Principal - Qa API External Manufacturing Peptides

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN +1

This role provides Quality Assurance oversight for API External Manufacturing operations, ensuring compliance with cGMP and regulatory requirements for products manufactured by third-party partners. Responsibilities include leading quality aspects of external sites, conducting audits, reviewing documents, collaborating cross-functionally, providing QA guidance, developing quality agreements, investigating incidents, and representing Lilly during regulatory inspections.

What you'd actually do

  1. Lead and manage quality aspects of external API manufacturing sites, including but not limited to batch record review, disposition, deviation management, and change control.
  2. Conduct and/or participate in quality audits of external manufacturing sites to assess compliance with cGMP, regulatory expectations, and Eli Lilly's quality standards.
  3. Review and approve quality-related documents, such as manufacturing master batch records, validation protocols and reports, stability data, and analytical methods.
  4. Collaborate cross-functionally with internal teams (e.g., Supply Chain, Regulatory Affairs, Technical Services) and external manufacturing partners to resolve quality issues and drive continuous improvement.
  5. Provide expert QA guidance and support during new product introductions and technology transfers to external manufacturers.

Skills

Required

  • Bachelor's degree in Chemistry, Biochemistry, Pharmacy, Chemical Engineering or related scientific discipline.
  • Minimum 5 years experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry, with a strong focus on API manufacturing and external supply.
  • Experience in cGMP regulations (FDA, EMA, HPRA, etc.) and global pharmacopeial requirements.
  • Experience in auditing external manufacturing sites.
  • Experience in quality management systems (e.g., Veeva).

Nice to have

  • Strong understanding of API manufacturing processes, analytical techniques, and quality control principles.
  • Demonstrated ability to make sound quality decisions and effectively communicate complex technical and quality information to diverse audiences.
  • Excellent problem-solving, analytical, and critical thinking skills.
  • Ability to work independently and as part of a team in a fast-paced, dynamic environment.

What the JD emphasized

  • cGMP regulations
  • audits of external manufacturing sites
  • quality agreements