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Global head dp development & technology

Barberà del Vallès
Siegfried
Publicada el 13 marzo
Descripción

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long‐term opportunities to grow and make an impact.

Your RoleIn this newly created role, you will lead the global Drug Product (DP) Development organization and further strengthen Siegfried's pharmaceutical development capabilities. You will drive the advancement of Siegfried's DP technologies and development project performance across all clinical phases. You will ensure best-in‐class pharmaceutical R&D processes covering multiple dosage forms, including oral solid dosage forms, parenterals, inhalables, and ophthalmics. The role includes evaluating new customer development requests for formulation and process development, overseeing execution of development programs, and ensuring successful transfer to GMP manufacturing. In addition, you will build and expand the organization's capabilities by attracting, developing, and mentoring top DP development talent across sites.

In that role, you will

Lead and manage the global Drug Product Development & Technologies function, with oversight of pharmaceutical development, characterization capabilities, and development project execution from preclinical development through Phase III and commercialization.

Lead the inquiry‐to‐offer process for new client development requests, ensuring high‐quality, scientifically robust and competitive development proposals through strong technological evaluation and efficient decision making.

Oversee the multi‐site execution of Siegfried's 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.

Technical profile

Pharmacist or equivalent scientific background; PhD in Pharmaceutical Technology preferred

Extensive expertise in oral solid dosage form development, including technologies for BCS Class II and III compounds

Experience with advanced formulation technologies, such as amorphous solid dispersions; experience with inhalation products is advantageous

Strong expertise in parenteral dosage form development; experience in ophthalmic formulations is beneficial

Deep knowledge of analytical characterization of oral solid 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

Leadership profile

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

Your BenefitsAt Siegfried, you'll find more than just a job – you'll discover a place where your impact matters, your growth is encouraged, and your wellbeing is supported.

Professional Growth & Impact

You'll find a dynamic, international environment with room to take ownership and make a long‐term sustainable impact.

You'll be able to build and shape the function

Through your impact and Individual development solutions you'll grow personally and professionally at a fast pace.

You'll collaborate with an experienced, passionate teams that values excellence, quality and continuous learning.

Attractive Compensation & Incentives

Short‐term incentive programs recognizing both performance and contribution

Long‐term incentive plan focused on sustained value creation

Flexibility & Wellbeing

Flexible working hours and hybrid work options.

Comprehensive accident and health insurance coverage.

Active health management and discounted fitness memberships.

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know‐how and experience makes us the most trusted partner in the pharmaceutical industry.

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Qa operations admin - flexible hours & growth opportunities - siegfried ltd
Barcelona
Siegfried Ltd
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Empleo Barberà del Vallès
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