- Abbott (Houston, TX)
- …Spinal cord stimulator on the market, Proclaim (TM) DRG Neurostimulator, the only FDA approved DRG therapy and a market leader in radiofrequency ablation therapy, ... product developments *Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, company policies, operating procedures,… more
- Actalent (Menomonee Falls, WI)
- …requires the creation of safety programs that align with OSHA, FDA , and pharmaceutical industry standards. Responsibilities + Develop and implement site-specific ... Skills + Proficiency in safety protocols and standards, including OSHA and FDA regulations. + Ability to conduct thorough risk assessments and implement safety… more
- Cardinal Health (Columbus, OH)
- …manner while enforcing Cardinal Health compliance and regulations concerning OSHA, DEA, FDA , State and local authorities. + Enforces Cardinal Health compliance and ... regulations for OSHA, DEA, FDA , state and local authorities, primary facility contact for QRA compliance. + Assist with EHS audits, conduct Job Safety Observations… more
- Nanobiosym, Inc. (Cambridge, MA)
- …the creation of a validation protocol (IQ, OQ, PQ) that comply with FDA regulations. + Provide troubleshooting focus and direction for the team with details ... process control + Electromechanical experience is required + Recent experience with an FDA regulated (21 CFR 820) and/or ISO 13485 environment + Good communication… more
- BGB Group (New York, NY)
- …channel best practices, as well as expected audience behaviors, and maintains FDA compliance + Community Management: Monitors and manages user engagements on ... platforms + Can write a creative brief + Familiar with client MRL and/or FDA requirements, and has experience blending social media best practice to lead brief… more
- Nanobiosym, Inc. (Cambridge, MA)
- …steps. + Develop and implement validation protocols (IQ/OQ/PQ) that comply with FDA regulations. + Provide troubleshooting focus and direction for the team with ... statistical process control + Recent experience with medical device development, in an FDA regulated (21 CFR 820) and/or ISO 13485 environment + Strong written and… more
- Allucent (Cary, NC)
- …areas. Application Deadline: 23 January 2026 What You'll Do: + Gain exposure to FDA and ICH guidance as internal or client projects demand + Assist with drafting ... modeling reports, INDs, clinical pharmacology sections of NDAs, Investigator Brochures, FDA briefing packages, and other clinical and regulatory documents +… more
- State of Georgia (Bulloch County, GA)
- …of assigned staff and/or program. . Learns to report compliance findings to the FDA , USDA, and others; results determine the ability to move products. . Learned to ... experience to assist and guide colleagues and management. + Performs State/ FDA Contract Inspections, HACCP Inspections, Shellfish Inspections, and other specialized… more
- Nanobiosym, Inc. (Cambridge, MA)
- …Lead molecular diagnostic assay development in a hands-on manner through successful FDA submission + Manage and contribute to regulatory documents + Project ... managerial and leadership expertise in assay development + Strong understanding of FDA and global regulatory requirements + Prefer commercial assay experience +… more
- Vantage Specialty Chemicals (Deerfield, IL)
- …Governance:** + Ensure ERP and related systems meet global compliance requirements (eg, FDA , GxP, REACH, ISO). + Lead master data governance, access control, and ... across time zones and functions. + Practical understanding of compliance ( FDA , GxP, ISO), MRP, batch processing, and manufacturing workflows. **Working Conditions**… more