Eli Lilly and Company logo

Sr. Director - API Manufacturing Quality Control

Eli Lilly and Company
Full-time
On-site
Houston, TX
$151,500 - $222,200 USD yearly
Operations

Want to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now — JobsAI.

Role Summary

The Sr. Director – QC provides strategic and administrative leadership for the quality control and analytical sciences laboratories at a new Lilly API site. This role ensures the development of essential capabilities and business processes to support site operations and Lilly’s expanding pipeline.

Responsibilities

  • Build and lead a high-performing Quality Laboratory Operations team
  • Ensure GMP compliance across all lab activities
  • Deliver the “lab of the future” vision with integrated digital, paperless processes
  • Collaborate with local and global quality teams to standardize lab design, processes, and systems
  • Participate in site and quality leadership teams
  • Drive strategic decisions and successful business outcomes
  • Coordinate lab-related planning and budget management
  • Promote cross-functional integration and communication
  • Maintain a safe, compliant work environment
  • Serve as a liaison for corporate communications
  • Ensure consistent quality and compliance across laboratories
  • Manage regulatory and internal inspections
  • Lead HR planning, performance management, and talent development
  • Recruit and build site capabilities for a high-functioning QC lab organization
  • Ensure strong administrative and technical leadership within the team

Qualifications

  • Bachelor’s degree in relevant field (STEM preferred)
  • 10+ years of supporting complex analytical testing (mass spec, bioassay, protein characterization)
  • 5+ years of supervisory/leadership experience
  • Knowledge of QC operations, new product introduction, and process development (Preferred)
  • Expertise in analytical lab quality and compliance requirements (Preferred)
  • Experience with regulatory submissions (Preferred)
  • Proficient in Microsoft Office and other computer systems (Preferred)
  • Strong technical writing and communication skills (Preferred)
  • Effective interpersonal skills with ability to lead leaders and influence cross-functionally (Preferred)
  • Commitment to maintaining a safe work environment (Preferred)
Apply now
Share this job