cmc

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.Join Kite, as we make even...

Working with UsZorg ervoor dat u de volgende details zorgvuldig leest voordat u solliciteert.Challenging. Meaningful. Life-changing. Those aren’t 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...

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

Amgen Breda is seeking a Regulatory Affairs Manager to translate CMC regulatory requirements into practical plans and lead site-specific submissions.Controleer alstublieft of u het juiste niveau van ervaring en kwalificaties heeft door het volledige overzicht van deze vacature hieronder te lezen.The role includes coordinating post-market changes and...

The Principal Scientist, Chemistry, Manufacturing & Controls (CMC) Dossier Development, with some managerial guidance, develops the technical eCTD sections for Regulatory CMC dossier applications, coordinating and providing technical oversight for the generation of the CMC dossier of marketing and clinical trial submissions. Coordinates the timeline, virtual...

Lonza Oss (Synaffix) invites applications for a Development Manager II in the DAM department.Zorg ervoor dat al uw sollicitatiegegevens up-to-date en in orde zijn voordat u op deze vacature solliciteert.You will own development strategies, manage external manufacturing networks, and ensure reliable supply across clinical development and beyond.Collaboration...

Amgen Breda seeks a Regulatory Affairs Manager to translate CMC regulatory requirements into practical plans. You will manage site changes, coordinate with global authorities, and lead regulatory submissions for new marketing applications and post-market changes.The role requires strong leadership, English and Dutch communication, and experience in QA/RA...

Johnson & Johnson is seeking a Principal Scientist, Chemistry, Manufacturing & Controls (CMC) Dossier Development to lead regulatory dossiers and provide technical oversight for submissions. You will coordinate timelines, manage cross-functional teams, and ensure compliance with global regulatory requirements.The role requires strong expertise in CMC, eCTD...

Amgen Breda is seeking a Regulatory Affairs Manager to translate CMC regulatory requirements into practical plans. You’ll support site-specific CMC sections for new applications and post-market updates, lead change control and submissions, and coordinate with global authorities.The role requires a Doctorate/Master with 3+ years in pharma regulatory work or...

Advisor – Global Regulatory Affairs CMC BiologicalsDe volgende informatie is bedoeld om potentiële kandidaten een beter inzicht te geven in de vereisten voor deze functie.The purpose of the Advisor – Global Regulatory Affairs CMC Biologicals role is to work cross functionally with Elanco R&D, Manufacturing, Quality, and other Elanco departments in...

Amgen Breda is seeking a Regulatory Affairs Manager to translate CMC regulatory requirements into practical plans. You will support site-specific CMC sections for new marketing applications and post-market changes, coordinating with global regulators and internal teams.The role requires a Doctorate/Master’s with regulatory experience or a Bachelor’s with...

Leiden Bio Science Park is seeking a Principal Scientist, Chemistry, Manufacturing & Controls (CMC) Dossier Development to lead the technical eCTD sections for regulatory filings, coordinating the creation of CMC dossiers for marketing and clinical trial submissions.With managerial guidance, you will own dossier timelines, oversee cross-functional teams, and...

Barrington James is partnering with a growing pharmaceutical consultancy in the Netherlands to recruit an experienced Regulatory Affairs professional.Als u meer wilt weten over de vereisten voor deze functie, lees dan verder voor alle relevante informatie.The role covers a broad range of regulatory projects from early development to commercialization, with...

Kyowa Kirin International plc.Ontdek hieronder precies welke vaardigheden, ervaring en kwalificaties u nodig heeft om te slagen in deze functie, voordat u solliciteert.in Hoofddorp is seeking an Associate Director Global CMC QU – Clinical GMP/GDP to provide end-to-end QA oversight of clinical IMPs and ensure compliance with EU GMP Annex 13 and EU GDP...

OverviewOverviewSolliciteer nu, lees de vacaturedetails door naar beneden te scrollen. Controleer of u over de nodige vaardigheden beschikt voordat u een sollicitatie verstuurt.Associate Director Global CMC QU – Clinical GMP/GDPat Kyowa Kirin International plcMarlow, UK or Hoofddorp, NetherlandsWE PUSH THE BOUNDARIES OF MEDICINE.LEAPING FORWARD TO MAKE...

Bedrijfsomschrijving:Locatie: Assen. Deze organisatie is actief in de maakindustrie met een focus op de productie en ontwikkeling van middelen die worden toegepast binnen de gezondheidszorg en onderzoeksomgevingen. De organisatie ondersteunt projecten van vroege fase ontwikkeling tot aan productie en werkt intensief samen met interne laboratoria en...

Bristol Myers Squibb EU Policy is seeking a Senior Regulatory Affairs professional to guide CMC regulatory activities across development to lifecycle management in the EU region.Ligt uw cv klaar? Zo ja, en bent u ervan overtuigd dat dit de functie voor u is, zorg er dan voor dat u zo snel mogelijk solliciteert.The role requires coordinating with global...

Over Regivet Regivet BV is een gespecialiseerd adviesbureau voor de ontwikkeling en registratie van diergeneesmiddelen. Vanuit ons volledig uitgeruste laboratorium in Oirschot zijn de activiteiten gericht op de ontwikkeling van nieuwe diergeneesmiddelen, de productie ervan, het ontwikkelen en valideren van analysemethodes, stabiliteitsonderzoek en analyses...

**Over Regivet** Regivet BV is een gespecialiseerd adviesbureau voor de ontwikkeling en registratie van diergeneesmiddelen. Vanuit ons volledig uitgeruste laboratorium in Oirschot zijn de activiteiten gericht op de ontwikkeling van nieuwe diergeneesmiddelen, de productie ervan, het ontwikkelen en valideren van analysemethodes, stabiliteitsonderzoek en...

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make...