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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