Jobs at NAMSA

Manage procurement, qualification, requalification, validation, maintenance, and documentation of laboratory measurement and test equipment (M&TE). Troubleshoot equipment issues, ensure regulatory and 21 CFR Part 11 compliance, train staff, maintain equipment records, and support software/monitoring systems.

As a Senior HR Business Partner, you will lead HR initiatives, support recruitment, mentor staff, analyze workforce data, and ensure compliance in HR practices while collaborating with senior management.

Manage and improve processes for Individual Case Safety Reports (ICSRs), CECs, and DMCs; intake, analyze, code (MedDRA), and enter adverse event data into EDC and safety databases; write narratives and aggregate reports; support SOPs, QA, and regulatory submissions; coordinate CEC/DMC activities; mentor junior staff; and contribute to system design, metrics tracking, and study-specific safety documentation.

Perform routine microbiology test article preparation, execute tests per SOPs, collect and record raw data, operate lab equipment, perform environmental monitoring and cleanroom disinfection, respond to monitoring alarms, and follow GLP/GMP procedures. Support lab operations and other duties as assigned.

The Microbiology Technologist performs routine testing and product preparation, accurately records data, monitors lab equipment, and maintains cleanroom environments as per SOPs.

The Principal Lab Technician is responsible for test article preparation, executing routine tests, conducting data analysis, maintaining lab supplies, and adhering to regulatory guidelines in a GMP/GLP environment.

Manage and monitor clinical (medical device) study sites to ensure participant protection and GCP/regulatory compliance. Perform on-site and remote monitoring, site start-up and close-out activities, document and metrics management, training, safety support, regulatory submissions, and liaison with investigators and project teams. Role is field-based with high travel and requires French fluency.

Perform routine accounts payable tasks including invoice verification, purchase order and terms reconciliation, supplier communication, GL coding, outgoing payments, supplier statement reconciliation, and use tax recording to ensure timely, accurate payments.

Perform routine microbiology test article preparation and testing per SOPs, accurately record raw data, operate and check laboratory equipment, respond to monitoring alarms, perform environmental monitoring and cleanroom cleaning/disinfection, and support GLP/GMP testing activities.

Support pre-clinical study conduct and administration under Study Director oversight. Responsibilities include data collection and entry, record keeping per SOPs, assisting study planning/protocols, coordinating study tasks, communicating with sponsors and investigators, maintaining inventory and specimen chain-of-custody, and assisting report generation.

Support Study Directors and Principal Investigators in preclinical study coordination: collect and document data, assist study planning and protocol generation, maintain records and inventory, communicate with sponsors and staff, prepare reports and manage specimen/document custody, and perform other lab administrative duties per SOPs.

Manage MedTech projects end-to-end as the client liaison: define scope, plan schedule/budget/resources, ensure quality and QS compliance, run project setup and closure, handle financials and change orders, support audits and CAPAs, and drive project management best practices while mentoring team members.

Support and coordinate preclinical medical device studies from initiation through completion, serve as Study Director for GLP and non‑GLP studies, prepare IACUC protocols, ensure regulatory and quality compliance, analyze and report data, interact with clients and regulatory bodies, and perform study procedures as needed.

Lead and manage medical device projects across the full lifecycle: staffing, planning, budgeting, scheduling, risk management, client liaison, regulatory and quality compliance (QS/GLP/GCP/GMP), project setup and closure, metrics/reporting, and lessons learned. Support audits, change orders, and mentor team members while driving PM best practices and continuous improvement.