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TryHire is seeking a senior specialist to develop manufacturing processes for parenteral liquid and lyophilized formulations in Basel. You will lead process characterization, design studies, and drive technology transfer to global commercial sites while coordinating with cross-functional teams.You will author drug product sections of NDA/BLA submissions and...

Roche in Basel, Switzerland, invites an experienced Principal Process Engineer to join Pharmaceutical Development within PTD. You will lead parenteral process development from Phase 1 through Launch, focusing on robust manufacturing, scale-up, and transfer to global sites.You will design process characterization studies, represent DP process development in...

pGi Group is seeking a Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR) to lead global regulatory submissions and manage CMC information for IND, IMPD, and NDA/BLA/MAA filings. The role collaborates with affiliates, policy teams, and partners on early clinical stage programs and IMPD submissions. /ppThe ideal candidate has 3–4 years of CMC...

The role develops robust manufacturing processes for parenteral drug products, from process characterization to technology transfer and commercial launch. Your tasks Develop manufacturing processes for parenteral liquid and lyophilized formulations Design and execute process characterization and process design studies Lead technology transfer projects to...

pIn the position of Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR), you will be accountable for handling all Health Authority interactions pertaining to CMC Information (for example in an IND, IMPD and NDA/BLA/MAA filings), as well as informational and/or pre-submission meetings with global Health Authorities, partners and industry experts....

Senior Expert Container Closure Systems (m/f/d, fix or freelance, 100%)Your ResponsibilitiesLead the technical development of combination products and medical devices from concept through commercializationDefine and assess primary packaging solutions, applying expertise in Type I glass, COP/COC polymers, elastomers, coatings, and extractables leachables...

pIn the position of Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR), you will be accountable for handling all Health Authority interactions pertaining to CMC Information (for example in an IND, IMPD and NDA/BLA/MAA filings), as well as informational and/or pre-submission meetings with global Health Authorities, partners and industry experts....

ph3Overview /h3pMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory filings....

OverviewMonte Rosa Therapeutics is seeking a highly skilled and self-motivated regulatory professional to join our team as an Associate Director of CMC Regulatory Affairs. The CMC Regulatory Affairs will serve as a key regulatory strategist and author for the Chemistry, Manufacturing, and Controls components of Monte Rosa's global regulatory filings. This...

The role develops robust manufacturing processes for parenteral drug products, from process characterization to technology transfer and commercial launch.TasksDevelop manufacturing processes for parenteral liquid and lyophilized formulationsDesign and execute process characterization and process design studiesLead technology transfer projects to global...

pChez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement....

ppAt 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 to prevent, stop and cure diseases and ensure...

Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement....

pBei Roche kannst du ganz du selbst sein und wirst für deine einzigartigen Qualitäten geschätzt. Unsere Kultur fördert persönlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du für das, was du bist, wertgeschätzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl persönlich als auch beruflich wachsen kannst....

ppAt 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 to prevent, stop and cure diseases and ensure...

pAt 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 to prevent, stop and cure diseases and ensure...

pSalary Range: /brpCHF126,000.00 - CHF234,000.00 /p /br /brJob Description Summary /brp#LI-Hybrid /p /brpLocation: Basel, Switzerland /p /brpThis role is based in Basel, Switzerland. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you. /p /br /brpWe are a global team of highly...

Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement....

CARBOGEN AMCIS AG in Bubendorf, Switzerland, seeks a Manager RAC (Regulatory Affairs CMC) to support Drug Substance CMC projects and small molecules/ADCs. You will coordinate regulatory activities from development to market launch, and provide internal/external regulatory guidance.You will author/regulate IND/IMPD/MAA/BLA submissions, manage post-approval...

Monte Rosa Therapeutics, Inc is seeking an Associate Director of CMC Regulatory Affairs to lead global regulatory strategies for Chemistry, Manufacturing, and Controls across development stages. You will author Module 3 content, review summaries, and partner with Process Chemistry, Analytical Development, Drug Product, Quality, and Clinical Supply teams to...