Associate Director, TS/MS Manufacturing CMC Project Management

Lilly • Indianapolis, IN

8d • $117,000 - $171,600

About The Position

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 a 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.

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 management experience
• Demonstrated knowledge of CM&C aspects of Commercialization and Commercial Manufacturing
• Strong interpersonal and teamwork skills
• Strong oral and written communication skills
• Strong problem-solving skills, self-management and organizational skills.
• BSc or MSc in Chemistry, Biology, Engineering or equivalent Scientific degree.

Nice To Haves

• Demonstrated knowledge of CM&C aspects of Pharmaceutical Drug Development
• Experience in Technical Services/Manufacturing Services, Manufacturing Operations, and/or QA/QC within Pharmaceutical Manufacturing highly desirable.
• Experience with Smartsheet as a Project Management tool.
• Master’s in project management, PMP Certification, or MBA preferred.

Responsibilities

• 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.
• 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.
• 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.
• Mentorship of peers and team members
• Support process improvement
• Subject Matter Expert of a process or system

Benefits

• 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).

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level