Lilly

healthcare

AssociateDirector-TS/MS

$123–180k Indianapolis, Indiana, United States FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Associate Director - TS/MS at Lilly. Skills: process management, cross-functional coordination, vendor/stakeholder management. Oversee Commercialization mission for IDAP site. Lead/mentor technical staff”

What You'll Achieve.

Deliver on functional technical objectives; Deliver on specific product business plan; Deliver on quality objectives; Ensure Commercial Launch activities align with Site manufacturing goals; Deliver operational results for Clinical Trials and Commercial Launch

Industry & Context.

healthcare
Eligibility Requirements

Ability to wear safety equipment, Some allergens are present in the plant, Some travel may be required (<5%)

What They're Looking For.

Must Have

Bachelor's degree in Science or Engineering or equivalent experience, At least 5 years of pharma experience, Previous demonstration of leadership skills, Qualified applicants must be authorized to work in the United States on a full-time basis

Nice to Have

interpersonal and communication skills, Understanding of statistical process control and Six Sigma concepts, Solid understanding of quality and corporate policies, Solid understanding of the importance of and basic requirements of Regulatory agencies such as the FDA, EMA, OSHA, and EPA, Comprehension of MSOE’s, Demonstration of solid judgment and initiative, Responsible for maintaining a safe work environment, working safely, and accountable for supporting all HSE Corporate and Site Goals, Device assembly and / or packaging experience, Previous supervisory experience

What You'll Do.

Oversee Commercialization mission for IDAP site

Lead/mentor technical staff

Develop and implement technology transfer agenda

implement site business and Quality Systems

Influence commercial technical agenda

Address and document GMP compliance issues

Develop and execute validation plans

How You'll Work.

Team & Collaboration

Work with peer leadership; Encourage knowledge sharing and education within team; Collaborate with key internal partners: Operations, Quality Assurance, Quality Control Labs, Logistics, Engineering and Site Technology Transfer Team; Alignment of all functional Technical Services, Engineering, Utilities, Quality and Operations leadership; Represent their team on the plant flow teams

Full Job Description

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 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. **Position Brand Description:** The Associate Director TS/MS in Indianapolis Device Assembly & Packaging Operations is responsible for overseeing the Commercialization mission for the IDAP site per Manufacturing Standard for Operational Excellence (MSOE) 201. In addition, this position is responsible for leading/mentoring a technical staff and understanding device assembly, dry packaging and parenteral packaging processes. This includes responsibility for developing and implementing the organization’s technology transfer agenda, coordination, integration, replication and implementation of IDAP Site business and Quality Systems for the Commercial Launch activities. Influence and implement the commercial 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 position responsibility is to address and document GMP compliance issues and development/execution of validation plans. **Key Objectives / Deliverables:** * Technical and defendable process support service * Performance management and development of staff * Technical review and approval for site quality documents, plans, validation-related documents and studies. * Effectively encourage knowledge sharing and education within team and with key internal partners: Operations, Quality Assurance, Quality Control Labs,

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