JenaValve Technology, Inc. Jobs in United States

The Clinical Safety Specialist contributes to the overall conduct and timely execution of clinical trials by overseeing subject safety and adverse event data reporting. · ...

Provide support to various areas of the quality management system with emphasis on post-market surveillance (Complaint handling). · Bachelor of Science degree in engineering or relevant scientific subject. · 4 + years medical device Quality/Regulatory experience in a medical devi ...

Supervision and development of an assembly team and area conducting Delivery System (Delivery Catheter, Loading Tools, and Introducer Sheath) and THV primary and secondary packaging and labeling. · Effective planning, organization, control, and supervision of manufacturing invent ...

This is a temp-to-hire clerk position in a warehouse environment. The primary responsibility is manual and clerical shipping and receiving duties. · ...

Responsible for performing incoming inspections on incoming materials ensuring compliance with specifications and quality standards. · ...

The Senior Clinical Research Associate will report to the Associate Director, Clinical Programs, and will play a key role in proactively supporting the conduct of pre-market clinical studies and ensure compliance with all regulatory requirements. · 2+ year of experience in clinic ...

The job is a clerk position in a warehouse environment. The primary responsibilities include manual and clerical shipping and receiving duties, material support to production, and inventory transactions. · Perform general warehouse processes including manual and clerical shipping ...

Responsible for timely preparation and submission of organized, scientifically valid global regulatory affairs submissions (clinical, pre-, and post-market applications), query responses and correspondence tracking. · ...

The Senior Clinical Research Associate will report to the Associate Director, Clinical Programs, · a nd will play a key role in proactively supporting the conduct of pre-market clinical studies and ensure compliance with all regulatory requirements.Support site management and int ...

This role involves performing incoming inspections on materials to ensure compliance with quality standards. · Generating non-conforming reports. · Utilizing various measuring devices to assess product quality. · ...

Develop components or subsystems for transcatheter heart valves and delivery systems. · Design and document components and subsystems. · ...

Responsible for timely preparation and submission of organized, scientifically valid global regulatory affairs submissions. · ...

+Applies skill and dexterity in the sewing of tissue and non-tissue components and the tissue processing used to produce medical devices. · Use tools - needles, scissors, forceps, specialized tooling, microscope - to perform assigned steps. · ...

Reporting to the Director of Clinical Affairs, the Manager, Clinical Affairs (CRB) will be responsible for case planning for global clinical trials and collaborating with internal and external stakeholders on CRB process development, execution, and improvement. · This position pr ...

The QAD System Administrator is responsible for the day-to-day administration, · maintenance,and optimization of the company's QAD ERP system.Manage · & maintain QAD ERP environments. · Create · & maintain user accounts, · & roles,& security permissions. · ...

Responsible for performing incoming inspections on incoming materials ensuring compliance with specifications and quality standards. · ...

Working conditions are primarily in a warehouse environment with regular use of phone, computer, and material moving equipment as required. · Perform general warehouse processes including manual and clerical shipping and receiving duties, · ...

Job Title Senior Clinical Research · The Senior Clinical Research Associate will report to the Associate Director, Clinical Programs, · Support site management · Interact with site coordinators · ...

The Manager Clinical Affairs will be responsible for case planning for global clinical trials and collaborating with internal and external stakeholders on CRB process development, execution, and improvement. · ...

Responsible for timely preparation and submission of organized scientifically valid global regulatory affairs submissions. Interacts with internal departments and external representatives. · ...