Vacatures pharmaceutical in Almere

Olivi.Growth is looking for a Project Manager Medical Construction in Flevoland, Netherlands. You will oversee medical projects from initiation to delivery, ensuring quality, planning, and compliance with regulations.Overweegt u te solliciteren op deze baan? Controleer alle details in deze functieomschrijving en klik vervolgens op \'Solliciteren\'.The ideal...

A pharmaceutical company in Almere, Netherlands is seeking a Pharmacovigilance & Regulatory Affairs Officer to support key safety and registration processes within a regulated environment.U kunt meer details krijgen over de aard van deze vacature en wat er van sollicitanten wordt verwacht door hieronder te lezen.The ideal candidate must be fluent in Dutch...

Having the best product in the world will not help you unless you can communicate it.Als u overweegt een sollicitatie te sturen, zorg er dan voor dat u op de sollicitatieknop hieronder klikt na het lezen van de gehele omschrijving.At Pharma Nord, we know this well, which is why we strive to create impactful and informative marketing that ensures our products...

Our client is a leading specialist in the design and realisation of classified medical buildings and spaces. Operating across hospitals, clinics, independent treatment centres and pharmaceutical facilities, they deliver complex projects ranging from operating rooms and cleanrooms to complete medical buildings — using both traditional and modular...

Product TrainerSolliciteer nu, lees de vacaturedetails door naar beneden te scrollen. Controleer of u over de nodige vaardigheden beschikt voordat u een sollicitatie verstuurt.Join to apply for the Product Trainer role at Pharma Nord Nederland.Pharma Nord is looking for a Product Trainer to support health professionals in the South of the Netherlands. This...

Sinclair is Hiring! Join Our Team as a [ Insert Job Title] 🚀We are currently recruiting for [ Insert Job Title] at [Insert location]. The [ Insert Job Title] will have [add details about the vacancy].Planning & Inventory ManagerLocationAlmere, NetherlandsDepartmentOperationsEmployment TypeFull-time contractOffice-basedLocal scopeReports ToPlant...

Working hours: 40 (possible to work from home 2 days), PV 20 hours & RA 20 hoursHeeft u de juiste vaardigheden en ervaring voor deze functie? Lees verder om erachter te komen en dien uw sollicitatie in.Department: MedicalReports to: Quality and Regulatory Affairs ManagerPosition SummaryAs Pharmacovigilance & Regulatory Affairs Officer you will supports the...

Sinclair is Hiring! Join Our Team as a Global Import/Export Expert 🚀We are currently recruiting for Global Import/Export Expert at our offices in Almere, Netherlands. As the Global Import/Export Expert at Sinclair, you will own end-to-end customs logistics management, compliance and cross-border trade operations for our global supply chain. You will...

Job Description SummaryJoin us, the future is ours to shape!Alle kandidaten dienen de volgende functieomschrijving en informatie zorgvuldig te lezen alvorens te solliciteren.Job DescriptionYour Key Responsibilities:Developing evidence-based policy positions for regulatory requirements for ethical and efficient development and manufacturing of generic and...

Sinclair is Hiring! Join Our Team as Chief Development Officer. Location: Flexible across Europe (Preferred: Netherlands, UK, Germany, Italy, Spain or France) Role Purpose The Chief Development Officer (CDO) is a member of the Executive Leadership Team and is responsible for leading the Company's global Quality, Regulatory Affairs, Vigilance and Product...

As a Regulatory Affairs Specialist at Sandoz, you will work on registrations, product information and artworks for existing and future products. You combine attention to detail with strong planning skills and collaborate with a range of internal and external stakeholders. What will you do? As a Regulatory Affairs Specialist, you ensure that our products...

The Operations Publishing team is responsible for the delivery of published output which fulfils the technical and format requirements of the Health Authorities and is dispatched and / or submitted to the authorities according to given timelines and in high quality. of regulatory application cluster in terms of first level issue, change and user...

Your responsibilities include, but not limited to: Developing evidence-based policy positions for regulatory requirements for ethical and efficient development and manufacturing of generic and biosimilar medicines. Aligning Sandoz policy objectives and advocacy plans within Sandoz and within the trade association to shape emerging legislative proposals and...

Overview Als u meer wilt weten over de vereisten voor deze functie, lees dan verder voor alle relevante informatie.PM Group are seeking an experienced Turnover Coordinator to join our pharma construction project team in Geel, Belgium. PM Group is an employee owned, international project delivery firm. We are world leaders in the pharma, food, medtech and...

Job Description SummaryAt Sandoz, our Purpose is pioneering access for patientsJob DescriptionAs a Regulatory Affairs Specialist at Sandoz, you will work on registrations, product information and artworks for existing and future products. You combine attention to detail with strong planning skills and collaborate with a range of internal and external...

Job Description SummaryJoin us, the future is ours to shape!Job DescriptionThe Operations Publishing team is responsible for the delivery of published output which fulfils the technical and format requirements of the Health Authorities and is dispatched and / or submitted to the authorities according to given timelines and in high quality. of regulatory...

Overview Zorg ervoor dat u solliciteert met alle gevraagde informatie, zoals uiteengezet in het functieoverzicht hieronder.The Architect position is an exciting opportunity to join PM Group’s quickly growing Benelux team. We will all be sharing knowledge, learning, growing, and continuing to be an integral part of supporting PM Group’s ongoing expansion...