Associate Director, Product Quality

🕒 il y a 15 jours

🇺🇸 États-Unis – Télétravail

💵 $117 000 - $189 200 / an

⏰ Temps Plein

🟠 Senior

👔 Directeur

🗣️🇺🇸🇬🇧 Anglais requis

D'où vient cette offre

Publiée sur la page carrières de Eli Lilly and Company, pas via un site d'emploi

Repérée par Remote Rocketship il y a 15 jours

Toujours ouverte sur le site de Eli Lilly and Company. Vérifiée il y a 2 heures.

Logo of Eli Lilly and Company

Eli Lilly and Company

10 000+ employés

💊 Pharmaceutique

🏥 Santé

🧬 Biotechnologie

💰 €6 500 000 Post-IPO Debt - Eli Lilly en 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company est une entreprise pharmaceutique multinationale qui recherche, développe, fabrique et commercialise des médicaments sur ordonnance dans plusieurs domaines thérapeutiques, y compris le diabète, l'oncologie, l'immunologie, les neurosciences et la douleur. Basée à Indianapolis, dans l'Indiana, Lilly est reconnue pour sa vaste R&D, le développement clinique et la commercialisation mondiale de médicaments biologiques et de petites molécules. L'entreprise se concentre sur la découverte de médicaments, les essais cliniques, les approbations réglementaires et la fabrication et distribution pharmaceutique à grande échelle.

Description

• Design, implement, and scale a Quality Management System appropriate to the company’s stage of development and product pipeline • Provide GxP compliance oversight for internal functions and outsourced partners, including CDMOs, CROs, and testing labs • Ensure robust supplier management and audit programs • Lead Quality function activities, including deviations, CAPAs, change control, document control, and training • Serve as quality lead for regulatory submissions, including INDs, CTAs, and NDAs, clinical trial material release, and validation programs • Drive quality input for tech transfers, CMC activities, and scale-up plans • Oversee batch record review, product release, and Quality review of analytical and manufacturing documentation • Prepare the company for regulatory inspections and third-party audits • Serve as a primary quality representative to health authorities • Hire, mentor, and lead a small team of QA professionals • Foster cross-functional communication and a culture of accountability • Perform other responsibilities as assigned • Help build and lead the quality function supporting compliance with GxP regulations and product development and commercialization goals

🎯 Exigences

• BS or higher in Life Sciences, Chemistry, Pharmacy, or related field • 8+ years of experience in pharmaceutical quality roles, including 3+ years in a leadership position • Experience with document control software, such as ZenQMS, Veeva Vault, or MasterControl • Strong knowledge of GxP regulations, including FDA, EMA, and ICH, and quality best practices across the product lifecycle • Familiarity with multiple dosage forms and CDMO-based manufacturing • Proven ability to operate effectively in a resource-constrained, fast-paced setting • Excellent leadership, communication, and cross-functional collaboration skills • Ability to balance compliance rigor with operational efficiency • Prior involvement in successful regulatory submissions and inspections is a plus • Early-stage development or startup experience preferred

🏖️ Avantages

• Company bonus depending, in part, on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical, dental, vision and prescription drug benefits • Flexible benefits, including healthcare and/or dependent day care flexible spending accounts • Life insurance and death benefits • Certain time off and leave of absence benefits • Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities • Occasional travel up to 20%

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