Job Description
We are seeking a skilled professional to support our organization's mission of making a positive impact on people's lives. The ideal candidate will have expertise in manufacturing science and documentation requirements.
The successful candidate will be responsible for supporting site startup within the TSMS process through documentation preparation and review, monitoring processes during start-up/validation and ongoing manufacture, and establishing strong deviation investigation support and technical writing capabilities.
Key Responsibilities:
* Support process teams with documentation preparation, review, and approval
* Understand electronic batch records, process flow documents, and validation processes
* Engage regularly with molecule stewards to ensure accurate TSMS documentation
* Conduct root cause analysis to lead troubleshooting efforts
Required Skills and Qualifications
To succeed in this role, you will need:
* A Bachelor's or Master's degree in Chemistry, Biochemistry, or a related field
* 3-5 years of experience in pharmaceutical manufacturing
* Excellent verbal and written communication skills
* Strong analytical and problem-solving skills
* Collaborative skills with operations, process engineering, QCL, and other process team members
Benefits
We offer a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k), pension, vacation benefits, medical, dental, vision, and prescription drug benefits, flexible benefits, life insurance, and death benefits.
Others
This is a full-time equivalent position that may require travel to current startup sites and potential short-term assignments across the network. Lilly is an equal opportunity employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.