Technical Author - Indiana

KBS is seeking a Director, Information Security to serve as the senior operational leader responsible for enterprise-wide security strategy, corporate system protection, and regulated product compliance. · ...

We are seeking a Medical Technical Writer to support our Quality Management System by developing GxP documentation within Veeva QualityDocs. · Migrate legacy content into approved templates ensuring compliance with regulatory requirements. · ...

Role: Validation Engineer – Equipment & CSV (GMP Environment) · Location: Indianapolis, IN · Onsite · Job Description: · Author equipment qualification and validation packages · Plan coordination with equipment manufacturer or supplier for preventative maintenance · Technical r ...

Job Responsibilities: Monitor and analyze manufacturing and equipment performance data to drive continuous improvement and support investigations. · ...

V2X is seeking a Program Chief Engineer for Ground Launched Systems within the Weapons System Integration (WSI) Team in Indianapolis. The Program Chief Engineer serves as the primary technical authority for assigned defense programs. · ResponsibilitiesServe as the technical autho ...

Responsibilities · Serve as process technical lead for aseptic filling, sterile filtration, and packaging operations. · Provide floor-based support for commercial fill/finish manufacturing activities in ISO 5/7 environments. · Lead complex deviation investigations, root cause ana ...

Lilly is a global healthcare leader headquartered in Indianapolis, Indiana. We are looking for people who are determined to make life better for people around the world. · Provide technical oversight and stewardship for peptide and/or oligonucleotide manufacturing processes. · ...

The TSMS Technical Transfer Engineer supports the successful transfer scale-up and lifecycle management of clinical commercial manufacturing processes in a cGMP environment. · ...

An industry-leading manufacturing firm is seeking an Environmental Professional to lead compliance initiatives at a major Indianapolis facility. · ...

The Regulatory Submissions Document Reviewer I is responsible reviewing regulatory documents for various client departments. Responsibilities include providing review of nonclinical toxicology, pharmacology and pharmacokinetic regulatory submission documents to ensure consistency ...

The QA Compliance Specialist implements robust Quality Systems for RLT Indianapolis site considering Novartis and regulatory requirements of the organization.This role contributes significantly to the execution of these systems authors or contributes to the procedures governing t ...

The QA Compliance Specialist implements robust Quality Systems for RLT Indianapolis site considering Novartis and regulatory requirements of the organization. · This role contributes significantly to the execution of these systems, · authors or contributes to the procedures gover ...

· The Manufacturing Engineering Technical Lead will be the technical authority for the supplier management team by integrating all manufacturing engineering activity across the product lifecycle and through the supply chain. The role will lead, manage and develop manufacturing e ...

The QA Compliance Specialist implements robust Quality Systems for RLT Indianapolis site considering Novartis and regulatory requirements of the organization. · This role contributes significantly to the execution of these systems, authors or contributes to the procedures governi ...

We are looking for QA Compliance Specialist, · Implement and execute quality systems at RLT Indianapolis site considering Novartis and regulatory requirements. · This role contributes significantly to the execution of these systems, authors or contributes to the procedures govern ...

The Configuration Management (CM) Specialist supports engineers in complex system software and hardware development ensuring product life cycle data is controlled documented correctly consistently. · ...

We are seeking an experienced MEP QAQC Engineer – Pharma/Life Sciences to join our team in Indianapolis. · Join Our Team · We are seeking an experienced MEP QAQC Engineer – Pharma/Life Sciences to join our team in Indianapolis. · ...

Information Security Assurance Lead · The Information Security Assurance Lead serves as the senior technical authority for information assurance (IA) efforts. · Provide oversight across Assessment & Authorization (A&A), Risk Management Framework (RMF), FISMA compliance, FISCAM au ...

This position is responsible for providing assistance and mentorship in investigations, change proposals, procedure and manufacturing instruction revisions and validations. The Quality Control Representative will assist with periodic self-inspections of the manufacturing area to ...

We are looking for a Technology Leader who will serve as both the technical authority and customer-facing technology lead for complex network solutions. · This role requires deep technical expertise, strong leadership, and exceptional communication skills to ensure customer confi ...

The controls engineer will be part of Customer Technical support, responding to customer needs for technical support. · ...