Jobs at NAMSA

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.

Provide clerical and technical support for laboratory studies: review raw data and photos, update SOPs/protocols/worksheets, generate IACUC submissions, maintain study spreadsheets, initiate nonconformances, interact with clients/auditors, assist scheduling, and meet on-time metrics.

Perform routine microbiology test article preparation, execute tests per NAMSA SOPs, record and review data, operate laboratory equipment, perform environmental monitoring and cleanroom maintenance, respond to monitoring alarms, support test specification preparation and client interactions, and follow GLP/GMP and applicable standards.

Support Study Directors/Principal Investigators in GLP and non-GLP preclinical studies by coordinating study tasks, collecting and entering data, maintaining records and test article accountability, communicating with sponsors and investigators, assisting with protocol generation and technical reports, and managing study documents and logistics.

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.

The Client Success Program Manager serves as the main contact for clients, managing complex programs, resolving issues, and ensuring effective communication across teams to enhance client experiences.

Performs necropsies, routine gross examinations, tissue trimming, specimen shipping, photography and x-ray imaging, and maintains GLP-compliant records, SOPs, and laboratory equipment. Assists with protocol review, calibration/validation of specialized equipment, and other pathology-support duties.

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.

Lead and perform clinical site monitoring and oversight for medical device studies, ensuring human subject protection, GCP and regulatory compliance. Manage site qualification, initiation, interim and close-out visits, documentation (TMF/CRF), metrics tracking, training, safety support, regulatory submissions, audits, and cross-team communication.

Manage and monitor clinical trial sites to ensure human subject protection, GCP and regulatory compliance. Conduct site visits (qualification, initiation, interim, close-out), track enrollment and study metrics, maintain study documents and TMFs, support start-up and safety activities, communicate with investigators and project teams, and provide training and reporting.

Senior Clinical Research Associate contractor responsible for overseeing clinical research activities, monitoring study conduct and compliance with protocols and regulations, managing documentation, and liaising with sponsors and cross-functional teams to support MedTech product development.

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.

Perform routine in vitro test article preparation and testing per SOPs, maintain cell lines/reagents and lab records, conduct environmental monitoring and operate equipment, draft technical documents, ensure GMP/GLP compliance, respond to alarms, and support quality and workflow improvements.

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 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.