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Regulatory Affairs Jobs in Indiana

1 - 9 of 9
1 - 9 of 9
Search Results - Regulatory Affairs Jobs in Indiana
Proclinical Staffing-Indianapolis
Regulatory Affairs, Project Manager - Contract - Remote, Indianapolis Proclinical is looking for a detail-oriented and strategic Regulatory Project Manager to support a project with one of our clients in their Clinical Trial Patient Engagement Team...
mindmatch.ai -
Eurofins USA PSS Insourcing Solutions-Indianapolis
Job Description Leads preparation, technical, and regulatory review and finalization of CMC sections for global CTA submissions Takes a proactive role in the critical review of molecule specific GRA-CMC development strategies and submission...
resume-library.com -
Bloomington (IN)
Overview: The Regulatory Affairs Specialist I at Cook Inc. is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified Class I, II, III and IV medical devices in specific markets. In addition...
icims.com -
Bloomington (IN)
Affairs department is accountable for the direct management and guidance regarding the organization's cGMP compliance and regulatory affairs for biologics, sterile injectables, cell and gene therapy, inhalation manufacturing and analytical services...
tiptopjob.com -
Bloomington (IN)
leading, and collaborating with cross function teams including engineering, production, clinical, and regulatory affairs.  •  Provide leadership in the understanding of medical device regulations and best practices.  •  Must maintain all training requirements...
icims.com -
Bloomington (IN)
Expansion Head. Member of the Senior Leadership Team for the FFEx. Interacts with global counterparts in other FFEx projects as well as with Manufacturing Development, Supply Chain, Regulatory Affairs, Quality Assurance. Essential Functions...
tiptopjob.com -
Bloomington (IN)
building relationships with other functional personnel (Regulatory Affairs, Manufacturing Engineering, Supplier Engineering, Quality Assurance, Operations, R&D).  •  May manage project/task timelines, resources and responsibilities to achieve team...
icims.com -
Ellettsville
audits (e.g. FDA, Notified Body, etc.)  •  Drive continuous improvement efforts through facilitating, leading, and collaborating with cross function teams including quality, engineering, production, clinical, and regulatory affairs.  •  Provide leadership...
icims.com -
Bloomington (IN)
degree in Regulatory Affairs; or experience of such kind and amount as to provide a comparable background.  •  Minimum 5 years’ experience in the field of Regulatory Affairs in the medical device industry preferred.  •  Must be proficient with Microsoft Word...
icims.com -

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