring quality, coordination, and...
- ...processing and related downstream steps, a strong track record in designing scalable processes, and solid experience working within GMP environments, supporting clinical programs, and applying modern analytical and monitoring technologies. What we offer We offer...
- ...innovative solutions Involvement in quality assurance validation and documentation processes specific to pharma. Ensure compliance with GMP and ISO 13485 standards passing internal and external audits Act as the central point of contact for internal stakeholders...