- 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 ... equipment and associated production systems operate in a safe, and quality -oriented manner. Responsibilities include: providing training and assessment support for… more
- Lilly (Indianapolis, IN)
- …pharmaceutical manufacturing processes and compliance with industry-specific regulations, such as FDA guidelines for Good Manufacturing Practices ( GMP ). + ... Doing** : You will be part of Tech@Lilly MQ (Manufacturing and Quality ) an organization that drives manufacturing operational excellence through utilization of… more
- Cardinal Health (Indianapolis, IN)
- …and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment._ ... sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (ie FDA , NRC, DOT) to support patient treatment through disease diagnosis,… more
- BioLife Plasma Services (Indianapolis, IN)
- …tasks require prolonged glove wear **PREFERRED QUALIFICATIONS:** + Experience working with SOPs, GDP, GMP , CLIA, and the FDA + Experience working in a highly ... your skills by contributing to financial, marketing, administrative, regulatory, quality , people, and facilities management. + **Contribute to Creating Life-Changing… more
- BioLife Plasma Services (Indianapolis, IN)
- …tasks require prolonged glove wear **Preferred Qualifications** + Familiarity with SOPs, GDP, GMP , CLIA, and FDA regulations + Experience working in a regulated ... experience in operational production, including financial, regulatory, administrative, marketing, quality , facilities, and people management. Gain exposure to real-world… more
- Lilly (Indianapolis, IN)
- …documented processes and procedures are in place for all activities to meet quality and compliance standards. + Must develop a deep understanding of the ... global serialization strategy for packaging. + Experience with Good Manufacturing Practices ( GMP ) and Computer System Validation (CSV) regulations, will be vital in… more
- Novo Nordisk (Bloomington, IN)
- …commissioning/validation team, including operational protocol development, to implement compliance with FDA GMP requirements + Draft SOPs for building and ... 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
- Lilly (Indianapolis, IN)
- …Preferences:** + Solid Understanding of Basic Requirements of Regulatory Agencies Such as the FDA , EMEA, DEKRA, And Osha in a GMP environment. + Previous ... horizon. + **Lead by example** and **coach** others in safety, quality , engineering, and continuous improvement. + **Interact** directly with regulatory agencies… more
- Bristol Myers Squibb (Indianapolis, IN)
- …capital projects (value: $10M- $150M), ensuring adherence to budget, schedule, quality , and regulatory standards. * Oversee the design, construction, and ... Qualifications * Expertise in pharmaceutical engineering, including cGMP and FDA /USP/OSHA regulatory requirements. * Proven experience developing and leading… more