qa associate

Wat ga je doenAls QA Associate ben je verantwoordelijk voor het beoordelen en bewaken van kwaliteitsprocessen binnen een technisch georiënteerde farmaceutische omgeving. Je zorgt ervoor dat productieapparatuur, laboratoriuminstrumenten, facilities en utilities voldoen aan de geldende GMP-richtlijnen. Daarbij beoordeel je kwalificatiedocumentatie en...

Wat ga je doenIn de rol van QA Associate richt je je op het waarborgen en verbeteren van kwaliteit binnen een GMP-gereguleerde productieomgeving. Je controleert of procedures correct worden gevolgd, beoordeelt kwaliteitsdocumentatie en ondersteunt bij onderzoeken naar afwijkingen en non-conformiteiten. Daarbij werk je samen met collega’s van productie,...

Senior QA Associate – Pharmaceutical Industry Breda, reference 2026-01228 Job description As a Senior Quality Assurance Associate – Clinical Supply Chain, you will be responsible for ensuring that medicines used in clinical trials meet the required quality and regulatory standards.You will oversee quality processes related to the packaging, labelling,...

As a Senior Quality Assurance Associate – Clinical Supply Chain, you will be responsible for ensuring that medicines used in clinical trials meet the required quality and regulatory standards.Wilt u solliciteren? Lees alle informatie over deze functie hieronder en klik dan op de sollicitatieknop.You will oversee quality processes related to the packaging,...

As a strongSenior Quality Assurance Associate – Clinical Supply Chain /strong, you will be responsible for ensuring that medicines used in clinical trials meet the required quality and regulatory standards.br /You will oversee quality processes related to the packaging, labelling, storage and distribution of clinical trial products. You will also work...

As a strongSenior Quality Assurance Associate – Clinical Supply Chain /strong, you will be responsible for ensuring that medicines used in clinical trials meet the required quality and regulatory standards.br /You will oversee quality processes related to the packaging, labelling, storage and distribution of clinical trial products. You will also work...

As a Senior Quality Assurance Associate – Clinical Supply Chain , you will be responsible for ensuring that medicines used in clinical trials meet the required quality and regulatory standards. You will oversee quality processes related to the packaging, labelling, storage and distribution of clinical trial products. You will also work closely with...

As a Senior Quality Assurance Associate – Clinical Supply Chain , you will be responsible for ensuring that medicines used in clinical trials meet the required quality and regulatory standards. You will oversee quality processes related to the packaging, labelling, storage and distribution of clinical trial products. You will also work closely with...

As a Senior Quality Assurance Associate – Clinical Supply Chain, you will be responsible for ensuring that medicines used in clinical trials meet the required quality and regulatory standards. You will oversee quality processes related to the packaging, labelling, storage and distribution of clinical trial products. You will also work closely with...

pbloomon is turning the flower industry on its head – for the better. How? By disrupting the traditional supply chain! We skip the auction and wholesale, to shorten the journey for our flowers. And we harness technology, brand and innovation to deliver gifts and subscriptions that delight our customers across Europe. /p pWe launched in Amsterdam in 2014,...

pbloomon is turning the flower industry on its head – for the better. How? By disrupting the traditional supply chain! We skip the auction and wholesale, to shorten the journey for our flowers. And we harness technology, brand and innovation to deliver gifts and subscriptions that delight our customers across Europe. /p pWe launched in Amsterdam in 2014,...

pbBuild the quality standards that help deliver life-saving medicines. /b /ppAlcami is a leading global Contract Development and Manufacturing Organization (CDMO), providing integrated solutions to the pharmaceutical and biotechnology industries. We support our customers across the pharmaceutical lifecycle with a shared purpose: helping bring important...

pbBuild the quality standards that help deliver life-saving medicines. /b /ppAlcami is a leading global Contract Development and Manufacturing Organization (CDMO), providing integrated solutions to the pharmaceutical and biotechnology industries. We support our customers across the pharmaceutical lifecycle with a shared purpose: helping bring important...

pReal is seeking a Senior Associate Quality Assurance (QA) to support quality operations in Breda, Netherlands. This role focuses on GMP-compliant QA activities, SAP Master Data review, artwork approval, and SOP management within a regulated pharmaceutical manufacturing environment. /ppYou will collaborate with Global Artwork Centre, Master Data, Regulatory...

pReal is seeking a Senior Associate Quality Assurance (QA) to support quality operations in Breda, Netherlands. This role focuses on GMP-compliant QA activities, SAP Master Data review, artwork approval, and SOP management within a regulated pharmaceutical manufacturing environment. /ppYou will collaborate with Global Artwork Centre, Master Data, Regulatory...

pPeople in Science in Breda seeks a Senior Associate Quality Assurance to provide QA oversight of both clinical manufacturing and clinical supply chain activities. You will support labelling, packaging, and documentation reviews while ensuring GMP/GDP compliance and coordinating with Production, Warehouse, Supply Chain and Regulatory Affairs. /ppIdeal...

pPeople in Science in Breda seeks a Senior Associate Quality Assurance to provide QA oversight of both clinical manufacturing and clinical supply chain activities. You will support labelling, packaging, and documentation reviews while ensuring GMP/GDP compliance and coordinating with Production, Warehouse, Supply Chain and Regulatory Affairs. /ppIdeal...

pPanda International in Breda, the Netherlands, seeks a detail-oriented QA professional to support GMP-compliant master data and artwork processes. You will review and approve SAP master data, ensure QA systems are maintained, and collaborate with the Global Artwork Center, Master Data, and site SMEs. /ppKey responsibilities include approving BOMs and...