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Global Head Drug Product Development & Technology

Siegfried · Zofingen

Siegfried seeks a Director to lead global Drug Product Development, advancing pharmaceutical technologies across multiple dosage forms and clinical phases while building a high-performing international team.

The company is looking for a Director to head the global Drug Product Development organization. This role focuses on strengthening Siegfried’s pharmaceutical development capabilities, advancing development project performance across clinical phases, and ensuring best-in-class R&D processes for various dosage forms.

Responsibilities

  • Direct the global Drug Product Development & Technologies function, overseeing pharmaceutical development, characterization capabilities, and project execution from preclinical stages through commercialization.
  • Manage the inquiry-to-offer process for new client development requests, ensuring high-quality, scientifically robust, and competitive development proposals.
  • Oversee the multi-site execution of the global development project portfolio, ensuring scientific excellence, timely execution, and strong customer outcomes.
  • Monitor scientific and technology trends to identify emerging formulation technologies, services, and development opportunities.
  • Strengthen Siegfried’s reputation as a leading Drug Product Development partner for pharmaceutical and biotech clients.
  • Develop and maintain global DP technology roadmaps across development phases, sites, and dosage forms.
  • Collaborate closely with key internal stakeholders including Business Development & Sales, manufacturing sites, and other global functions.
  • Build, mentor, and develop a high-performing global team, attracting and nurturing top scientific talent.

Requirements

  • Pharmacist or equivalent scientific background.
  • Deep expertise in oral solid dosage form (OSD) and parenteral development is essential.
  • Proven track record of advancing OSD and/or parenteral programs from early development through clinical phases to commercialization.
  • Strong understanding of analytical characterization and CMC development for OSD and parenteral dosage forms.
  • Deep expertise in CMC development, preferably within Drug Product Development.
  • With demonstrated track record advancing development programs from early research through clinical development and product launch.
  • Experience contributing to or generating Drug Product intellectual property.
  • Strong academic network and experience with public-private collaborations.
  • Proven ability to build and lead global teams across multiple sites.
  • Strong cross-cultural leadership and global mindset.
  • Experience working effectively in complex matrix organizations.
  • Ability to influence stakeholders in multi-site environments with indirect reporting structures.

Nice to have

  • PhD in Pharmaceutical Technology preferred.
  • Working knowledge and/or strategic oversight of additional dosage forms (e.g., inhalation, ophthalmic) is advantageous.

What the company offers

  • Dynamic, international environment with room to take ownership and make a long term sustainable impact.
  • Ability to build and shape the function.
  • Individual development solutions to grow personally and professionally at a fast pace.
  • Collaboration with an experienced, passionate teams that values excellence, quality and continuous learning.
  • Short-term incentive programs recognizing both performance and contribution.
  • Long-term incentive plan focused on sustained value creation.
  • Flexible working hours and hybrid work options.
  • Comprehensive accident and health insurance coverage.
  • Active health management and discounted fitness memberships.

About the company

Siegfried upholds the highest standards in safety, quality and sustainability. Fostering a culture that empowers you to thrive. A rapidly expanding global company where diverse perspectives and experiences come together in a collaborative environment. A workplace that values both collective success and your individual contributions. A fully integrated CDMO that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. The most trusted partner in the pharmaceutical industry.

  • Siegfried upholds the highest standards in safety, quality and sustainability.
  • Fostering a culture that empowers you to thrive.
  • A rapidly expanding global company where diverse perspectives and experiences come together in a collaborative environment.
  • A workplace that values both collective success and your individual contributions.
  • A fully integrated CDMO that can carry out the development and manufacturing of APIs and finished dosage forms under one roof.
  • The most trusted partner in the pharmaceutical industry.

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