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- ...training for new HMA teams in NTS, EOD, MMC and BAC. Deploy HMA teams effectively and efficiently. Manage and quality assure (QA) HMA activities. Ensure projects are implemented on donor targets, and up to expected quality. Continuously assess prevailing security...
- ...fairs for competence development and network building Skills & Knowledge Experience from the pharmaceutical industry working in a GMP environment, incl. experience with pharmaceutical manufacturing equipment. Solid understanding of drug product manufacturing and/...
- ...skills • Hands-on, curious, and eager to learn. • Team player, independent, articulate, and proactive in a fast-paced environment. QA knowledge (manual/automation testing) is a plus Knowledge of CRM technology or other Software is an advantage. We offer YOU...
- ...position The position is designed for students who have a keen interest and passion for enhancing daily operations and ensuring correct GMP and documentation. The primary responsibility is to assist the teams in their daily activities. Key tasks may include: Update/...
- ...extensive support to the Mission Classification activities. The overall PA discipline will include: becoming familiar with PA/QA practices, methodologies and disciplines (PA/QA, RAMS (reliability, availability, maintainability and safety), software PA, EEE components...
- .... The position We offer an exciting opportunity to obtain valuable insights and learnings within Good Manufacturing Practices (GMP), critical activities and the future manufacturing processes. This is a challenging 1 year fast-track learning journey where you will...
- ...goods according to specified procedures and in compliance to EU GMP To prepare, standardise and label stock solutions and laboratory... ...be written in English. Please quote the vacancy name QA-RA Compliance Officer and number 417618 in your email. Latest...
- ...integrity, reporting accuracy, and system functionality Document test results, ensuring traceability and compliance with BEC’s QA standards Identify, report, and support the resolution of defects through structured QA processes Take ownership of the end...
- ...our products, and the belief that we are always trying to create better product for gamers, this might be the place for you. As a QA Engineer, you’ll play a key role in ensuring the quality and performance of our software and hardware products, working across multiple...
- ...Are you ready to play a key role in a newly established QA Validation team? Do you excel in quality assurance and thrive in challenging... ...and validation Understanding of Good Documentation Practices, GMP, Quality Systems, and pharmaceutical legislation Strong...
- ...We are searching for a QA Coordinator This position is based at our friendly office in Warsaw, and you will join our Financial Crime Prevention (FCP) program. We pursue the important mission to fight financial crime in collaboration with a wide range of Danish banks....
- ...Holbæk, Denmark Pharmacosmos International QA Director About the job International QA Director Join Pharmacosmos as they... ...rules for good manufacturing and distribution practices (GMP and GDP), and other relevant regulations. As such, you will oversee...
- ...Key accountabilities: • Manage the Oslo and Copenhagen QA team and strategy for critical projects • Analyze specific team testing requirements, execute and automate report on expected test cases to meet the quality department’s objectives • Create and execute component...
- ...care needs? And would you like to play a hand in the development of new innovative products? Then grab this opportunity to make your QA experience count as you work with products from initial idea all the way to market introduction. “You will be the advocate for...
- ...inspiring high-performing teams, this role offers an exciting challenge with considerable growth potential. Your new role As a senior QA professional in our Emerging Technologies QA team for Manufacturing Development, you will be instrumental in ensuring the quality and...
- ...clinical and commercial batches. You will liaison with the operational QA DS teams, DS Manufacturing Support, Process Science and QC on... ...the batch has been manufactured and tested in accordance with GMP regulations and quality agreements. To perform QP statements in...
- ...maintain high standards of quality? And would you like to support QA in tech transfer project for bringing new products from... ...to our start-up phase. We prioritize high-quality standards and GMP compliance through close collaboration with our stakeholders....
- ...as well as consulting on laboratory services in compliance with GMP and GLP standards. Job Description We are currently looking... ...experience in sales within the life science industry and/or experience in QA/Biosafety related to medical devices. ~ A science-based...
- ...på Masternivå Erfaring fra farmasøytisk industri, eller annen relevant industri eller offentlig tilsyn. God kjennskap til GMP og andre relevante lovverk og retningslinjer. Annet Evne til å kommunisere og samarbeide med kollegaer på alle nivå. Evne...
- ...reguleringsteknikk, mekanikk, maskin eller kalibrering. Relevant erfaring kan kompensere for manglende formell utdannelse. Erfaring med GMP/ farmasøytisk-, næringsmiddel eller prosessindustri, ISO 13485, FDA-reguleringer og kvalitetsstyringssystemer (QMS). God...
- ...Firmabeskrivelse Er du nyuddannet laborant eller har du et par års erfaring i et GMP laboratorie? Brænder du for mikrobiologi i et spændende og afvekslende arbejdsmiljø? Så har vi det rette job for dig! Eurofins BioPharma Product Testing Denmark A/S er et verdensførende...
- ...thought to finished implementation in production. And we manage the business with an uncompromising focus on quality based on current GMP requirements. Why join us? Potential to contribute shaping the future in a strategic, high-impact initiative. Competitive...
- ...Do you get excited when a Facility qualification is coming up? Then this might be your next job. You will be part of a world-class GMP manufacturing facility, and a leading CDMO where we advance tomorrow’s medicines today. About FUJIFILM Biotechnologies and our...
- ...report, AI on D365. C. WORKING RELATIONSHIP: 1. Internal: ü PPD workshop, Test center, Production unit. ü OM production, QA, QC, PPD, PM, CCD 2. External: None 3. Reporting: 3.1 Superior: Technical Manager, TD – R&D Senior Manager 3.2. Subordinate...
- ...laboratoriene våre vil du bli kjent med mange ulike instrumenter som for eksempel GC, HPLC, UPLC og IR. Et pluss er om du har erfaring fra GMP eller farmasøytisk industri fra tidligere. Det er vel så viktig at du har genuin interesse for kjemisk analyse, liker å dele...
- ...med prosessdesign og optimalisering fra farmasøytisk industri, næringsmiddel eller annen prosessindustri – gjerne med kjennskap til GMP. ~ God forståelse for prosesskontroll, risikoanalyser og teknisk dokumentasjon. ~ Erfaring med industriell regulering...
- ...Development Manufacturing Organization (CDMO) serving clients in the pharmaceutical industry – from pre-clinical investigations to commercial GMP production. Our overall mission is to “Advancing Tomorrow’s Medicines” and we like to invite you to be part of that journey. Our...
- ...process development, troubleshoot critical experiments, and validate key findings. Finally, you will collaborate with Quality Assurance (QA), Regulatory Affairs, Analytical, Manufacturing teams, CDMOs to align and support the development efforts with overall business...
- ...cost saving saving projects on key top runner C. WORKING RELATIONSHIP: 1. Internal: - PM, SALES VN/Sales, CDD, M-PPD, W-PPD, QA, PU and Production Units in SCVN. - Communicate TD - R&D Senior Manager directly on the daily job, the assigned projects and...
- ...ledelse. Er du den mindre erfarne profil, vil du også: Fokusere på dokumentation, afvigelseshåndtering og databehandling. Lære om GMP og produktionsunderstøttelse i et trygt og fagligt miljø. Få oplæring i vores udstyr og processer, bl.a. fermentering, filtrering...