Drug Product Project Leader / Drug Product Project Leaderess

Novartis Pharma AG - July 30, 2025

Job ID

REQ-10051450

May 12, 2025

Switzerland

Summary

Location: Basel, Switzerland

Role Purpose: Join the Pharmaceutical Development (PHAD) Specialty Unit as an Associate Director - Drug Product Project Leader (DPPL) for drug product formulation and process development of parenteral innovative medicines, especially xRNA therapeutics and radioligand therapies (RLT). Advance the technology platform for both xRNA and RLTs and contribute to the development of patient-centric drugs. This position is perfect for an individual passionate about bringing transformational medicines to patients and working on exciting novel pharmaceutical products.

The PHAD Specialty Unit is seeking an experienced Drug Product Project Leader (DPPL) to lead DP development sub-teams, be accountable for the DP development project strategy, and represent DP development in the global CMC project team. Apply online using the form below and be a part of a team that is revolutionizing drug product development.

About the Role

Responsibilities

  • As Drug Product Project Leader, be the strategic lead of complex Drug Product Development projects (e.g., for Oligonucleotides or RLTs) within the PHAD Specialty Unit.
  • Lead and manage all formulation and process development activities for parenteral formulation development and manufacturing.
  • Represent DP project teams in global CMC teams, providing strong quality awareness, scientific expertise, and project management skills.
  • Develop a sound DP project strategy, including contingency planning and risk assessments, in line with the overall Technical R&D project plan and guidelines.
  • Monitor project plans and ensure timely availability of agreed timelines.
  • Contribute actively to network deliverables and cross-functional initiatives, promoting collaboration and knowledge sharing.
  • Act as an author, reviewer, or approver for PHAD-owned documents, supporting submission writing and addressing inspection requirements.
  • Ensure adherence to the EP/ LP project review process and maintain high-quality documentation through relevant governance boards.
  • Lead the Transfer Team and clinical development activities in alignment with TDP for late phase and LCM projects.
  • Lead and/or contribute actively to respective Network deliverables and cross-functional workstreams/initiatives.
  • Assess, consolidate, and negotiate resource needs (internal & external costs) and timelines. Lead budgeting process for DP activities.

Requirements

  • Ph.D. in Chemistry, Chemical Engineering, Pharmaceutical Technology, or related disciplines with 7+ years of industry experience in parenteral drug product development (e.g., for Oligonucleotides or Biologics), OR Master’s degree with 9+ years of biopharmaceutical industry experience.
  • Broad and profound understanding of development activities and processes in pharmaceutical sciences (parenteral, aseptic, solution, and/or suspension).
  • Strong knowledge of laboratory and/or technical tools (e.g., Quality by Design, statistical software, Process Analytical Technology).
  • Familiarity with devices such as pre-filling syringes, vials, and combination products is an advantage.
  • Strong scientific leadership skills.
  • Basic/Advanced skills in Data Analysis and Data Visualization, including the application of data science tools.
  • Strong knowledge of relevant GLP, GMP regulations, and policies requirements in parenteral Drug Product development and manufacturing.

Commitment to Diversity and Inclusion

Novartis is committed to building a diverse and inclusive work environment that reflects the patients and communities we serve.

Accessibility and Accommodation

Novartis is devoted to providing reasonable accommodations to all individuals. If, due to a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, please reach out via email to inclusion.switzerland@novartis.com with details of your request and contact information. Please include the job requisition number in your message.

Why Novartis

Helping people with disease and their families requires more than innovative science. It takes a community of smart, passionate individuals who collaborate, support, and inspire one another. Together, we can achieve breakthroughs that significantly improve patients' lives. Ready to create a brighter future together? Learn more.

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Benefits and Rewards

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Division

Development

Business Unit

Universal Hierarchy Node

Location

Switzerland

Site

Basel (City)

Company / Legal Entity

C028 (FCRS = CH028) Novartis Pharma AG

Functional Area

Research & Development

Job Type

Full time

Employment Type

Regular

Shift Work

No

Location : BASEL
Country : Switzerland

Application Form

Please enter your information in the following form and attach your resume (CV)

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