Jobs at NAMSA

Manages procurement, qualification, validation, maintenance, troubleshooting, and documentation for laboratory measurement and test equipment. Develops protocols, reports, SOPs, risk assessments, and change controls; investigates failures and nonconformances; supports electronic data compliance, building expansion validations, engineering systems, audits, training, and equipment monitoring. Partners with laboratories and IT to maintain compliant, reliable testing operations.

Prepares and processes biological tissues for pathology review, including fixation, embedding, microtomy, frozen sectioning, mounting, and histochemical staining. Performs quality control, tissue trimming, grossing, necropsy support, specimen shipping, equipment calibration, recordkeeping, and laboratory maintenance under GLP and departmental SOPs. The role also handles biohazard disposal, slide and cassette labeling, sample archiving, and troubleshooting of staining and tissue-processing procedures.

Performs routine microbiology laboratory testing, product preparation, calculations, data recording, equipment checks, environmental monitoring, and cleanroom disinfection according to SOPs. May operate laboratory equipment, respond to monitoring alarms, and conduct specialized testing. Requires compliance with GLP/GMP practices and applicable USP, ISO, CTFA, and FSA guidelines.

Coordinates and leads preclinical medical device studies from initiation through completion. Serves as Study Director for GLP and non-GLP studies, ensuring regulatory and quality-system compliance. Manages study designs, schedules, budgets, multidisciplinary teams, client communication, data analysis, reporting, record archiving, and IACUC submissions. Interacts with clients, regulators, auditors, and subcontractors while supporting scientifically sound study execution and documentation.

Coordinates and leads preclinical medical device studies from initiation through completion. Responsibilities include study design, client communication, regulatory and IACUC submissions, GLP compliance, data analysis, scientific reporting, record archiving, and multidisciplinary team management. The role may serve as Study Director or Principal Investigator and involves interaction with clients, auditors, inspectors, regulatory bodies, and laboratory animals.

Manages clinical operations, staff workload, project delivery, regulatory compliance, client expectations, budgets, recruiting, and team development for medical device clinical programs. Coordinates clinical, biostatistics, and data management activities; supports proposals, business development, conferences, process improvement, and regulatory inspections. Requires knowledge of clinical trial processes, medical device development, global regulations, and Good Clinical Practices.

Receives and processes test samples and laboratory requests in LIMS, archives reports and test materials, and prepares outgoing reports by copying, faxing, or emailing. Provides receptionist coverage as needed and performs accurate clerical, data-entry, and customer-service tasks in a GLP/GMP laboratory environment.

Manages clinical research studies involving site monitoring, human subject protection, GCP and regulatory compliance. Coordinates site qualification, initiation, interim and close-out visits; oversees study documentation, metrics, training, audits, budgets, safety activities and regulatory submissions. Supports protocol development, data management, core laboratory operations, literature reviews and trial registration. Mentors CRAs and communicates study performance, risks and progress to investigators, clients and internal teams.

Manages clinical studies from site selection and regulatory submissions through enrollment, monitoring, data quality review, and close-out. Develops study materials, tracking tools, project plans, and clinical study reports; coordinates cross-functional teams, investigators, sponsors, core laboratories, and safety committees. Ensures GCP, protocol, SOP, regulatory, audit, and Trial Master File compliance. Supports clinical audits, inspections, site issue resolution, and study-system implementation. Travel is typically 20–30%.

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.

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.

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.

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.