Data & Quality Review I - Indianapolis, IN

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 Regulatory Submissions Document Reviewer I is responsible reviewing regulatory documents for various client departments. · Provide review of nonclinical toxicology, pharmacology, and pharmacokinetic regulatory submission documents to ensure consistency, clarity, and accuracy ...

Begin a fulfilling career with the State of Indiana by joining one of the largest employers in the state, offering a range of opportunities across 60+ agencies. · This role reviews SNAP benefit approvals to ensure the process was completed correctly and all required documents wer ...

We're hiring a Quality Assurance Specialist to focus on Product Quality and uphold compliance with internal/external standards, regulations, policies, and procedures.This individual will review production and testing records related to the production of bone marrow and bone marro ...

Ossium's Quality Assurance Specialist will review production and testing records to ensure compliance with internal/external standards, regulations, policies, and procedures. · Review technical production and testing records and identify deviations, non-conformances, and complian ...

Lilly is looking for a Quality Management Review Lead to drive the design, implementation, and continuous improvement of management review frameworks and performance health systems across Lilly's Global Quality organization. · ...

The Associate Director – Global Quality Management Review Lead will drive the design, implementation, and continuous improvement of management review frameworks and performance health systems across Lilly's Global Quality organization. · ...

This is a high-impact leadership role at the center of our quality operations. As the Quality Manager, Batch & Donor Record Review, you'll lead the team responsible for donor eligibility and production batch record review within a 21 CFR 1271 and AATB-accredited environment, · en ...

This is a high-impact leadership role at the center of our quality operations. As the Quality Manager, Batch & Donor Record Review, you'll lead the team responsible for donor eligibility and production batch record review within a 21 CFR 1271 and AATB-accredited environment, · Le ...

We are seeking a QA Compliance Specialist with 8+ years of experience in a GMP-regulated biopharmaceutical environment. GMP Experience. · Quality Assurance Experience. · ...

The QA Compliance Specialist implements robust Quality Systems for RLT Indianapolis site considering company and regulatory requirements of the organization. · Supports the development and oversight of robust quality systems, including both implementation and operation at site le ...

Lead and support project teams in the development of Job-Specific Quality Plans. · ...

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 ...

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 Quality Assurance Coordinator (QAC) position is focused on maintaining local compliance with State, Federal and BrightSpring Health requirements. · ...

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 ...

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 Loan Operations Assistant provides exceptional customer service by responding to questions providing information and assistance to ensure that accounts are serviced in an accurate and timely manner. · Responsibilities include booking servicing collateral review and/or imaging ...

+ Job summary · Assist Project Teams: Leads Project Teams in developing the Job Specific Quality Plan. Reviews Construction Documents, Specifications, Shop Drawings, and Submittals with the intent to identify challenges and opportunities. · + ResponsibilitiesL eads project Qualit ...

Strengthen the foundation of Ossium's donor documentation processes by handling communication between recovery partners, medical reviewers and quality assurance staff using our electronic document tracking system. Manage document intake and organize the donor records in preparati ...