Site Compliance Leader

Eli Lilly Eli Lilly · Pharma · Houston, TX

The Site Compliance Leader at Eli Lilly is responsible for managing compliance to all regulatory requirements for next-generation biotech facilities. This role involves overseeing quality systems and processes, providing quality and technical expertise, and ensuring adherence to corporate quality standards and initiatives. The position requires extensive experience in quality assurance within the biotechnology or pharmaceutical manufacturing environment and a strong understanding of regulatory compliance.

What you'd actually do

  1. Ensure that processes needed for the Houston quality management system are established and documented.
  2. Monitor and report on the effectiveness of the quality management system and needed improvements.
  3. Ensure awareness of applicable regulatory requirements and quality management system requirements throughout the organization.
  4. Liaise with and influence central groups on corporate quality standards and initiatives.
  5. Sponsors site initiatives related to quality and compliance; supports network initiatives related to quality and compliance for local implementation; acts as connection for global initiatives related to quality and compliance for local implementation.

Skills

Required

  • BSc, Hons BSc, MSc, or PhD in Pharmacy, Science, Engineering, Quality, or related discipline.
  • Minimum of 12+ years of experience in quality assurance within a biotechnology or pharmaceutical manufacturing environment.
  • Demonstrated capability to effectively prioritize tasks and responsibilities
  • Ability to work independently
  • Excellent communication skills, both written and verbal, allowing for clear and concise expression of ideas, instructions, and feedback.
  • Effective decision-making
  • Exceptional ability to build and maintain positive relationships with colleagues, clients, and stakeholders
  • Fundamental knowledge of computer applications
  • Strong problem-solving skills
  • Experienced in creating clear and comprehensive procedures and training materials
  • Proven ability to mentor and lead others, providing guidance, support, and motivation to help them achieve their goals.
  • Strong follow-up skills, ensuring that tasks and projects are completed on time and to the required standard.

Nice to have

  • Proficient in English.

What the JD emphasized

  • regulatory requirements
  • quality management system
  • biotechnology or pharmaceutical manufacturing environment