21 Cfr 11 Jobs

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 team is hiring a Quality Engineer II to lead design control, risk management, and quality assurance activities for medical and consumer health devices.

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

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.

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.

QRC Group seeks a CSV Specialist experienced in bioprocess validation and vision/inspection systems to lead commissioning, qualification and computerized system validation activities in a pharmaceutical manufacturing setting.

Experienced IT professional needed to deliver onsite L2/L3 support for lab instrument PCs and applications in a regulated pharmaceutical/biotech setting.

Lead the design and operationalization of scalable lab and enterprise data architectures to enable scientific insights and regulatory-compliant data management across AskBio's global lab network.

AbbVie is hiring an IT Technical Specialist to lead and support Quality Labs application projects and integrations that improve lab productivity and regulatory compliance.

Lead oversight and strategic management of clinical records and SOP development at a cutting-edge biotech innovator.

A CSV Engineer II is needed at FUJIFILM Biotechnologies Texas to lead validation efforts for computer systems in a cutting-edge biomanufacturing environment.

Lead eCOA user acceptance testing and operational management for clinical trials at Bristol Myers Squibb in a hybrid full-time role.

Support and maintain laboratory instrumentation and systems at Eurofins Scientific, ensuring compliance and operational excellence.

Lead IT validation strategies and compliance for cutting-edge GxP systems at Dyne Therapeutics, impacting global regulatory adherence in biotech.