- Novo Nordisk (Bloomington, IN)
- …+ Demonstrates understanding of the work tasks assigned + Executes complex with high quality + Knowledge of cGMP, ICH, FDA , EMA regulations or guidelines + ... life-changing careers, and the opportunity to help improve the quality of life for millions of people around the...of improvements + Ownership of Corrective Actions, Change Management, GMP document revision, review and approval + Participate and… more
- Novo Nordisk (Bloomington, IN)
- …area + Reviews and approves GMP documentations while ensuring safety and GMP quality compliance + Supports and leads continuous improvement projects + Hires, ... to embark on the opportunity to help improve the quality of life for millions of people around the...years relevant experience required + Leadership experience preferred + GMP experience preferred + Technical Requirements: + Excellent written… more
- Novo Nordisk (Bloomington, IN)
- …area + Reviews and approves GMP documentation while ensuring safety and GMP quality compliance + Supports and leads continuous improvement projects + Hires, ... to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana… more
- Novo Nordisk (Bloomington, IN)
- …area + Reviews and approves GMP documentations while ensuring safety and GMP quality compliance + Supports and leads continuous improvement projects + Hires, ... to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana… more
- Novo Nordisk (Bloomington, IN)
- …area + Reviews and approves GMP documentations while ensuring safety and GMP quality compliance + Supports and leads continuous improvement projects + Hires, ... our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. As a part of Novo… more
- Novo Nordisk (Bloomington, IN)
- …area . Reviews and approves GMP documentations while ensuring safety and GMP quality compliance . Supports and leads continuous improvement projects . Hires, ... to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana… more
- Lilly (Plainfield, IN)
- …Planning) + Financial planning and cost control + Replenishment and inventory strategy + GMP and regulatory compliance ( FDA , EU, etc.) + Third-party supplier and ... + **Cross-functional Teamwork:** Work closely with teams across Customer Service, Quality , Tech@Lilly, HR, and Finance to align logistics operations with broader… more
- Novo Nordisk (Bloomington, IN)
- …Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana site ... and/or Engineers + Strong understanding of guidance documents from FDA , EMA, PDA, ISPE, ASME, ISO, and other industry...observations, and completing corrective actions + Serves as a quality contact and subject matter expert (SME) for simple… more
- Novo Nordisk (Bloomington, IN)
- …+ Demonstrates understanding of the work tasks assigned + Executes complex with high quality + Knowledge of cGMP, ICH, FDA , EMA regulations or guidelines + ... to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana… more
- Lilly (Indianapolis, IN)
- …disciplines to support the TS /MS technical agenda, IAPI Business Plan priorities and GMP Quality Plan objectives. This person will work closely with the site ... at the site to ensure the highest standards of quality are being met through best-in-class processes, equipment, and...+ Key position responsibility is to address and document GMP compliance issues and development /execution of process /cleaning… more