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.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$114,000 - $167,200

For 140 years, Lilly has manufactured medicines that improve people’s lives around the world. We produce our medicines using some of the most sophisticated manufacturing technologies and rigorous quality standards. Lilly Manufacturing strives for excellence in its process, standards, procedures and behaviors to develop medicines with safety first and quality always.

Position Brand Description:

This role is responsible for managing the development and implementation of an integrated technical plan for commercially manufactured molecules.  The position must influence the organization around selection and investment for a specific product's/molecule’s Global Post-Launch Optimization Team (GPLOT).  The position is also responsible for coordinating the Global Product Assessment (GPA) for the product(s)/molecule(s) in which they support.  A person in this position would have a CM&C focus, be expected to apply Project Management principles, provide decision-making leadership for a cross functional team, and participate in process improvement activities within manufacturing. 

Key Objectives/Deliverables

Lead Global PLOT sub-teams of moderate to high complexity and scope through development and execution of project plans that lead to operational objectives.   

Develop and manage technical agendas for each molecule. 

Accountable for delivery of project milestones on time and within scope through utilization of project management standards. 

Coordinate GPAs with molecule stewards and manufacturing sites to ensure holistic review of control and capability of the manufacturing processes. 

Support the CM&C teams in developing strategies and implementing operational plans to deliver required materials (such as API, drug product formulations, registration stability lots, clinical trial materials, etc) as needed to support a particular project.   

Resolve issues with the cross-functional project team with TS/MS priorities in mind. 

Encourage appropriate risk taking within the team by leading risk assessments and contingency planning at the team level. 

Ensure strategic alignment with Business Unit and Manufacturing partners.  

Effectively manage upward and cross-functional communications. 

Understand the commercial needs/drivers for the technical projects and ensure that they are consistent with the overall technical agenda. 

Build and maintain effective teams: motivate, recognize, coach & mentor team members and associates. 

Gain and share learning and optimized practices within and across teams. 

Document key team information and decisions and ensure project management systems are up to date (MS Project,Smart Sheets , etc.). 

Identify and monitor critical path. 

Actively track leading indicators of teams’ progress to major milestones. 

Basic Requirements:

BSc or MSc in Chemistry, Biology, Engineering or technical related scientific degree

Minimum of 7 to 10 years experience in more than one CM&C function or manufacturing site, with site experience including site roles ideally within device assembly/packaging

Demonstrated leadership of cross-functional teams 

Demonstrated project management experience 

Demonstrated knowledge of CM&C aspects of drug development and manufacturing 

Additional Preferences:

Strong interpersonal and teamwork skillsStrong oral and written communication skills that demonstrate an ability to effectively (clearly, succinctly) communicate with all levels of the organizationStrong problem-solving skills, self-management, and organizational skillsExperience in Operations, TS/MS, QA or QC, Regulatory, or Supply Chain within pharmaceutical manufacturingGreen Belt or Black Belt experienceTechnical transfer experienceMasters in Project Management, PMP certification, PE or MBA

Other Information: Minimal travel (10%), domestic and international, may be required.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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