All Of Our Groups
Healthcare
AssociateDirector–TS/MSCentralTeam
Neural analysis suggests this role is
optimal for Director candidates.
“Associate Director – TS/MS Central Team at All Of Our Groups. Skills: TS/MS support, Manufacturing, Quality assurance, Team leadership. Maintain a safe work environment. Lead safety initiatives”
Industry & Context.
Problem solving; Independent decision-making
Flexible in providing support, Occasional extended hour work, Occasional off-hour work
What They're Looking For.
Must Have
Bachelor's Degree in scientific disciplines, 5+ years pharmaceutical manufacturing experience, 3+ years experience leading teams, Authorized to work in the United States
Nice to Have
Technical aptitude, Ability to train and mentor, Proven Teamwork and interpersonal skills, Problem solving and independent decision-making skills, Oral and written communication skills, Ability to influence diverse groups, Experience with deviation and change management systems, Experience interacting with external vendors, Understanding of GMP supplier qualification processes
What You'll Do.
Maintain a safe work environment
Lead safety initiatives
Support HSE Corporate and Site Goals
Drive safety and quality culture
Understand scientific principles for manufacturing
Provide technical guidance
Understand manufacturing control strategy
Influence manufacturing control strategy
Drive control for the process
Drive capability for the process
Drive productivity for the process
Drive continuous improvement for the process
Review GMP documentation
Approve GMP documentation
Work cross-functionally with process teams
Provide oversight for supplier interactions
Engage with Procurement and Materials Management QA
Support GMP supplier qualification activities
Influence the technical agenda
Implement the technical agenda
Influence site business plan objectives
Implement site business plan objectives
Influence GMP Quality Plan objectives
Implement GMP Quality Plan objectives
Network with global parenteral sites
Collaborate with global parenteral sites
Understand best practices
Participate in tactical business planning
Participate in strategic business planning
Support site inspection readiness
Support site inspection execution
Interact with Regulatory Agencies
Performance management of staff
How You'll Work.
Team & Collaboration
Cross-functional teams; Global parenteral sites; Procurement and Materials Management QA
Communication Scope
Oral communication; Written communication
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. **Organization Overview:** The IPM TS/MS Central Team is a new team provides centralized TS/MS support for both the Insulin and Syringe Plants. This group will own Components, Materials, Annual Product Review, and Visual Inspection Qualifications. **Responsibilities:** The Associate Director, TS/MS Central Team role will report directly to the IPM TS/MS Associate Vice President and will be responsible for leading and mentoring the technical staff. * Responsible for maintaining a safe work environment, leading safety initiatives, and working safely and accountable for supporting all HSE Corporate and Site Goals. * Drive safety and quality culture within the organization * Understand the scientific principles required for manufacturing products in area of influence including the interaction of the chemistry, equipment, materials, aseptic processes, and container closure systems. * Provide technical guidance to the TS/MS group. * Understand and influence the manufacturing control strategy for the various operational areas. * Drive control, capability, productivity, and continuous improvement for the process. * Review and approve GMP documentation including procedures, deviation investigations, technical reports, change controls, regulatory submissions, APRs, etc. Work cross-functionally with the area process teams for metrics reviews, operational support, and issue / deviation management. * Provide oversight for interactions with
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