- Fujifilm (Indianapolis, IN)
- …States. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... the Endoscopy space. The role of the Business Development Manager is to understand and define our internal and...marketing organization. The incumbent is responsible for supporting the product management group including, but not limited to market… more
- Biomat USA, Inc. (Merrillville, IN)
- …Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed. Duties include: Under the direct supervision of the ... Associate** **Summary:** Under the direct supervision of the Quality Systems Manager , perform quality assurance and Training functions to ensure compliance with… more
- Fujifilm (Indianapolis, IN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... variable factors which may include customer impact, HCUS business priorities and regulatory requirements. Provides to assistance to all connected teams on technical… more
- Novo Nordisk (Bloomington, IN)
- …from process and formulation to clinical and commercial biomanufacturing and drug product fill/finish and packaging. The Bloomington campus is a recognized facility ... and automation, packaging, capital projects, while maintaining compliance with regulatory standards. Process Engineering focuses on developing processes to minimize… more
- Fujifilm (Indianapolis, IN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... to: customer facing course material, instructional "how to" videos, product simulations, etc. + Responsible for executing all aspects...in the event of Senior II, Lead SSAT and manager absence. + Maintain close contact with customers for… more
- Novo Nordisk (Bloomington, IN)
- …from process and formulation to clinical and commercial biomanufacturing and drug product fill/finish and packaging. The Bloomington campus is a recognized facility ... and automation, packaging, capital projects, while maintaining compliance with regulatory standards. Process Engineering focuses on developing processes to minimize… more
- Reckitt (Evansville, IN)
- …R&D or scientific environment. + Strong understanding of R&D processes in product development, formulation, clinical, or regulatory contexts. + Experience with ... work spans so many different businesses, from Research and Product Development to Sales, you'll keep learning exciting new...meet compliance, data integrity, and security standards (eg, GxP, FDA 21 CFR Part 11). 3. Project Delivery +… more
- Fujifilm (Indianapolis, IN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... sell additional products and options. + Work Hospital Relations Manager , National and Government Accounts to develop relationships and...for new equipment and option sales. + Work with Product Managers to conduct product demonstrations and… more
- Novo Nordisk (Bloomington, IN)
- …integrity and ensure compliance with company SOP's, specifications, as well as cGMP, ICH, FDA , EMA regulations or guidelines + Leads regulatory and client audits ... from process and formulation to clinical and commercial biomanufacturing and drug product fill/finish and packaging. The Bloomington campus is a recognized facility… more
- Novo Nordisk (Bloomington, IN)
- …integrity and ensure compliance with company SOP's, specifications, as well as cGMP, ICH, FDA , EMA regulations or guidelines o Leads regulatory and client audits ... from process and formulation to clinical and commercial biomanufacturing and drug product fill/finish and packaging. The Bloomington campus is a recognized facility… more