- System One (Indianapolis, IN)
- Job Name: Medical Affairs Project Manager Location: Indianapolis, IN Contractor Work Model: Onsite Work Schedule: Mon- Fri 8a- 5pm Full Job Description: ... or 3-5 years of pharmaceutical experience (2 of which is in medical affairs ) + Experience in rheumatology therapeutic area is highly recommended. + Knowledge… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, quality ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units as needed. Works… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …new and marketed biologic and small molecule drug products to assigned project teams, to ensure Otsuka's products are developed/maintained in compliance with global ... CMC and GMP related submissions and inquiries. + Represents CMC RA in project team meetings and provides regulatory guidance and perspective to the cross-functional… more
- Veterans Affairs, Veterans Health Administration (Indianapolis, IN)
- …healthcare engineering advisor, engineer consultant, engineer designer, contract administrator, project manager , construction coordinator, and instructor during ... serves as a Project Engineer at an assigned Department of Veterans Affairs (VA) Healthcare System. This position performs project planning, produces designs,… more
- Fujifilm (Indianapolis, IN)
- …discipline. MS desired. + At least five (5) years' experience as a product manager for Medical IT and/or Imaging product. + Preferred software administration ... Proven track record working with Marketing, Business Development, Engineering/QA, and Regulatory Affairs . + Competitive knowledge of Medical IT and Imaging… more
- Sumitomo Pharma (Indianapolis, IN)
- …a dynamic, highly motivated, and experienced individual for the position of **Senior Manager , Clinical Supply Chain** . The Senior Manager , Clinical Supply Chain ... on multiple clinical programs. In addition, working closely with CMC, Regulatory Affairs , Quality Assurance, Clinical Operations, and /or SMPA external partners and… more
- Grifols Shared Services North America, Inc (Hammond, IN)
- …compliant medical device quality system for R&D and informing project teams of needed updates/changes **Additional responsibilities:** + Represent R&D Compliance ... of, and leads/executes regulatory strategy and tactical decisions from project inception to regulatory approval, including lifecycle management of existing… more
- Tecomet (Warsaw, IN)
- **JOB SUMMARY:** The Quality Systems Manager will provide overall company leadership and direction for Quality Assurance and Regulatory Affairs Systems, ... and facilitate the development of quality systems for a highly regulated medical device industry to achieve customer satisfaction, increase productivity and maximize… more
- Novo Nordisk (Bloomington, IN)
- …Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition ... employees and cross-functional group managers/departments on facility-related issues. Relationships Manager . Essential Functions + Process Leadership and Strategy: +… more
- GE Aerospace (Indianapolis, IN)
- …an industry tailored risk profile and audit methodology. * Assisting the Audit Manager in leading audit project teams, executing control testing, analyzing ... role will be to coordinate with the Internal Audit Manager and other team members to execute the audit...risk based on industry risk profile, and develop a project scope for complex and cross-functional process areas, leveraging… more