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- ...GMP Packaging Specialist, Finished Goods Production Are you passionate about creating an environment where quality, compliance, and production efficiency go hand in hand? Do you have a solid understanding of GMP requirements and experience in Finished Goods Production...
- ...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...
- ...Har du lyst til at kombinere teori med praksis og få indsigt i, hvordan kvalitet, GMP/GDP og logistik spiller sammen i en højt reguleret medicinalvirksomhed? Så har vi en spændende stilling som studentermedhjælper hos Specific Pharma, der er den førende leverandør af ikke...
- ...procesoperatør, industrioperatør eller en håndværksmæssig baggrund inden for fødevareindustrien •Tidligere har arbejdet med fødevareproduktion, GMP eller lægemidler er du interesseret? Tryk på knappen ”Ansøg” for at sende dit CV. Når stillingerne er besat, bliver...
- ...vedligehold af to produktionsfaciliteter, herunder produktionsudstyr samt forsynings- og ventilationsanlæg. Vi arbejder i et reguleret GMP miljø, hvor stabil drift, korrekt vedligeholdelse og valideret udstyr er fundamentet for vores succes. Samarbejde, videndeling og...
- ...key role in ensuring stable, compliant and efficient warehouse operations supporting tablet production. This is a hands‑on role where GMP knowledge, structure and collaboration make a real difference. Your new role As Process Supporter, you will support and...
- ...in-house capability, bring valuable input to the implementation of SAP ERP procurement system, and qualify the vendors who meet our GMP standards. You will work closely with Manufacturing, Quality, Supply Chain, Process Development, Facilities, and Finance to keep clinical...
- ...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...
- ...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...
- ...internship, project work, thesis, or early professional experience) Interest and/or experience working in a regulated environment (GxP/GMP pharma is ideal; other regulated industries can also be relevant) Basic understanding of qualification/validation and working in...
- ...Produktionen foregår i både klassificerede og ikke‑klassificerede områder, og arbejdet sker i henhold til bekendtgørelse 507 samt dele af GMP. Dine primære arbejdsopgaver I support vil din arbejdstid være delt mellem driftsopgaver og projekter. Driften består bl.a....
- ...gained through practical experience Bring strong expertise within PV, including solid knowledge of international PV legislation, GVP, GMP and GCP Have solid experience with handling contracts, especially experience with PV agreements would be highly beneficial Are...
- ...and troubleshooting Familiarity with industrial networks and communication protocols such as OPC‑UA and Profinet Knowledge of GMP / GAMP requirements in pharmaceutical or other regulated industries To apply for this opportunity please email ****@*****.***...
- ...supported, and able to do their best work. Flat by design. We work across teams rather than in silos. Whether you’re collaborating with GMP production, academic partners, or leadership, your perspective matters. We prioritise partnership over hierarchy. Backed, but...
- ...aseptic filling processes Performing risk assessments and contributing to process design decisions Developing and maintaining GMP documentation, including GMBRs in SAP/PAS-X Collaborating with project stakeholders to ensure operational readiness of the new line...
- ...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...
- ...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...
- ...and digital manufacturing. You will implement robust process controls, centerlining, and proactive performance monitoring to sustain GMP compliance, while working to standardize core processes across sites to enable efficient replication and scale‑up. You will contribute...
- ...updated on current regulatory requirements and contribute to ensuring that operations adhere to applicable analytical standards (ISO, GMP). · Drive improvement initiatives and develop laboratory processes for more efficient and precise analysis. · Be responsible...
- ...Solvents Department. Working closely with your colleagues, you will support daily operations and contribute to continuous improvements in a GMP-regulated environment. Your key responsibilities will include: Monitoring and analysing cleaning data, handling deviations and...
- ...med varierende og udfordrende opgaver indenfor drift, vedligehold og optimering af højteknologiske, fuldautomatiske pakkelinjer i en GMP-reguleret produktion. Som vores nye procestekniker vil du blive en del af et team, som arbejder med at opretholde vores høje leveringsevne...
- ...at skabe struktur i komplekse driftsmiljøer? Så er det måske dig, vi leder efter. Lederrolle med ansvar for kontorrengøring og GMP rengøring Vi tilbyder et job, hvor du får ansvar for at lede, motivere og supportere dine medarbejdere, så I sammen kan sikre en...
- ...stakeholders (rather than a traditional salesperson) Understanding of automation or related technical disciplines Knowledge of GMP requirements, including documentation and compliance processes, is an advantage Motivated and comfortable working in a customer-focused...
ABB
2750 BallerupIndrykket for 21 dage siden - ...strong, hands ‑ on expertise in pharmacovigilance. You bring extensive knowledge of international PV legislation, including GVP, GMP, and GCP, and have experience across multiple PV roles. You have a proven track record of providing robust PV guidance in diverse...
- ...and digital manufacturing initiatives. Key Responsibilities Design, configure, and support Werum PAS-X MES solutions within GMP manufacturing environments Develop and maintain PAS-X Core 3 functionalities including: Master Batch Records (MBRs)...
- ...projektledelse. Dine fire primære ansvarsområder 1) Compliance & Kvalitet i Life Science Overordnet ansvar for compliance i GMP-regulerede miljøer Ledelse af et specialist team med ansvar for planlægning og fire GxP-koordinatorer og kvalitetsansvarlig...
- ...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...
- ...based on standard project concepts and architectures. Prepare complete and compliant project documentation and ensure alignment with GMP, quality, and contractual requirements. Participate actively in testing, installation, commissioning, and handover activities....
ABB
2750 BallerupIndrykket for 14 dage siden - ...er måske uddannet industrielektriker, automatiktekniker, VVS montør, smed eller lignende. Erfaring fra fødevarebranchen eller andre GMP-regulerede miljøer vil være en stor fordel. vi forestiller os, at du: • Er ekstremt selvstændig og trives med at træffe beslutninger...
- ...strong interest in developing understanding) of CMC regulatory requirements and guidelines (e.g., FDA, EMA, ICH) and experience with GMP and CMC-related documentation Structured and methodical approach to work, with familiarity in project management tools Strong written...
