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).
Willingness to travel domestically and internationally to external manufacturing sites as required.
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 or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
