cmc

At Nouryon, our global team takes positive action every day, to reach higher collectively and individually. We create innovative and sustainable solutions for our customers to answer society’s needs – today and in the future.We are looking for team members who bring ideas forward, champion others and work together to do better. Does that sound like you?...

A pharmaceutical development company is seeking a CMC Project Lead to join its team. This is an excellent opportunity for a biologics professional with several years of hands‑on experience who is ready to take on greater responsibility on client programmes.As Project Lead, you will act as the technical lead on each programme, serving as the client's...

Als Associate Researcher CMC werk je on-site in Leiden en voer je praktisch labwerk uit dat direct bijdraagt aan de ontwikkeling en karakterisering van therapeutische formuleringen. Je bereidt formuleringen, voert analytische metingen uit en legt nauwkeurig gegevens vast. De rol past goed bij een starter of junior met een achtergrond in analytische chemie,...

Nederlandse Voedsel- en Warenautoriteit (NVWA) zoekt een afdelingssecretaris voor de afdeling Communicatie, Media en Contact (CMC). Je bent de rechterhand van het afdelingshoofd en een sparringpartner voor het MT, met verantwoordelijkheid voor structuur in bedrijfsprocessen en integrale samenwerking.Je bewaakt planning en uitvoering, signaleert knelpunten en...

Advisor – Global Regulatory Affairs CMC Biologicals 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 support of the authorization and maintenance of registrations with global regulatory agencies for the biological...

Elanco is seeking an Advisor for Global Regulatory Affairs CMC Biologicals to lead regulatory CMC strategy across post-approval changes and geo-expansion. You will collaborate with R&D, Manufacturing, Quality, and regulatory partners to support registrations and lifecycle management of biological products.The role requires a science degree, deep EU vaccine...

Nouryon is seeking a CMC Quality Manager to drive and sustain site certifications supporting the growth of its CMC business. The role unites colleagues from diverse functions to align goals and ensure continuous improvement in regulated markets.You will lead audits, CAPA, and QMS activities, partnering with manufacturing sites and customers globally to...

Walker Cole International is seeking a CMC Project Lead for a pharmaceutical development company. The role is to act as the technical lead on client programmes across development to delivery, not a project management position.You will be the primary technical contact for clients, coordinating with process development, analytical and wider technical teams to...

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...

Amgen Breda is seeking a Regulatory Affairs Manager to lead site CMC regulatory activities for global submissions and post-market changes. You will collaborate with cross-functional teams and regulatory authorities to plan and execute site-specific regulatory strategies.The ideal candidate holds a Doctorate or Master’s degree (or a Bachelor’s with...

Kite Pharma seeks an experienced Regulatory Affairs CMC Lead to manage regulatory CMC deliverables for assigned cell therapy programs, ensuring alignment with EMA/EU requirements and RoW strategies. This is a senior, cross‑functional leadership role.The candidate should have 8+ years in Regulatory Affairs, advanced degrees (PhD/MS preferred), and strong...

GE HealthCare is seeking an API Lead to provide technical leadership for the development and manufacturing of APIs through external CMOs, from early development through commercialization. You will serve as the primary technical interface between internal project teams and external partners, ensuring quality, timelines, costs, and deliverables meet regulatory...

Advisor – Global Regulatory Affairs CMC Biologicals 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 support of the authorization and maintenance of registrations with global regulatory agencies for the biological products. ...

Advisor – Global Regulatory Affairs CMC Biologicals 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 support of the authorization and maintenance of registrations with global regulatory agencies for the biological products. ...

Elanco is seeking an Advisor for Global Regulatory Affairs CMC Biologicals to lead regulatory CMC strategy across post-approval changes and geo-expansion. You will collaborate with R&D, Manufacturing, Quality, and regulatory partners to support registrations and lifecycle management of biological products. The role requires a science degree, deep EU...

Elanco is seeking an Advisor for Global Regulatory Affairs CMC Biologicals to lead regulatory CMC strategy across post-approval changes and geo-expansion. You will collaborate with R&D, Manufacturing, Quality, and regulatory partners to support registrations and lifecycle management of biological products. The role requires a science degree, deep EU...

ROLE OVERVIEWAn exciting opportunity for a Regulatory Affairs Project Manager to join our client, a leading organisation within the pharmaceutical, biotechnology and life sciences sector. This role will lead and coordinate regulatory projects across the product lifecycle, working closely with Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC),...

Job Description SummaryAs API Lead, you provide technical leadership for the development and manufacturing of precursors and active pharmaceutical ingredients (APIs) through external Contract Manufacturing Organizations (CMOs). You lead activities from early development and process optimization through scale-up, technology transfer, GMP manufacturing, to...

Het Hoofd Cluster Coördinatie & Medezeggenschap van het Ministerie van Defensie geeft leiding aan een team van adviseurs en werkt nauw samen met andere clusters binnen de Directie HR. Je bent het klankbord tussen de directeuren en de rest van de organisatie en bewaakt een heldere koers en kwalitatief hoogwaardige adviesproducten.Daarnaast omvat de functie...

GE HealthCare is seeking an API Lead to provide technical leadership for the development and manufacturing of APIs through external CMOs, guiding activities from early development through scale-up and GMP manufacturing.You will act as the primary technical interface between internal project teams and external partners, ensuring quality, timelines, risks,...