Associate Director, TS​/MS Manufacturing CMC Project Management

Location: Indianapolis

Associate Director, TS/MS Manufacturing CMC Project Management page is loaded## Associate Director, TS/MS Manufacturing CMC Project Management locations:
US, Indianapolis INtime type:
Full time posted on:
Posted Todayjob requisition :
R-101332

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:

** This role is responsible for integrating Manufacturing CMC elements to support molecule commercialization and to manage the development and implementation of an integrated technical plan for commercially manufactured molecules.  This position leads a cross functional team to ensure integrated and innovative CMC plans which accelerate life changing medicines to patients throughout the Manufacturing Life Cycle with safety first and quality always.  

The role is also responsible for coordinating the Global Product Assessment (GPA) for the molecule(s) 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
** Team Leadership
* Responsible for leading a Development and Manufacturing (central and site) team of moderate to high complexity and scope through development and execution of project plans that deliver strategic and operational objectives.
* Support the Development 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.
* Influence Development Manufacturing Technical Agenda and pre submission deliverables to enable effective transition to downstream Manufacturing plan/deliverables.
* Develop and manage an integrated Post Launch Technical Agenda for assigned molecules to support launch/commercial needs, reliable supply and productivity objectives.
* Responsible for the integration of the team plan to achieve Life Cycle Management objectives.

Project Management Leadership
* Responsible for delivery of project milestones on time and within scope through the utilization of project management approaches and tools.
* Document key team information and decisions and ensure project management systems are up to date.
* Encourage appropriate risk taking within the team by leading risk assessments and contingency planning at the team level.
* Resolve team issues with Manufacturing priorities in mind.
* Ensure strategic alignment with key stakeholders.
* Support upward and cross-functional communications.
* Actively track leading indicators of teams’ progress to major milestones.
* Build and maintain effective teams: motivate, recognize, coach & mentor team members and associates.
* Gain and share learning and optimized practices within and across teams.

Governance Facilitation and Reporting
* Responsible for facilitating Manufacturing Reviews and other governance alignment
* Ensure reporting of project status, metrics, and risk.  Escalate as necessary.
* Coordinate Global Product Assessments (GPAs), with Technical Stewards and Manufacturing sites, to ensure holistic review of control and capability of the manufacturing processes.

Functional Leadership
* Mentorship of peers and team members
* Support process improvement
* Subject Matter Expert of a process or system
** Basic Requirements:
*** Minimum 5 to 10 years’ experience in more than one Pharmaceutical Development CM&C function OR Pharmaceutical Manufacturing function/site
* Demonstrated leadership of cross-functional teams
* Demonstrated project…