- ...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...
- ...practices for clinical regulatory operations, ensuring efficient cross-functional workflows, documentation control, and compliance with GCP/GMP/ICH guidelines. Monitor evolving regulatory guidelines in clinical development (U.S. FDA, EMA, other major regions), identify...
- ...Are you driven by operational excellence and a strong interest in GMP equipment qualification and validation in a high-impact life science setting? Do you excel at generating and reviewing qualification documents to a high standard, ensuring compliance and facility inspection...
- ...Does this inspire you and feel like a fit Then we would love to have you join us! The Role & Department Genmab is seeking a GMP QA Senior Manager forLate-StageDevelopment QA in Denmark to set quality standards for our development GMP QA Senior Manager will join...
- ...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...
- ...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...
- 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...
- ...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...
- ...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...
- ...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...
- ...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...
- ...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...
- ..., recruit, and train the Quality team while ensuring adherence to company procedures. • Implement effective policies for hygiene, GMP, and HACCP tailored to the business. • Foster a strong food safety and quality culture across all levels of the organization. •...
- ...for Life Science - proces- anlægs- og hygiejnedesign instrumentering industriel automation industriel IT og validering i henhold til GMP og GAMP. Sammen med vores kunder konstruerer vi effektive sikre og miljøvenlige produktionsanlæg inden for pharma og bioteknologi....
- ...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...
- ...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...
- ...studying? Are you interested in working in a pharmaceutical Contract Development and Manufacturing organization and gain experience within GMP? Do you have an interest in supply chain and logistics? Then you should consider this student job in Logistics. As a student...
- ...IT/OT Infrastructure Specialist you are the guardian of our production backbone ensuring our OT infrastructure runs flawlessly in a GMP-regulated environment where every second counts. Your work directly safeguards product quality data integrity and uninterrupted production...
- ...would love to have you join us! The Role Genmab is expanding its QA for QC team and is seeking a senior QA for QC Specialist GMP QA hired at Associate Director level to support the GMP QC laboratory in Ballerup. The role is a senior individual contributor...
- ...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...
- ...Job Description: Operational Technology (OT) Specialist Do you have strong technical knowledge and a GMP mindset Do you enjoy troubleshooting at application and logic level identifying root causes directly in automation code and process execution logic At...
- ...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...
- ...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...
- ...and regulatory requirements Having chemical knowledge and responsibility Driving the scientific work to ensure compliance with GMP standards High quality systematic problem solving of production problems and continued improvements Optimization activities by...
- ...3D fit tolerances welding surface roughness etc. Your background also includes driving standardization and you are familiar with GMP GEP CE and ATEX requirements. Who you are You are a results-driven high-energy professional who maintains focus and a positive...
- ...Danfoss VLT ~ Industrielle Netværk ~60-364 samt 60-204 standard og normer ~ Læsning og forståelse af nøgleskemaer ~ Arbejde i GMP-miljø ~ DALI lyssystem Det er endvidere en forventning at du kan begå dig i forhold til Ms Office pakken og kan udtrykke dig...
- ...with an appetite for analytical methods Excellent collaboration and communication skills in English Experience in pharma or GMP environments is an advantage. Personal Skills We are looking for someone who is: Open honest and positive in communication...
- ...Assistant in our QC Department you will be responsible for managing multiple tasks related to supporting our QC teams scanning and archiving GMP documents freezer inventory and other ad hoc tasks. Furthermore you will get great insight into the biopharmaceutical industry. The...
Gmp job Danmark
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