Regulatory Associate - Indianapolis

The Regulatory Associate leads the global marketing authorization submission management processes and partners with Scientists to create and manage submission content. · ...

The GRA-CMC Regulatory Associate leads the various aspects of global marketing authorization submission management processes. The Regulatory Associate also partners with GRA-CMC Scientists to help create and manage submission content, · The Regulatory Associate will triage and ma ...

We are hiring a Regulatory Associate for one of our clients.The Central Regulatory Registration (CRR) Submission Publisher creates and maintains US regulatory registrations. · ...

+This role is accountable for operational and technical registration management processes supporting expedited delivery of safe effective products to patients. · This includes providing regulatory drug development expertise leading registration management process providing electr ...

The CMC (Chemistry, Manufacturing and Controls) Regulatory Specialist has the responsibility to support new product approvals, · existing product renewals and post-approval changes for global registrations through document distribution · and internal database maintenance.This inc ...

This role is accountable for the operational and technical registration management processes that support the expedited delivery of safe and effective products to patients. · This is accomplished through a strong working knowledge of regulations, guidance's and regulatory precede ...

Ability to publish eCTD global submissions and maintain regulatory data and processes in quality systems. · Being on a temporary contractor assignment at Lilly means working in an innovative culture where you have the opportunity to support the work of thousands of others around ...

This role is accountable for the operational and technical registration management processes that support the expedited delivery of safe and effective products to patients. · ...

This role is accountable for the operational and technical registration management processes that support the expedited delivery of safe and effective products to patients. · Provide Regulatory & Drug Development Expertise Lead the registration management process by providing exp ...

The Regulatory Associate will exemplify excellent technical writing skills and develop productive working relationships with Manufacturing Quality Engineering and client teams.The Associate will demonstrate exceptional attention to detail and the ability to synthesize complex tec ...

We unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understa ...

We are looking for an Associate, GSC Regulatory who will work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences. · ...

We are looking for a Scientific Communications Regulatory Medical Writer to join our team. The ideal candidate will have experience in technical regulatory scientific writing and be able to communicate effectively with cross-functional teams. · Create content strategy for writing ...

We are looking for a Medical Writer to join our team at Lilly. The successful candidate will work with cross-functional teams to develop documents intended for regulatory audiences. · ...

We are looking for individuals who are determined to make life better for people around the world. · Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. · ...

The Quality & Regulatory Compliance Specialist II is responsible for conducting research and interpretation of medical device QMS and accreditation/regulatory standards. The position also involves execution of a Quality Management System and Regulatory Compliance Program. · Regul ...

The Quality and Regulatory Specialist is responsible for providing guidance and support to the TRIMEDX Field Operations team to assure that they maintain a robust, standardized, and effective Quality Management System which complies with applicable regulatory and quality standard ...

We are seeking an experienced Policy Vice President to join our State & Policy Affairs department. · The ideal candidate will contribute to the execution of our strategies in pursuit of objectives related to regulation of the insurance marketplace, analysis of legislative and reg ...

We are seeking an analytical lab technician with strong analytical chemistry expertise to join our team. · Minimum of an Associate Degree in a science related field, BS preferred. · General knowledge of chemistry. · ...

This role is for a contractor to produce compliance data for accreditation and regulatory surveys.The Quality and Regulatory Compliance Analyst will work directly with the Quality team as well as field operations to drive reporting analysis data integrity regarding compliancy to ...