What You Will Do
Working within the Quality Operations structure, in a leadership capacity, you will be responsible for quality-related activities, including but not limited to:
1. Leading multiple high-performing quality teams across disciplines, providing technical guidance and fostering a proactive, continuous improvement environment.
2. Ensuring the organization’s conformance and commitment to meeting or exceeding customer requirements and regulatory standards.
3. Sponsoring a compliance environment by defining quality standards and roles/responsibilities with business partners.
4. Promoting a positive employee environment through open communication, engagement, and development, fostering trust, teamwork, and inclusiveness.
5. Managing talent selection, training, and performance management to develop future leaders and experts.
6. Maintaining certification compliance with regulatory bodies and engaging in audit programs such as Corporate, notified body, and FDA audits.
7. Controlling product/process deviations, implementing corrective actions, and managing product and patient risk.
8. Monitoring Quality KPIs, addressing trends and deviations, and participating in global improvement forums.
9. Developing a quality improvement pipeline aligned with global strategies to enhance product quality, resolve NCR & CAPA issues, reduce costs, and improve risk management.
10. Fostering global collaboration, aligning strategies with industry best practices, and benchmarking against regulatory requirements.
What You Will Need
* Bachelor’s Degree in Engineering, Science, or equivalent; Business Management or MBA is advantageous.
* Minimum of 10+ years experience in a regulated manufacturing environment such as Medical, Pharmaceutical, Bio-Medical, or Automotive.
* Minimum of 6+ years experience managing a talented, engaged, and high-performing team.
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