Jobs / Switzerland / Novartis Pharmaceuticals Corporation

Novartis Pharmaceuticals Corporation

PHAD PDU Oral Drug Product Project Leader

Basel (City) Posted today

Apply on employer site ↗ Tailor my CV first Source: Company careers site

Optional: we can tailor a CV and cover letter for this job from your real experience first (the first one is free).

Sponsorship verdict

No sponsorship evidence yet

No government record and no wording either way. Not a refusal: ask the recruiter.

  • No government sponsor record hereNo government sponsor record covers this employer in this country.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • Can’t check pay against the visa rulesWe don’t have visa salary rules for this country yet.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

Before you apply

Sponsorship unknown

No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.

These come from the posting’s own wording. Read the original listing to confirm. See better-fit alternatives →

About the role

Salary Range: CHF93,800.00 - CHF174,200.00   Job Description Summary Location: Basel, Switzerland #onsite Role Purpose: We are looking for a collaborative and scientifically strong professional to take on the role of Drug Product Project Leader (DPPL) across late-phase oral drug product development programs. In this role, you will lead Drug Product technical development activities for assigned projects, ensuring scientific excellence, strong quality awareness, and alignment with overall project objectives. The role includes developing and implementing robust Drug Product project strategies, including risk assessments, contingency planning, timelines, budgets, and resource plans. It also requires ensuring alignment with internal functions, external partners, governance processes, and project review milestones. As DPPL, you will lead, coach, and develop high-performing project teams in line with company values and behaviors. The role is expected to foster a collaborative culture, promote knowledge sharing, set clear objectives, and support the growth and performance of team members. The position will oversee project execution, proactively manage cross-functional interfaces, and communicate project strategy, risks, issues, and critical updates to relevant stakeholders. Key responsibilities include ensuring high-quality development documentation and contributing to CMC submission packages, filing dossiers, inspection responses, and Health Authority requests. The role also includes acting as author, reviewer, or approver of development documents in accordance with applicable SOPs and development standards. In addition, the DPPL will drive Make versus Buy strategies and support outsourced activities with external partners, including input into contracts, quality agreements, and third-party supply-related projects.   Job Description Your responsibilities will include but are not limited to:    • Represent DP project teams within TRD sub-teams, providing strong quality awareness, scientific expertise, and technical leadership. • Develop robust DP project strategies, including contingency planning and risk assessments, while ensuring alignment with internal functions, external partners, and third parties • Assess, consolidate, and negotiate project resources, timelines, internal and external costs, and lead the budgeting process for DP activities. • Ensure adherence to project review processes and relevant governance boards, while implementing building on scientific excellence and approved DP strategies within the project team. • Proactively manage cross-functional project interactions, monitor project plans, ensure timely delivery of key outputs, and oversee high-quality DP development documentation for CMC submissions. • Understand and integrate scientific insight into how drug substance and excipient properties, formulation design, and process parameters influence product performance, manufacturability, and consistency.  • Support and apply structured, science-based approaches (e.g., quality-by-design, modelling, and digital tools) to enhance understanding, enable informed decision-making, and support consistent and efficient development practices  • Lead, manage, coach, and support DP teams in line with company values and behaviours, fostering collaboration, team spirit, knowledge sharing, and high performance. What you’ll bring to the role:    • Advanced degree in Pharmaceutical Technology, Powder Process Engineering, or a related scientific field; PhD or equivalent experience is valued.  • Minimum 5+ years of relevant industry experience in the development of pharmaceutical formulations, preferably with broad and profound understanding of development activities and processes in pharmaceutical sciences. (early and late pha

Apply on employer site ↗