- ...andre Arbejder struktureret, selvstændigt og har en god kvalitetsforståelse Det er en fordel, hvis du har: erfaring fra GMP‑reguleret miljø kendskab til konfigurationsstyring af IT‑systemer, der skal efterleve Annex 11‑krav Har erfaring med samarbejde...
- ...for (A) technical assessment of medicinal product dossiers ('dossier assessors') and (B) audits against Good Manufacturing Practices (GMP) and Good Storage and Distribution Practices (GSDP) ('auditors'). The roster will also be used to engage experts, under UNICEF...Fjernjob
- ...LEAN ways of working, identifying improvement opportunities and bringing your team along on the journey Ensuring compliance with GMP, EHS and quality standards in everything we do Collaborating closely with six fellow Team Leaders, the Production Director and colleagues...
- ...Senior Byggeleder – Proces, GMP og Mekaniske Installationer Solvexis søger en erfaren Senior Byggeleder til et teknisk projekt på Sjælland. Vi søger en stærk site-profil med solid erfaring fra komplekse bygge- og installationsprojekter, gerne inden for pharma...
- ...Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, 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
- ...What we offer As a student Intern, you will get: Hands-on experience with training administration and coordination in a GMP manufacturing environment Close collaboration and mentoring from experienced colleagues within training and the line organisation...
- ...will include: Implementing changes to ensure continuous compliance with authority expectations, IT-security requirements, GAMP5, GMP and other regulatory standards Writing and approving change requests, test protocols and instructions to maintain system integrity...
- ...improvement. Your skills & qualifications We are looking for a skilled and quality‑conscious professional who thrives in a GMP production environment. We expect that you have: A degree in engineering (natural science related), pharmacy, or another relevant...
- ...med ansvar for op- og omstilling af sprøjtestøbemaskiner og automationsudstyr, fejlfinding, løsning samt sikring af stabil drift i et GMP-reguleret miljø. Stillingen giver mulighed for både faglig udvikling og aktiv deltagelse i forbedringsinitiativer i en...Fjernjob
- ...troubleshooting when processes do not perform as expected Handle deviations, investigations, and change requests in accordance with GMP requirements Contribute to continuous improvement initiatives and implementation of new equipment, systems, and ways of working...
- ...Senior QP Delegate (Specialist) Do you want to be part of bringing new treatments for brain diseases to patients by securing GMP‑compliant investigational medicinal products for clinical trials? This opportunity offers a broad and highly impactful quality role, supporting...
- ...Firmabeskrivelse Brænder du for arbejde med kemiske analyser efter GMP og er du klar til at blive en del af et dedikeret team? Vil du bidrage til sundhed og sikkerhed verden over ved at levere laboratorieanalyser af høj kvalitet? Så har vi den rette laborantpraktikstilling...
- ...eller bioanalytiker er et krav. Erfaring: Erfaring fra QC-laboratoriearbejde, gerne inden for medicinsk udstyr, samt erfaring med GMP er en fordel men ikke et krav. Vi søger en kollega som har erfaring med kvalificering af udstyr, metodevalideringer samt mod på at...Fjernjob
- ...identification activities (e.g. HAZID, HAZOP, LOPA), ensuring appropriate mitigation measures are defined and tracked. Regulatory & GMP Compliance: Ensure safety and risk management practices align with GMP requirements, as well as applicable HSE legislation and...
- ...: Har du praktisk erfaring i udførelse af relevante analyser f.eks. HPLC, UHPLC eller GC. Har du erfaring med at arbejde under GMP eller tilsvarende kvalitetssystemer. Er du rutineret bruger af diverse IT-systemer såsom Office, Empower og LIMS. Er du en teamplayer...
- ...Vil du stå i spidsen for kvalitetsafdelingen i en vækstorienteret GMP-virksomhed? Her får du en helt central rolle med stor indflydelse på den fremtidige organisering og udvikling af kvalitetsområdet En central rolle i en vækstorienteret virksomhed For vores...
- ...methodology in manufacturing, production, or supply chain environments; experience from pharmaceutical production or another regulated/GMP environment is an advantage. Strong practical toolbox within visual management, performance boards, daily management systems,...
- ...Vil du kickstarte din karriere i pharma-industrien og opbygge viden inden for Good Manufacturing Practice (GMP), Maintenance, Automation eller anden Ingeniør disciplin. Så har vi en spændende mulighed for dig! Vi søger en engageret studentermedhjælper til at understøtte...
- ...DESCRIPTION Work Schedule Rotational days/weekends Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Thermo Fisher Scientific fremstiller produkter, der anvendes i banebrydende forskning og i...Fjernjob
- ...erfarne kolleger, der brænder for at dele deres viden. Mulighed for faglig og personlig udvikling samt indblik i medico-branchen og GMP-regulerede processer. Arbejdsopgaver: Har du flair og interesse i at arbejde med data og konkludere ud fra disse? Kan du...
- ...del af opgaverne kræver fysisk arbejde, f.eks løft, bevægelse, opgaver både i højder og mindre rum (confined space) • Kendskab til GMP er en fordel og at du har et truckkort er et stort pluss HVAD VI TILBYDER Hos BASF får du: • Ansvar fra første dag og...
- ...suited for newly graduated candidates as well as those with prior but limited QC experience, who are motivated to learn and grow in a GMP‑regulated environment. Your new department You will join the ICP team within Analytical Development, part of Global...
- ...Supporter – 12-Month Maternity Cover Måløv Are you motivated by supporting production and ensuring high quality in a dynamic GMP environment? Join our team in Hormone Replacement Therapy production as a Process Supporter, where you will play a key role in daily...
- ...discontinuation. The role combines practical laboratory work with strong ownership of documentation, equipment, and operational standards in a GMP‑regulated setting. Your responsibilities will include: Performing laboratory production and handling of mammalian cell banks...
- ...consistent application of LOTO procedures across all work fronts. Safety & Regulatory Alignment: Ensure LOTO practices align with GMP requirements, site EHS standards, and relevant regulatory guidelines within a pharmaceutical environment. Documentation & Tracking...
- ...degree of Pharmacy and minimum +3 years of experience within QA and GDP. Furthermore, you have: Thorough experience within GDP and GMP Fluent in English Previous experience with partner and/or project management is an advantage but not a requirement Strong...
- ...Hillerød. Stillingerne er projektansættelser i længerevarende vikariater med opstart snarest muligt. Du kommer til at arbejde i et GMP-reguleret produktionsmiljø, hvor der stilles høje krav til renhed, dokumentation og præcision, og hvor arbejdet udføres efter pharma-...
- ...den nordiske organisation. Vi søger underleverandører Til Intertek i Danmark søger vi auditors (underleverandør) indenfo r GMP+, ISO 9001, ISO 14001 og ISO 45001 . Ansvarsområderne for dig som auditor omfatter audits, herunder planlægning, rapportering og opfølgning...
- ...implementation of the new electronic Quality Management System (eQMS) CANEA, together with the planning and execution of the company’s upcoming GMP certification. The position requires a strategic and hands-on quality leader with a strong regulatory mindset, solid experience...
- ...producerende organisation inden for biotekindustrien. Vi arbejder med udvikling af biofarmaceutiske produktions- og analyseprocesser samt GMP-produktion af protein-baserede lægemidler til både klinisk afprøvning og markedsføring. Laborantpraktikanter indenfor analyseområdet...
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