Director, CMC – Formulations

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🕒 vor 28 Tagen

🏄 California – Remote

🏄 California – Remote

💵 $190.000 - $260.000 / Jahr

⏰ Vollzeit

🔴 Experte

👔 Direktor

Jetzt Bewerben

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Codera

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11 - 50 Mitarbeiter

🧬 Biotechnologie

💊 Pharmazie

🤝 B2B

Biotechnology • Pharmaceuticals • B2B

Codera ist ein B2B-Unternehmen, das mit Biotechnologie- und Pharmaunternehmen zusammenarbeitet, um umfassende Fachkenntnisse und Infrastruktur für die Arzneimittelentwicklung bereitzustellen. Es unterstützt Kunden im gesamten Lebenszyklus der Arzneimittelentwicklung mit technischen, betrieblichen und infrastrukturellen Dienstleistungen, um therapeutische Programme voranzutreiben.

Beschreibung

• Assist with the design and evaluation of drug product formulations, primarily small molecule formulations, to achieve specific pharmacokinetic (PK) goals • Contribute to CMC and development strategy • Manage relationships with various contract development and manufacturing organizations (CDMOs), analytical labs and contract research organizations (CROs) • Assist with the clinical supply logistics • Prepare, analyze and interpret analytical data that integrate into regulatory and intellectual property (IP) documents • Draft, edit and review sections of regulatory and IP documents • Provide scientific input for analytical protocols and study reports • Contribute to a fast-paced, dynamic, data-driven scientific culture that embraces innovation and excellence • Research CMC and formulation topics to support Tang Capital’s investments • Participate in business development activities, as requested

🎯 Anforderungen

• Bachelor’s degree or higher in life sciences or related discipline required • Master’s degree preferred • Minimum of 5 years in relevant pharmaceutical industry work experience required • Experience with small molecule formulations required • Experience with biologics formulations preferred • Experience working with CDMOs and analytical labs • Experience with one or more of the following drug product formulation strategies: modified/delayed release, fixed-dose combinations, spray-dried dispersions • Experience with a wide range of excipients and formulation technologies • Experience with formulations for oral, subcutaneous and/or inhaled delivery • Ability to research, synthesize and summarize complex CMC topics • Experience writing and/or reviewing regulatory documents, including Investigational New Drug (IND)/New Drug Application (NDA) sections • Ability to effectively organize and manage multiple assignments with challenging timelines from project start-up through submission • Excellent knowledge of Food and Drug Administration (FDA) and International Council for Harmonisation (ICH) regulations and Good Manufacturing Practices (GMP) • Outstanding written and verbal communication skills, including the ability to use clear language to explain complex ideas • Ability to establish and maintain collaborative working relationships with internal and external stakeholders.

🏖️ Vorteile

• employer sponsored insurance plans including medical, dental and vision coverage • generous paid time off • retirement plan options • additional wellness and professional development programs