The Quality Director, Quality Assurance and Analytical Service Operations will provide strategic, managerial, and technical leadership to both quality assurance and analytical development/QC teams.
This role is responsible for building, mentoring, and leading a high-performing team of scientists and quality professionals, fostering a collaborative and innovative work culture that aligns with site business objectives and to deliver first class services to customers.
- Strategic Leadership & Project Management:
- Develop and execute the overall QA strategy aligned with company goals and site business needs.
- Develop and implement phase-appropriate, modality (mostly small molecules and functional polymers) specific quality guidelines and analytical/QC strategies across numerous client projects, ensuring alignment with project timelines, budgets, and specific client requirements.
- Client & Business Development Support:
- Represent senior site leadership serving as the primary quality and analytical technical lead for clients, ensuring seamless communication and alignment of project goals.
- Collaborate with the business development team to evaluate and assess new client projects, contributing to proposals and technical discussions to secure new business.
- Ensure all quality operations and procedures adhere to global health authorities’ regulations and standards (ICH, FDA, EMA, cGMP/GLP) and corporate guidelines.
- Represent site and serve as a subject matter expert (SME) during client audits and health authority inspections.
- Team Management & Development:
- Lead, mentor, and build a high-performing, multi-function team of scientists and quality professional, fostering a collaborative and innovative work culture focused on client success and scientific excellence.
- Operational Excellence - quality:
- Establish and continuously improve the Quality Management System (QMS).
- Identify quality risks and implement mitigation strategies.
- Oversee batch record/data review and production releases based on defined criteria.
- Drive root-cause analysis (RCA) and corrective/preventive actions (CAPA).
- Operation Excellence - analytical development and QC:
- Oversee the development, transferring, qualification, and validation of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, IC, and GPC-MALS, etc.) for release, stability, and characterization testing for drug substances and functional excipients.
- Providing expert scientific guidance in troubleshooting & investigations.
- Operation Excellence - technology:
- Strategic planning and forecasting on capital investment in quality and analytical technologies aligns with business growth.
- Implement and enforce industry best practices and drive adoption of modern tools and frameworks in analytical development/QC fields.