- Sumitomo Pharma (Indianapolis, IN)
- ** Associate Director , GMP Quality Control** Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical ... seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of… more
- Lilly (Lebanon, IN)
- …into GMP manufacturing operations._ **Main Purpose and Objectives of Position:** The Associate Director Health, Safety, and Environmental (HSE) serves as the ... tank farms, utilities, waste operations, and laboratory and administrative facilities. The Associate Director HSE is responsible for the productivity and… more
- Lilly (Indianapolis, IN)
- …may impact a positive benefit-risk balance for a given product. The Associate Director Pharmacoepidemiology Study Operations (AD Ops)is responsible for providing ... processes for completing this work and other related PE project work. The primary purpose of the AD Ops...as appropriate. + Establish regular communication with key GPS, regulatory , business unit (BU) and affiliate personnel as appropriate… more
- Lilly (Lebanon, IN)
- …a successful startup into GMP manufacturing operations._ **Position Description:** The Associate Director - Technical Services/Manufacturing Science (TSMS) is ... responsible for managing the activities of TSMS personnel. The Associate Director TSMS must balance coaching a technical staff, prioritization and staffing for… more
- Lilly (Lebanon, IN)
- …a successful startup into GMP manufacturing operations. **Position Description:** The Associate Director Engineering - Utilities provides leadership and ... engineering team responsible for plant and environmental control utilities. The Associate Director Engineering Utilities ensures that engineering deliverables… more
- Lilly (Indianapolis, IN)
- …twins, computational modeling, edge/IoT, and analytics solutions. **Responsibilities:** The Associate Director - Digital Manufacturing Engineering position has ... prioritizing work, and supporting the overall DME strategy. The Associate Director role will provide discipline leadership...verbal and written communications skills + Experience in Capital project delivery + cGMP Regulatory knowledge in… more
- Wolters Kluwer (Indianapolis, IN)
- …here. (https://youtu.be/OZ2kSzAaXK4?si=sDgZ7DZUbMnBddMq)** **What We Offer: ** The Market Research Associate Director role offers growth potential opportunities, ... the way we do business, build better judicial and regulatory systems. We help them get it right. **Who...benefits. **What You'll be Doing:** As our Market Research Associate Director , you will share your in-depth… more
- Lilly (Lebanon, IN)
- …successful startup into GMP manufacturing operations._ **Position Description:** The Maintenance Associate Director provides leadership and direction to the ... and reliability groups within the site engineering organization. The Maintenance Associate Director ensures that maintenance and reliability deliverables are… more
- Lilly (Lebanon, IN)
- …a successful startup into GMP manufacturing operations._ **Position Brand Description:** The Associate Director for Tank Farm and Solvent Recovery Operations is ... and compliantly support the manufacturing of high-quality medicine. The Associate Director for Tank Farm and Solvent...a validated state for their respective area. In the project delivery phase and startup phase of the … more
- Lilly (Indianapolis, IN)
- …Lilly and Active Pharmaceutical Ingredient (API) Contract Manufacturer representatives. The JPT Associate Director is the key business relationship owner and is ... materials are delivered on time and within downstream customer expectations. The JPT Associate Director will partner with Lilly's Process Research & Development… more
- Lilly (IN)
- …California; South San Francisco, California; Stamford, Connecticut; and Madrid, Spain. The Associate Director , Medical Writing will be responsible for the ... writing deliverables that support the clinical development, safety, and regulatory requirements of a clinical program. **Responsibilities:** + In collaboration… more
- Merck (Indianapolis, IN)
- …Pharmacology and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global Clinical ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- Lilly (Indianapolis, IN)
- …people who are determined to make life better for people around the world. The Associate Director - Quality Control is responsible for managing the activities of ... Quality Control personnel. The Assoc. Director Quality Control must balance coaching a technical staff, prioritization and staffing for routine production support… more
- Lilly (Indianapolis, IN)
- …a wholly owned subsidiary of Eli Lilly and Company. **Position Summary:** The Associate Director of Quality Engineering and Computer System Validation (CSV) is ... to POINTs Engineering and Computer System Validation processes. The Associate Director of Engineering and CSV will...procedures and policies remain current to relevant company and regulatory requirements. + Assist in the design of validation… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. ** Associate Director ** **; CMC, Device Development Program Manager** **Functional Area: ... device team members, program teams and functional leads. + Provide CMC Project Management for both internal and external CMC development and manufacturing… more
- Lilly (Indianapolis, IN)
- …an operational rhythm, supplier performance and contract management. **Responsibilities:** The ** Associate Director - Global Materials Planning - Central Lead** ... + Define and implement a segment-based approach for critical materials and suppliers project to set the foundation of future operating models. + Collaborate with… more
- Merck (Indianapolis, IN)
- …teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing ... as well as preparing for, management and follow up of regulatory inspections. **Primary Responsibilities:** Operational Quality Management + Develop Risk Assessment… more
- Lilly (Indianapolis, IN)
- …to develop medicines with safety first and quality always. We are seeking an Associate Director -Learning and Development MQ IT Systems to join our Global ... curriculum architecture. + Define qualification programs based on business and regulatory requirements. + Prioritize and manage learning activities and requests… more
- Lilly (Indianapolis, IN)
- …deployment of machine learning models, adhering to ethical AI practices and regulatory requirements. How You Will Succeed: + Problem Solving with Advanced Analytics: ... methodologies to maintain competitive and technological edge. + Leadership in Project Execution: Drive projects from conception to completion, providing technical… more
- Lilly (Indianapolis, IN)
- …black belt with relevant experience 6. Commercial and financial awareness with Project management skills (PMP Certified preferred) 7. Familiarity with regulatory ... requirements and compliance in the pharmaceutical industry Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively "Lilly") are committed to help individuals with disabilities to participate in the workforce and ensure equal… more