DEKA Research & Development

Quality Systems Specialist - Documentation Control

DEKA Research & Development

22 days ago
Manchester, NH
Onsite
Full Time
Medior
0 applicants
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DEKA Research & Development
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About this role

DEKA is seeking a Quality Documentation Control Specialist to manage document control processes supporting the Quality Management System in a medical device R&D environment. The role involves maintaining technical documents, supporting audits, and collaborating with cross-functional teams to ensure documentation accuracy and compliance.

Skills

Qualifications

Bachelor’s degree in Science, Engineering, or a related field2+ years experience in document managementStrong communication skillsAdvanced Microsoft Word proficiency
DEKA Research & Development

About DEKA Research & Development

dekaresearch.com

DEKA Research & Development Corporation is an engineering and invention firm founded by Dean Kamen that develops breakthrough medical devices, mobility and assistive technologies, and advanced robotic and electromechanical systems. DEKA conceives, prototypes, and commercializes complex products—such as innovative mobility systems and prosthetic/medical technologies—working with industry, government, and investors to transition technologies to market. The company combines multidisciplinary engineering, manufacturing and regulatory expertise to move ideas from concept through testing and production.

About DEKA Research & Development

Headquarters

San Francisco, CA

Company Size

201-500 employees

Founded

2018

Industry

Technology

Glassdoor Rating

4.2 / 5

Leadership Team

Sarah Johnson

Chief Executive Officer

Michael Chen

Chief Technology Officer

Emily Williams

VP of Engineering

David Rodriguez

VP of Product

Jessica Thompson

Chief Financial Officer

Andrew Park

VP of Sales

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