Demo

Quality Assurance Administrator - Documentation Control

DEKA Research & Development
Manchester, NH Full Time
POSTED ON 5/7/2026
AVAILABLE BEFORE 7/21/2026
Join our dynamic team at DEKA and be part of creating innovative medical solutions! As our QA Admin focusing on Document Control, you'll play a vital role in supporting the QMS through document control processes in our medical device R&D environment. You'll work collaboratively with cross-functional teams to ensure documentation accuracy and accessibility.

Key responsibilities as a QA Admin (Documentation Control):
  • Perform QA document control functions for processing Engineering Change Orders (ECOs) including issuance, distribution, release, training, and archiving, utilizing DEKAs eQMS
  • Support all administrative functions to the QA and Compliance Manager
  • Process training activities, perform review of training records, and coordinate training database
  • Modify and format technical documents according to established SOPs and regulatory requirements
  • Facilitate timely document reviews and approvals with project teams and customers
  • Expedite critical documentation changes to support project schedules while maintaining compliance
  • Support documentation requests during internal and external regulatory audits
  • Support collection, analysis, and trending of QMS data.
  • Support continuous improvement initiatives within document control workflows and the broader QMS
Skills you will need to be successful in this role:
  • Strong attention to detail: your thoroughness ensures documentation accuracy and compliance
  • Excellent organizational skills: you can manage multiple priorities and track numerous documents simultaneously
  • Technical proficiency: you have advanced skills in document formatting and Microsoft Office applications
  • Effective communication: you can clearly articulate documentation requirements to various stakeholders
  • Problem-solving mindset: you identify process inefficiencies and implement improvements
  • Adaptability: you thrive in a fast-paced environment with changing priorities
  • Independence: you can work with minimal supervision while maintaining high-quality standards
  • Collaborative approach: you partner effectively with teams across the organization
Qualifications:
  • Bachelor’s degree
  • 2 years of experience administering processes within a database.
  • Strong written and verbal communication skills.
  • Advanced proficiency in Microsoft Word, including manipulation of headers/footers, page layout control, document sections, orientation, styles, and tracked changes.
  • Strong computer skills with databases and software applications.
  • Project coordination and/or project management experience.
  • Demonstrated aptitude for learning technical information quickly and accurately.
  • Local candidates strongly preferred.
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.

Salary.com Estimation for Quality Assurance Administrator - Documentation Control in Manchester, NH
$84,328 to $104,908
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