Laboratory Technician & Study Director Assistant W/M

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.

We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry’s premier provider. We provide support for clients during every step of the product development lifecycle and beyond.

Come and work for an organization with the:

Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the

Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core

Values:

• Act with integrity in everything we do.
• Provide best-in-class customer experiences.
• Develop superior talent and deliver expertise.
• Respond with agility and provide timely results.
• Embrace collaboration, diverse perspectives and ideas.

Job Description:

• Primarily involved in various testing activities in accordance with SOPs, and utilizing applicable work instructions, standards or guidelines.
• May be responsible for extractions, test article and control preparation, solution preparation.
• Clean glassware and prepare reagents for use in laboratory testing.
• Perform routine disposal of laboratory waste including disposal of test articles.
• May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping.
• Accurately collect and record raw data in logbooks and on worksheets.
• Review raw materials and final finished media for conformance with applicable material specifications and SOPs.
• Maintain clean workspace, testing supplies, and equipment.
• May be responsible for checking laboratory equipment and respond to continuous monitoring alarms. If needed, the associate will respond in accordance with criteria outlined in Standard Operating Procedures.
• Will be required to operate specified laboratory equipment.

•    Assists Study Directors with all aspects of preclinical animal studies
•    Assists in step up of animal studies, including planning, ordering, and preparing of materials and paperwork
•    Assists with data collection, documentation and analysis, data review (QC), database entry, and generating data
•    Assists with the reporting of study results
•    Assists with archiving of study records and materials
•    Handles logistical responsibilities as they relate to client materials inventory, specimen shipment, and documents, including the maintenance of accurate chain of custody documentation
•    Reviews related documents for consistency and regulatory compliance.
•    Interacts as needed with clients, auditors, inspectors, subcontractors, consultants, and other individuals or departments.
•    Provides clerical/administrative assistance to general facility management
•    Ensures compliance with Good Laboratory Practices (GLP) standards
•    Other duties as assigned.

Qualifications & Technical Competencies: