Associate Director
2 weeks ago
Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world. Our employees work together to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We're looking for individuals who are determined to make a positive impact on people's lives.
Purpose:
The Associate Director, Medicines Quality Organization (MQO) - Safety role is responsible for leading quality system compliance and quality improvement of the functions they support. This includes managing the quality team, developing and implementing quality plans, and ensuring compliance with regulatory requirements. The Associate Director is also responsible for audit and inspection support, quality project management, and process improvements.
Primary Responsibilities:
This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.
- Leadership and Supervision
- Quality System Implementation
- Audits and Inspections
- Project Management and Process Improvement
Minimum Qualification Requirements:
• Bachelor's Degree, preferably in a health-related or scientific field
• Three to five years' experience in quality and/or patient safety
Other Information/Additional Preferences:
• Health care professional
• Supervisory experience
• Strong leadership and self-management skills, including the ability to manage initiatives simultaneously
• Ability to communicate effectively, both written and verbal
• Application of risk-based decision making in a regulated environment
• Ability to influence, challenge, and work in cross-functional teams and at different levels
• Excellent interpersonal, organizational, and negotiation skills
• Strong knowledge of quality systems and/or experience in a quality control/quality assurance role
• Knowledge of pharmacovigilance regulations/guidelines
• Project management experience/skills
• Demonstrated ability to work in a global environment
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups.
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