Cfr Jobs

The Oregon Department of Emergency Management is hiring Grant Accountants to manage grant fiscal processes, ensure compliance with federal grant rules, and support reporting and reconciliation for OEM grant programs in a hybrid work arrangement.

Lead multi-shift powder filling operations at Abbott Nutrition's Casa Grande plant, driving quality, OEE, compliance and team performance.

Celerion seeks an experienced Clinical Data Manager in Tempe, AZ to manage clinical database setup, cleaning, query resolution, and sponsor-facing data management activities across early- to late-phase studies.

Care Access Research is hiring a Source Document Specialist to design, maintain, and version-control compliant eSource and paper source documents for remote clinical trial operations.

SciTec is hiring an Industrial Security Specialist to manage program security requirements, enforce classified material controls, and support facility compliance at the Boulder, CO office.

Experienced platform-focused IT engineer needed to deploy, operate, and support IT infrastructure at FUJIFILM's new Holly Springs biomanufacturing site while aligning with global IT architecture and regulated compliance.

Agilent is hiring a Clinical Research Associate to monitor investigator sites, ensure GCP-compliant trial conduct, and maintain TMF/eTMF while supporting study start-up through closeout.

DOHMH is hiring an Associate Staff Analyst to manage Mental Hygiene state aid claims, perform reconciliations and financial reporting, and act as the agency's liaison with state offices.

QRC Group seeks an experienced Quality Systems Specialist to manage and improve quality systems, support investigations, and ensure compliance with GMP, FDA 21 CFR Part 11 and data integrity requirements.

The University of Kansas Cancer Center is hiring a Clinical Research Coordinator to coordinate and monitor oncology clinical trials, manage data and regulatory documentation, and support patient-facing research activities.

ActiGraph is hiring a Senior Compliance Specialist to lead QMS and regulatory compliance activities across product development, post-market surveillance, and audits for their medical-grade wearable solutions.

AHRC New York City is hiring a Director, Budget & Planning to lead annual budgeting, forecasting and personnel cost management for its Manhattan finance team.

Experienced document control professional needed to own DMS maintenance, ensure regulatory-compliant records, and support audits for a remote, regulated-healthcare-focused company.

Statistics & Data Corporation is hiring a Principal Clinical Programmer to lead EDC database development, validation, and integrations while serving as a technical SME and mentor for clinical programming teams.

DeepHealth seeks a hands-on QA/RA Project Manager to drive quality, regulatory readiness, and cross-functional delivery for medical device software and digital health products in a fully remote role.

AbbVie is hiring a QA Validation Engineer to lead validation planning, execute validation tasks, and support quality and regulatory compliance at its North Chicago manufacturing facility.

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Lead and mentor the Quality Control team at Hims & Hers' New Albany compounding facility to ensure in-process and final product quality, compliance with USP and cGMP standards, and audit readiness.

Sanford Health is hiring a Research Compliance Specialist in Sioux Falls to manage IRB submissions, maintain clinical trial documentation, and ensure regulatory compliance for clinical research studies.

CORE seeks a hands-on Director of Finance to drive strategic FP&A, audit & internal controls, and grant compliance for a complex international nonprofit portfolio.

Serve as the on-shift security incident commander at Lawrence Livermore National Laboratory overseeing armed protective force operations, tactical response, and regulatory compliance across multi-site facilities.

Lead regulatory strategy and submissions for device and combination products at AbbVie to ensure timely global approvals and compliance.

ResMed seeks a Senior Manager of Design Quality (Digital Product) to lead a product quality team and act as the primary QA representative for software and SaMD projects, ensuring design control, risk management and regulatory compliance.

Acadia Healthcare’s West Lebanon MAT clinic is hiring a licensed Substance Use Counselor to deliver individual and group counseling and support recovery for patients with opioid use disorder.

Experienced clinical supply professional needed to manage forecasting, IRT operations, vendor coordination, and depot/site inventories for Cogent Biosciences' clinical programs.

AbbVie's Waco site is hiring a Senior Automation Engineer to lead design, validation, and lifecycle management of manufacturing control systems to enhance productivity, quality, and safety.

