Technician - QC Laboratory

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. 

Patients are at the center of everything we do at Lilly. We are currently hiring a Technician - QC Laboratory.

This role supports critical work that helps bring medicines and solutions to patients responsibly and efficiently. #WeAreLilly

QC Analyst – Finished Product (Scope):

Perform chemical testing and analysis on finished pharmaceutical products from manufacturing dry product, stability, and in-process (cleaning valuations) for quality control areas. Execute analytical methods in strict adherence to SOPs, pharmacopeial standards (USP/EP/BP), and GMP requirements. Verify data integrity of laboratory samples, support method validation activities, equipment qualification, and analytical method transfers to ensure product safety, efficacy, and regulatory compliance.

Education & Experience

• Bachelor’s degree in chemistry, or related natural science
• Minimum 1 years of relevant pharmaceutical or quality control laboratory experience
  • Experience with finished dosage form testing and/or pharmaceutical product analysis is strongly preferred
  • Experience in a GMP-regulated environment preferred

Technical Competencies

• Proficiency with analytical instrumentation – including but not limited to:
  • Chromatography techniques: HPLC, UPLC, or GC
  • Spectroscopy: UV-Vis, FTIR or NIR
  • Physical testing equipment: Analytical balances, microbalances, dissolution apparatus
  • TOC (Total Organic Carbon) analyzers
  • Familiarity with additional instruments (e.g., Karl Fischer titration, particle size analysis)

• Strong understanding of laboratory analysis best practices including:
  • Wet chemistry and quantitative analysis techniques
  • Proper sample preparation and handling procedures
  • Method validation principles and execution (ICH guidelines)
  • Data integrity and regulatory compliance (21 CFR Part 11, ALCOA+ principles)

• Demonstrated knowledge of pharmaceutical regulations and standards:
  • FDA regulations (21 CFR Parts 210-211, GMP requirements)
  • Pharmacopeial standards (USP, EP, or BP)
  • ICH Quality Guidelines

Laboratory & Soft Skills

• Strong analytical thinking and attention to detail with ability to troubleshoot analytical problems
• Proficiency in laboratory information management systems (LIMS) – or demonstrated ability to quickly learn proprietary systems
• Excellent written and verbal communication skills – able to clearly document results and present findings
• Ability to work independently and as part of a cross-functional team
• Commitment to quality and GMP compliance mindset

Language & Communication

• Bilingual proficiency in English and Spanish – written and verbal
  • Preferred for technical documentation, safety communications, and team collaboration in bilingual environments

Professional & Personal Attributes

• Problem-solving skills with ability to conduct root cause analysis and implement corrective actions
• Experience with method validation or analytical method transfer projects.
• Familiarity with statistical analysis tools or software (Empower, or equivalent)
• Certified Quality Analyst (CQA) or pursuit of analytical chemistry certification
• Flexibility and willingness to provide technical support to operations 24/7 as needed
• Ability to manage multiple priorities in a fast-paced, regulated environment while maintaining accuracy
• Demonstrated experience with process improvement or continuous quality initiatives
• Knowledge of automation tools or robotics in laboratory settings

• Experience with laboratory safety and environmental compliance programs
• Familiarity with Good Laboratory Practice (GLP) standards
• Background in stability testing protocols and long-term storage studies
• Experience with regulatory inspections, audit preparation, or quality investigations