Regulatory Affairs Jobs in Poland
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Pharmacovigilance Lead Aggregate Reporting
Med Communications International
Pharmacovigilance Lead Aggregate Reporting Position Summary The PV Aggregate Reporting Lead is a senior expert responsible for leading coordinating and overseeing the preparation and submission of aggregate safety reports across assigned client portfolios. The role encompasses the full lifecycle of...
Pharmacovigilance Manager Benefit Risk
Med Communications International
Pharmacovigilance Manager Benefit RiskPosition Summary The Pharmacovigilance (PV) Manager Benefit Risk is a senior safety professional responsible for leading and overseeing benefit-risk evaluation activities across assigned products and client portfolios. This role ensures the continuous assessme...
Domain Architect Pharma R&d
Roche
At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...
Regulatory Affairs Manager, Cisasia Cluster, Em Pa...
Gsk
At GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform peoples li...
Specialist, Regulatory Affairs
Iff
Job SummaryAre you ready to take your skills to the next level and make a real impactIFF is a global leader in flavors fragrances food ingredients and health & biosciences we deliver sustainable innovations that elevate everyday products.Food Ingredients: Innovating improved nutritional profiles bet...
Director, Ai Product Owner
Astrazeneca
Location: Warsaw PolandHybrid model of work: 3 days in office 2 remote per weekTransform clinical trials through AI.Join AstraZenecas Emerging Technologies team to pioneer intelligent solutions that accelerate life-saving therapies optimize global study delivery and redefineClinical Operations.As Di...
Global Artwork Director Suppliers & Pmo
Sandoz
Job Description SummarySandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. By creating a new and ambitious path it will provide a unique opportunity for us all both professionally and personally. Jo...
Senior Regulatory Affairs Specialist (fixed-term C...
Stryker
Work Flexibility: HybridWhat You Will Do:Support product notification and market access activities for Stryker PolskaMaintain accuracy of data in Stryker regulatory databases and in the local ERP systemProvide regulatory documentation to tenders distributors and customersCommunicate regulatory chang...
Sr Brand Manager, Hcp
Abbott
JOB DESCRIPTION:Abbottis a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.Working atAbbottAtAbbott you can do work that matters grow and learn care for yourself and fami...
Regulatory Executive (eurasia)
Gsk
At GSK we unite science technology and talent to get ahead of disease together.As a Regulatory Executive you will provide operational regulatory leadership and coordination across assigned markets working closely with regional teams content delivery partners and thirdparty service providers. You wil...
Regulatory Affairs Associate
Alcon Research
At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 associates we innovate fearlessly champion progress and act swiftly to impact global eye health. We foster an inclusive culture recognizing your contributions and offering opportunities to grow yo...
Medical Information Client Manager Team Lead (germ...
Eversana
THE POSITION: Medical Information is a critically important customer-facing function that supports the safe and effective use of pharmaceutical company products by providing timely scientifically balanced evidence based non-promotional information in response to unsolicited requests from healthcare...
Senior Manager, Regulatory Asset Oversight
Gsk
The Senior Manager Regulatory Asset Oversight will partner with the GRL and Regulatory Matrix Teams (RMT) and Early/Medicine Development Teams to provide over-arching project management support to active Rx and Vx projects across the lifecycle of the asset. As Senior Manager Regulatory Asset Oversig...
Medical Manager
Novo Nordisk
Medical & RegulatoryWarszawa PolskaDołącz do Zespołu Medycznego pracującego z szybko rozwijającym się portfolio kardiometabolicznym i kształtuj przyszłość opieki nad pacjentami w całej Polsce dostarczając przełomowe terapie tym którzy najbardziej ich potrzebują.Twoja nowa rolaJako Medical Manager d...
Regulatory Affairs Associate
Colgate
No Relocation Assistance OfferedJob Number#172184 - Warsaw Mazovia PolandWho We AreColgate-Palmolive Company is a global consumer products company operating in over 200 countries specialising in Oral Care Personal Care Home Care Skin Care and Pet Nutrition. Our products are trusted in more household...
Senior Specialist Regulatory Affairs
Abbott
JOB DESCRIPTION:Abbottis a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.Working atAbbottAtAbbott you can do work that matters grow and learn care for yourself and fami...
Technical Program Manager
Motorola Solutions
Company OverviewAt Motorola Solutions we believe that everything starts with our people. Were a global close-knit community united by the relentless pursuit to help keep people safer everywhere. We build and connect technologies to help protect people property and places. Our solutions foster the co...
Senior Manager, Pv Process Quality Lead
Bristol Myers Squibb
Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...
Senior Technical Writer Information Architect
Demant
You will create and structure Instructions for Use (IFU) for hearing aid devices using a modern structured content platform (AEM Guides / DITA XML) working closely with R&D and Regulatory teams in Denmark and Poland.When you join the Demant family you become part of a world-leading hearing healthca...
Complaint Handling Specialist With Eu Language
Alcon Research
At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 associates we innovate fearlessly champion progress and act swiftly to impact global eye health. We foster an inclusive culture recognizing your contributions and offering opportunities to grow yo...