Auf einen Blick
- Aufgaben: Leite ein Team zur Entwicklung innovativer biopharmazeutischer Formulierungen und Prozesse.
- Unternehmen: Führendes globales Unternehmen in der biopharmazeutischen Forschung.
- Vorteile: Strategische Einflussnahme, internationale Sichtbarkeit und Führungsverantwortung.
- Weitere Informationen: Hochinnovatives Umfeld mit exzellenten Karrierechancen.
- Warum dieser Job: Gestalte die Zukunft fortschrittlicher Therapien für unbefriedigte medizinische Bedürfnisse weltweit.
- Qualifikationen: PhD oder Master in relevanten Disziplinen mit umfangreicher Branchenerfahrung.
Das prognostizierte Gehalt liegt zwischen 85500 - 104500 € pro Jahr.
Location
Germany |
Industry
Innovative Biopharmaceuticals |
Leadership Level
- Senior Management
- A leading global biopharmaceutical organization is seeking an experienced
CMC Lead Formulation Development to provide scientific, strategic, and people leadership within a cutting‑edge research and development environment.
This role offers the opportunity to drive formulation and process development for advanced biologics, including antibody‑drug conjugates (ADCs), while playing a key role in global development programs from early‑stage development through commercialization.
Key Responsibilities
- Lead and develop a highly skilled formulation development team, providing both technical and people leadership.
- Drive formulation design, process development, and manufacturing strategy for complex biologic products and novel therapeutic modalities.
- Establish robust manufacturing processes, control strategies, and product formulations to support successful clinical and commercial development.
- Lead technology transfer activities to internal manufacturing sites and external CDMO partners across Europe.
- Oversee clinical trial material (CTM) manufacturing activities and ensure execution in line with quality, regulatory, and project requirements.
- Support lifecycle management initiatives for commercial products and contribute to ongoing product optimization.
- Provide strategic CMC leadership for global development programs, including preparation and support of regulatory submissions such as INDs, NDAs, BLAs, and post‑approval variations.
- Collaborate with multidisciplinary global teams across R&D, Regulatory Affairs, Quality, Manufacturing, and Supply Chain.
- Develop and execute departmental strategies, annual operating plans, resource allocation, and performance objectives.
- Mentor and develop scientific talent while fostering a high‑performing, inclusive, and innovative team culture.
Qualifications
- Ph D in Pharmacy, Pharmaceutical Sciences, Life Sciences, Engineering, or a related discipline; alternatively a Master's degree with substantial relevant industry experience.
- Extensive pharmaceutical industry experience (typically 10+ years) in formulation development, CMC development, biologics development, or related functions.
- Proven track record in product development and successful advancement of pharmaceutical programs from development through commercialization.
- Strong understanding of global CMC requirements, formulation sciences, technology transfer, GMP regulations, and quality systems.
- Demonstrated experience supporting or leading major regulatory submissions, including BLA filings.
- Previous line management experience with responsibility for team development and performance management.
- Strong leadership, stakeholder management, and communication skills.
- Experience operating successfully within complex global matrix organizations.
- Fluency in English, both written and spoken.
Why This Opportunity?
This is an exceptional opportunity to join a highly innovative biopharmaceutical company at the forefront of next‑generation therapies.
The position offers significant strategic influence, international visibility, leadership responsibility, and the chance to shape the future of advanced medicines that address serious unmet medical needs worldwide.
- Desired Skills and Experience
- Formulation Development
- Drug Product Development
- Pharmaceutical Development
- Biologics Development
- Antibody Drug Conjugates (ADC)
- Bioconjugates
- Protein Formulation
- Sterile Formulation
- Injectable Development
- Parenteral Drug Products
- Lyophilization
- Drug Product CMC
- Product Development
- Pharmaceutical Technology
- Process Development
- Manufacturing Science
- Technology Transfer
- Clinical Trial Material (CTM)
- #J-18808-Ljbffr
CMC Lead Formulation (w/m/d) in München Arbeitgeber: Progressive
Als Arbeitgeber in einem international führenden Biopharma-CDMO-Umfeld bieten wir Ihnen die Möglichkeit, aktiv an der Gestaltung von Qualitätsstrategien mitzuwirken und einen direkten Beitrag zur Versorgung von Patient:innen mit innovativen Biologika zu leisten. Unsere offene und partnerschaftliche Unternehmenskultur fördert die persönliche und berufliche Entwicklung, während modernste Produktionsplattformen und ein starkes Team von Experten Ihnen die Chance geben, Ihre Fähigkeiten in einem dynamischen Umfeld weiter auszubauen.
