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563040 DKK - 844560 DKK om året
...Fixed-term GMP QA Manager position covering maternity leave until July 2027, based in Copenhagen. Responsible for quality oversight of commercial drug products and finished goods, managing deviations, vendor compliance, and regulatory documentation within an integrated...- ...Advanced GMP Material Scientist CMC Development CMC Drug Substance Process Operations Location: Bagsværd, Denmark Your impact begins here - Turn science, data and AI into smarter GMP material decisions Are you ready to take ownership of GMP...
- ...og instrumenteringsinstallationer. har erfaring med LEAN-værktøjer og systematisk problemløsning. har kendskab til ATEX, SAP og GMP eller ISO 9000. har gode IT-kompetencer og trives med dokumentationsarbejde. kan kommunikere professionelt på dansk, både...
- ...The role involves planning and executing preventive and corrective maintenance on production equipment while ensuring compliance with GMP standards and operational quality requirements. Responsibilities Plan, coordinate, and perform preventive and corrective...
- ...Sans for kvalitet og sikkerhed i dit daglige arbejde. Nyttigt, men ikke et krav: Et gyldigt truckcertifikat. Erfaring med GMP, SAP, PAS-X eller skifteholdsarbejde. Det kommer du til at lave Du får medansvar for lagerets daglige drift og for den...
- ...muligheder for at gøre tingene bedre Bidrage til et sikkert, struktureret og velorganiseret arbejdsmiljø Arbejde i overensstemmelse med GMP samt gældende kvalitets-, hygiejne- og beklædningskrav Hvem leder vi efter? Vi søger dig, der har en stærk teknisk forståelse,...Fjernjob
- ...erfaring inden for området Kendskab til ISO 9001 og ISO 14001 Erfaring med drift og produktion fra en lignende stilling, gerne fra en GMP-reguleret virksomhed En præcis og struktureret tilgang med overblik og sans for dokumentation, kvalitetssikring og compliance...
- .../or late-phase drug substance manufacturing. Experience with scale-up and process transfer to large-scale manufacturing. Solid GMP experience from cGMP-regulated manufacturing areas, preferably for commercial processes, and a clear understanding of GMP requirements...
380 € om året
...studiejob, hvor arbejdstiden kan tilpasses til dit studie, få indsigt i kvalitetsarbejde i en virksomhed der arbejder med lægemidler (GMP-reguleret) og et godt arbejdsmiljø med mange hjælpsomme og engagerede kolleger, så send et par ord om dig selv ved at vedhæfte din...- ...stop issues reoccurring · Compliance with Hazard Analysis Critical Control Points (HACCP)/General manufacturing practices (GMP) guidelines for personal hygiene and observe security precautions as mandated by unit management. Profile Profile...
- ...synthesis or analytical characterisation LC-MS or other analytical chemistry techniques Process development or process optimisation GMP or regulated laboratory environments Why join LGC? You'll join a collaborative team at the forefront of oligonucleotide...
- ...diagnostics, biotech, or regulated manufacturing Strong understanding of manufacturing processes and operational support functions Project management and stakeholder management experience GMP-regulated environment working knowledge Fluency in Danish and English...
- ...qualification Minimum 2 years experience with injection mold maintenance and repair Fluent Danish in written and spoken form GMP knowledge and production industry background preferred Strong practical troubleshooting and problem-solving skills Ability to...
- ...Danish and able to communicate in English Experience from the medical device industry, working under Good Manufacturing Practice (GMP) requirements, or using a Laboratory Information Management System (LIMS) is an advantage, but not a requirement. Interested?...
- ...Manager, you will drive how cleaning is done across CMC Development, where our pilot plants make material for clinical trials under GMP. Acting as the functional anchor for cleaning standards, you will set direction, close compliance gaps and handle authority signals on...
- ...initiative to learn and drive innovation Experience with oligonucleotide synthesis or analytical characterization (advantageous) LC-MS or analytical chemistry techniques experience (advantageous) Process development or GMP regulated environment experience (advantageous)...
- ...and guiding quality decisions for projects Working closely with your peers, you'll help raise compliance levels, solve ad hoc GMP-related challenges, review and approve documentation for facility and equipment qualification as well as other relevant materials for...
- ...Radiometer seeks a Maintenance Excellence Owner to lead preventive and predictive maintenance strategy across multiple GMP-regulated manufacturing sites in Europe. The role drives enterprise-wide reliability initiatives, TPM implementation, regulatory compliance, and digital...
- ...DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed,...Fjernjob
- ...and compliant operation, maintenance and development of utility and ventilation systems across our Valby site. The area includes GMP-critical HVAC and clean utility systems supporting production areas, as well as a significant portfolio of ventilation and utilities...
- ...du gennemført procesoperatør-uddannelsens grundforløb? I din elevtid vil du bl.a. få erfaring med styring og overvågning af produktionsanlæg, roduktion i henhold til GMP, håndtering af råvarer, færdigvarer og kemikalier samt udfyldelse af produktionsdokumentation....
- ...flair for administrative opgaver og kan arbejde med den dokumentation, som følger med produktion under Good Manufacturing Practice (GMP) arbejder godt både selvstændigt og sammen med andre er struktureret, målrettet og forandringsparat kan arbejde på roterende...
- ...experience within pharmaceutical manufacturing, clinical supply, supply chain operations, or CMO management ~ Working knowledge of GMP and Investigational Medicinal Product (IMP) regulations, including EU and FDA requirements ~ Experience with deviation management,...
- ...and the ability to create clarity across technical and business stakeholders. Useful, but not essential: Experience from a GMP-regulated environment. Experience with project-to-operations transition, ramp-up or a new production facility. Experience with...
- ...activities for synthetic APIs, working with Contract Manufacturing Organisations (CMOs) worldwide. You will use your analytical and GMP expertise to support products from late-stage development through commercial supply. You will also help shape the processes and ways...
- ...and more, depending on your profile and existing skills. This role offers an excellent opportunity to gain hands-on experience in a GMP-compliant QC department, while developing knowledge of laboratory work, regulatory and pharmacopeial requirements, and the work life...
- ...a complex process area while working across organisational boundaries. At least 8 years of relevant professional experience in a GMP-regulated environment, including significant experience with process management, process governance or end-to-end process ownership....
- ...praktikant bliver du en del af den daglige analysedrift. Du bliver grundigt oplært i forskellige analyser og lærer at arbejde efter GMP, hvor korrekt dokumentation og sporbarhed er en vigtig del af arbejdet. Du får en fast vejleder, som følger dig gennem praktikken,...
- ...Supply Manufacturing. The role involves collecting and organizing trial documentation, performing compliance checks, and participating in GMP and GCP inspections, with opportunities to develop broader manufacturing and supply knowledge. Responsibilities Collect,...
- ...kontraktproducerende organisation inden for biotekindustrien. Vi arbejder med udvikling af biofarmaceutiske produktions- og analyseprocesser samt GMP-produktion af proteinbaserede lægemidler til både klinisk afprøvning og markedsføring. Laborantpraktikanter inden for analyseområdet...