Drug Substance Manager*

AiCuris GmbH; Wuppertal; Hybrid; EUR 80.000 - 120.000; Vollzeit

Zusammenfassung

Eine innovative Pharmafirma in Wuppertal sucht einen Drug Substance Manager zur Unterstützung in der CMC-Entwicklung. Der Bewerber sollte über einen PhD in Chemie oder verwandten Bereichen verfügen und umfassende Erfahrung in der Verwaltung von CMO/CDMO sowie in der CMC-Entwicklung mitbringen. Die Position erfordert exzellente organisatorische und kommunikative Fähigkeiten sowie die Fähigkeit, mehrere Projekte gleichzeitig zu verwalten. Flexible Arbeitszeitmodelle und ein attraktives Leistungspaket werden geboten.

Leistungen

Arbeitgeberfinanzierte Altersvorsorge

Attraktives Leistungspaket

Entwicklungsmöglichkeiten

Flexibles Arbeiten

Qualifikationen

• Mindestens 5 Jahre Berufserfahrung in der Pharma- oder Biotech-Branche.
• Erfahrung in der CMC-Entwicklung für frühe und späte Programme.
• Vertrautheit mit GMP-konformer Herstellung und Testung.

Aufgaben

• Verwaltung von CMO/CDMO/CRO in der API-Herstellung.
• Enge Zusammenarbeit mit QA/QC.
• Unterstützung bei regulatorischen Einreichungen in den USA und der EU.

Kenntnisse

Analytische Fähigkeiten

Projektmanagement

Kommunikationsfähigkeiten

Teamarbeit

Eigenverantwortung

Ausbildung

PhD in Chemie oder pharmazeutischer Technologie

Jobbeschreibung

Your mission

As a Drug Substance Manager* you will be part of our CMC management team supporting all development projects with respect to managing clinical and commercial drug supply, ensuring product quality, managing CMOs/ CDMOs/ CROs, and preparing CMC documentation for regulatory dossiers.

Responsibilities

• CMO/ CDMO/ CRO management for API manufacturing of small molecules and Tides (mainly Oligonucleotides) for clinical study supply and early commercial phases
• Management of all aspects of technical drug substance development (eg, analytics, solid state assessment, impurity profiling, route finding)
• Close interaction with QA/QC to manage CAPAs, change controls, quality incidents, writing of SOPs and participating in audits as technical expert
• Supply chain management of APIs, Regulatory Starting Materials, and other critical reagents
• Support of selection and evaluation of suitable CMOs/ CDMOs/ CROs for GMP manufacture and testing
• Cost of good assessment, support of commercial phase preparation, and post-approval activities
• Support of regulatory fillings in US and EU (eg, CTD module 3) and review of quality documentation relevant for manufacturing and testing (eg, MBR, validation protocols)

Your profile

• PhD (or equivalent) in Chemistry or Pharmaceutical Technology or similar
• At least 5 years of post-graduate professional experience in the pharmaceutical / biotech industry
• Profound experience in CMC development for early- and late-phase programs, specifically with drug substance related activities
• Exposure to the principles of QbD (Quality by Design) and DoE (Design of Experiment)
• Experience in CMO/CDMO/CRO management and collaboration with external partners
• Experience with supporting regulatory filings in US and EU
• Sound expertise in GMP-compliant drug substance manufacturing and testing, including validation and transfer
• Ability to efficiently evaluate, prioritize and handle multiple project tasks
• Highly motivated and ability to work independently as well as in the team
• Excellent organizational and communication skills
• Business fluent in English; German skills would be beneficial

Why us?

• Unique corporate culture:Scientific excellence, a collaborative working environment and the passion to improve the lives of patients defines our work. With us, you can work together with innovation awarded experts with the proven ability to translate science into commercial success. You can expect diversity, inspiration, as well as trustful collaboration.
• Development: We encourage people to grow and strongly support individual development and learning opportunities.
• Flexibility: Embracing flexible working accommodations, we enable our people to integrate business into their personal life.
• Benefits: Employer-funded pension comes along with an attractive benefits package