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Formulation Project Leader - Oral Dosage Forms (80-100%)

Entreprise
Novartis Pharma AG
Lieu
BASEL
Date
30.06.2025
Référence
132656

Opportunity Overview

Located in Basel, Switzerland, this role involves leading and managing the formulation and process development of Oral solid dosage forms from lab-scale through scale-up to commercial scale. The successful individual will work closely with the Drug Product Subteam, driving formulation activities with scientific excellence while employing data-driven methodologies.

Key Responsibilities

  • Passion for innovative formulations and experience in enabling formulation development.
  • Application of data-centric, computational models to guide formulation and manufacturing process development.
  • Oversight of the formulation development and manufacturing work of Oral Drug Products (NCE) driven by mechanistic modeling.
  • Close collaboration with the Drug Product Sub-Team and Transfer Team members to manage critical aspects related to Drug Substance, Drug Product, Analytics, Packaging, and Device.
  • Maintain regular communication with experts from Technology Focus Groups, Modelling & Simulation, and Biopharmaceutics to inform project strategy.
  • Authorship of comprehensive scientific development documents and GMP documents to facilitate commercial manufacturing of new Drug Products.
  • Contribution to the generation of CMC submission dossiers and support for Drug Product-related inquiries from Health Authorities and Inspectors.

Qualifications

  • Advanced degree (minimum PhD) in a relevant scientific field such as Pharmaceutical Technology or Chemical Engineering.
  • A minimum of 2 years of successful experience in pharmaceutical formulation development, focusing on small molecules.
  • Knowledge of data science and data visualization, with experience in applying computational models in product development.
  • Interdisciplinary thinking and an interest in collaboration across various functions.
  • Broad understanding of formulation development activities and technical knowledge of laboratory tools (e.g., QbD, PAT).
  • A strong familiarity with GLP, GMP regulations, and demonstrated problem-solving skills.
  • Effective communication, planning, and negotiation abilities alongside strong scientific writing skills.

Commitment to Diversity and Inclusion

We are dedicated to fostering an inclusive work environment and building diverse teams that represent the patients and communities we serve.

Why Join Us?

Our community is comprised of passionate individuals who collaborate to achieve breakthroughs that enhance patients' lives. Together, we are committed to creating a brighter future in healthcare.

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To learn more about our benefits and the ways we support personal and professional growth, please visit our benefits and rewards page.

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