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Roche in Basel is seeking a Scientist in Pharmaceutical Development to lead end-to-end parenteral formulation and process development, from early-stage work to transfer to manufacturing. You will collaborate across global teams to drive regulatory submissions and product transfers.
The ideal candidate holds a PhD or Master in chemistry/related field with 2+ years of industry experience in parenteral DP formulation, and demonstrates curiosity for new modalities such as oligonucleotides.
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 to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
As a Scientist in Pharmaceutical Development, you are part of the Department "Pharmaceutical Development" in Pharma Technical Development (PTD) in Basel, Switzerland. The department Pharmaceutical Development is responsible for the development of parenteral drug products (Synthetic molecules and Biologics) from Phase 1 through market Launch. Activities encompass formulation and manufacturing process development for parenteral drug products for all clinical stages and the market launch, the transfer of product and process to commercial manufacturing sites, commercial product support and line extension development.
You will balance technical rigor in formulation and process development with an exploratory mindset, driving innovation in parenteral modalities, including Oligonucleotides and complex synthetic molecules. Lead the end-to-end development of parenteral formulations - liquid and lyophilized dosage forms - and establish robust manufacturing processes from scale-up and characterization to commercial transfer. Represent Pharmaceutical Development as a project leader in global CMC and cross-functional teams, providing critical technical expertise and strategic input for regulatory submissions (BLA/MAA/NDA) throughout all clinical stages. Actively apply creative, open-minded approaches to overcome unfavorable molecular properties. Serve as a key lab partner to Postdocs and Scientists to test and validate exploratory formulation concepts and new therapeutic modalities. Manage and support analytical method scouting, analytical understanding and implementation capabilities in our routine.
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