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Scientist Pharmaceutical and Processing Development

Job in 4040, Basel, Kanton Basel-Landschaft, Switzerland
Listing for: Roche Holding AG
Contract position
Listed on 2026-08-28
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 120000 - 150000 CHF Yearly CHF 120000.00 150000.00 YEAR
Job Description & How to Apply Below
Position: Scientist Pharmaceutical and Processing Development (2 year fixed term contract)

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. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir.

Rejoignez Roche, où chaque voix compte.

La position

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.

The Opportunity

  • Lead the end-to-end development of parenteral formulations—including 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.

Who you are
  • You hold a Ph.D. or master degree in chemistry, chemical/process engineering or related fields and bring a minimum of 2 years of professional experience (industry) in formulation and process development DP manufacturing related fields of parenteral dosage forms.

  • Eagerness to Learn & Grow:
    Strong intrinsic motivation to master new therapeutic modalities, specifically building a deep technical footprint in Oligonucleotide formulation and analytical-formulation loops.

  • Technical Agility & Curiosity:
    Comfort in or a strong motivation to acquire knowledge and advance in unfamiliar fields, particularly digital domains. A natural inclination to challenge the status quo and show curiosity.

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