Experienced STARLIMS developer needed to lead configuration, integration, and compliance-focused development of STARLIMS v12+ for a healthcare-focused, regulatory-driven environment.

Experienced healthcare IT product analyst needed to drive requirements, design, and delivery of financial and clinical research solutions for SCRI, supporting oncology clinical trials and enterprise users.

BlueRock Therapeutics is hiring a Director of Clinical Operations Quality to lead SOP and TMF standards, drive clinical compliance and inspection readiness across its advancing cell therapy clinical programs.

The City of Charlotte seeks a Security Operations Supervisor to lead insider-threat training, regulatory compliance, and daily security operations at Charlotte Douglas International Airport.

VahatiCor is hiring a hands-on Quality Engineer with direct catheter device experience and ISO 13485 expertise to lead quality activities for catheter manufacturing and validation.

FUJIFILM Biotechnologies is hiring an Associate Director to lead Cleaning Validation and CQV strategy at its Holly Springs biologics facility, ensuring compliant, risk-based validation for multi-product manufacturing.

Lead validation and qualification efforts at Gerresheimer’s Peachtree City facility to ensure compliant, well-documented manufacturing and support processes for pharmaceutical and medical device products.

Lead the implementation and validation of Emerson DeltaV control systems for regulated biopharma and medical device manufacturing at an employee-owned engineering company based in Kalamazoo, MI.

Abbott's Lingo division is hiring a Quality Engineer II to lead design control, CAPA, and risk-management activities for medical devices and SaMD from our Alameda, CA site.

Experienced publishing specialist needed to manage eSubmission workflows, ensure regulatory-compliant clinical document publishing, and support process and vendor management at AbbVie's North Chicago site.

Lead fiscal operations for Mesa County Public Health by managing accounting, grants compliance, purchasing, contracts, and budgeting for an approximately $12M annual budget.

Lead CPC's technology modernization as Managing Director of Technology, driving secure, compliant, and data-enabled transformation across the organization.

Remote Finance and Medical Records Specialist needed to manage Release of Information workflows, ensure compliant PHI disclosures, and assist finance operations for a US-based healthcare organization.

Lead systems-level solutions and sustaining engineering at Insulet as a Principal Systems Engineer, providing technical leadership across design, post-market support, and regulatory-compliant lifecycle activities.

Abbott seeks a Senior Design Control Software Quality Engineer to validate and maintain Lingo product software and computerized quality systems in compliance with medical device regulations.

Experienced systems engineering leader needed to drive sustaining engineering, root-cause resolution, and regulatory-compliant product improvements for Insulet's wearable drug-delivery platform in a hybrid Massachusetts role.

Abbott is hiring a Software Quality Engineer II in Sylmar, CA to lead software validation, quality engineering, and regulatory compliance for non-product medical device software.

Lead opto-mechanical engineering for ophthalmic diagnostic and visualization devices at Alcon's Lake Forest R&D site, driving high-precision designs, validation, and transition to manufacturing.

Lead and develop a Quality Engineering team in Abbott’s Electrophysiology division to drive manufacturing quality, regulatory compliance, and continuous improvement for Class II/III medical devices.

Trove Brands is hiring a Senior Quality Specialist to lead QMS development and ensure regulatory, analytical, and product quality from R&D through commercialization for sports nutrition and consumer products.

Abbott Neuromodulation seeks a Senior Operations QA Engineer in Plano, TX to drive quality improvement, data analytics, and regulatory compliance across manufacturing operations.

Lead FTZ compliance and operational controls for a busy Dania Beach distribution operation, managing CBP filings, inventory reconciliation, and cross-functional coordination.

Intuitive seeks a senior Supplier Manufacturing Engineer (Plastics or Machining) to lead supplier qualification, DFM, and process controls for mission-critical components used in robotic-assisted surgery.

Crinetics Pharmaceuticals is hiring a Senior Manager to lead clinical data management, SAS programming and external data validation and reporting to support clinical development and regulatory readiness.

AIChE is hiring a Grant & Financial Technology Manager to own grant budgeting, invoicing, compliance, and financial system enhancements that improve reporting accuracy and reduce manual effort.