Local / Onsite
Eli Lilly and Company has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines—investing a higher percentage of our sales in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in Class” Pharmaceutical company, please review the following opportunity.
THIS IS NOT A PERMANENT POSITION. FIXED DURATION OPPORTUNITY OF UP TO FOUR YEARS
Support the BR&D manufacturing operation, particularly as it relates to decisions associated with impact to the quality of products
Evaluate and determine the disposition of batches, including the GMP status and compliance to Regulatory commitments
Perform Regulatory re-releases
Perform pre- and post-approval of batch production records utilized for manufacturing
Maintain and analyze site quality metrics
Identify opportunities for and participate in continuous improvement
Ensure inspection readiness through compliance auditing, site self-assessments, GMP education, monitoring, establishing and enhancing Quality system
Previous work experience in a regulated environment
Qualified candidates must be legally authorized to be employed in the United States. Eli Lilly and Company does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Bachelors degree in a science field preferred
Work independently, pay attention to detail, and exhibit decision making and problem solving skills
Ability to prioritize and multi-task
Interpersonal skills, particularly working in a peer relationship with technical scientists and operations
ELI LILLY AND COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER
Eli Lilly - 21 months ago
Eli Lilly and Company discovers, develops, manufactures and sells products in one business segment, pharmaceutical products. The Company...