Drug Product Project Leader - Oral Dosage Forms (80-100%*)
- Entreprise
- Novartis Pharma AG
- Lieu
- BASEL
- Date
- 22.09.2025
- Référence
- 178493
Location
Basel, Switzerland
Role Overview
Join a leading team dedicated to innovative pharmaceutical development. This role focuses on overseeing formulation and manufacturing activities for small molecules, specifically tailored to create patient-centric oral dosage forms. Leveraging your expertise in applied data science and mechanistic modeling, you'll manage project teams through the critical initial phases of the clinical development process.
Responsibilities
Your key responsibilities will include:
- Leading and managing all technical development activities related to drug products for assigned projects, representing project teams effectively in sub-teams.
- Fostering a collaborative team environment, promoting knowledge exchange, and coaching team members to achieve high performance aligned with company values.
- Formulating and executing project strategies, including risk assessments and resource planning, in alignment with internal and external stakeholders.
- Ensuring the scientific integrity of development documents and adherence to governance processes, facilitating successful CMC submissions.
- Contributing to regulatory filings and supporting inquiries from health authorities.
Qualifications
To be successful in this role, you will bring:
- An advanced degree in a relevant scientific discipline such as Pharmaceutical Technology or Chemistry.
- A minimum of 2-4 years of industry experience in pharmaceutical formulation development in a matrix organization.
- Proven expertise in biopharmaceutical sciences, including knowledge of physical-chemical properties of molecules and their in-vivo performance.
- Strong project management and problem-solving skills, with proficiency in organizational and negotiation capabilities.
- A collaborative mindset and a comprehensive understanding of pharmaceutical development processes.
- Familiarity with laboratory and technical tools, alongside relevant GLP and GMP regulations.
- Exceptional presentation abilities and proficiency in scientific and technical writing.
Commitment to Inclusion
The organization is dedicated to fostering a diverse and inclusive environment that reflects the communities and patients it serves. A strong emphasis is placed on providing accommodations that support all individuals effectively.
Why Join Us?
Be part of a passionate community committed to transforming lives through science and innovation. Together, we can achieve remarkable breakthroughs that positively impact patient care and make a meaningful difference. Explore opportunities for professional growth and contribute to a brighter future.
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Benefits and Rewards
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