Associate - Qa API Em

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN

This role provides quality oversight of Quality Control activities at Contract Manufacturing organizations (CMs) for Active Pharmaceutical Ingredients (API) External Manufacturing. It involves ensuring compliance with cGMPs, supporting method validation/transfer, and managing quality-related issues with testing.

What you'd actually do

  1. Provide quality oversight of Quality control activities at CMs including being the initial point of contact for all quality-related issues with testing.
  2. Provide quality oversight of CM method validation or method transfer activities
  3. Coordinate and perform quality responsibilities of API shipments for stability testing. Provide quality oversight of API EM stability program.
  4. Ensure that documented checks have been completed for the Certificates of Testing and Certificates of Environmental Monitoring (where applicable), and deviations, changes and batch documentation that demonstrates requirements have been met prior to batch release.
  5. Provide quality support of Quality Control with the focus on holistic review of key activities associated with or impacting the quality control testing including deviations, change controls and countermeasures.

Skills

Required

  • BS in a science-related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences
  • 5+ years of GMP Quality Control Laboratory knowledge and/or experience in API or finished product manufacturing, QA or Engineering
  • Authorized to work in the United States on a full-time basis

Nice to have

  • Testing experience with Small Molecule
  • Thorough technical understanding of quality systems and regulatory requirements relating to quality control laboratories
  • Knowledge of pharmaceutical manufacturing operations
  • Demonstrated coaching and mentoring skills
  • Experience in root cause analysis
  • Demonstrated application of statistical skills
  • Demonstrated strong written and verbal communications skills
  • Strong attention to detail
  • Proficiency with computer system applications
  • Excellent interpersonal skills and networking skills
  • Ability to organize and prioritize multiple tasks
  • Ability to influence diverse groups and manage relationships

What the JD emphasized

  • 5+ years of GMP Quality Control Laboratory knowledge and/or experience in API or finished product manufacturing, QA or Engineering.
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization and visas for this role