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Lilly Associate Director - Technical Services/Manufacturing Science Parenteral Manufacturing in Indianapolis, Indiana

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Job Description

Leading/mentoring a technical staff and understanding parenteral aseptic processing as it relates to drug product manufacturing. Provide guidance on time management and priorities for direct reports. Manage routine production support activities while balancing implementation of technical projects and process optimizations. The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards that support parenteral drug product manufacturing. Influence and implement the technical agenda within a multi-discipline technical environment. Work with peer leadership in a positive fashion to deliver on functional technical objectives, specific product business plan, and quality objectives.

Key Objectives/Deliverables:

Technical and defendable process support service

Performance management and development of staff

Partner within TS/MS and across functional disciplines to influence and implement the technical agenda, site business plan objectives and GMP Quality Plan objectives.

Technical review and approval for site technical and quality related documents and studies.

Basic Qualifications

Bachelor's Degree in STEM discipline

Additional Preferences:

Additional relevant industrial experience (greater than 5 years) in any of the following associated disciplines such as Technical Sciences, Manufacturing, Quality Control, Quality Assurance or Engineering.

Demonstrated leadership/administration.

Parenteral manufacturing experience.

Teamwork and interpersonal skills

Technical leadership, administrative and organizational skills

Problem solving and independent decision making skills

Multi-tasking and communications skills

Ability to influence diverse groups

Computer and statistical analysis skills

Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.

Other Information:

8 hour days –Monday through Friday

Applicant will work in various areas within the Parenteral Plant. Some allergens are present in the parenteral plant. Mobility requirements and exposure to allergens should be considered when applying for this position.

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As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law).