Quality Assurance Administrator Documentation Control

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profile Job Location:

Manchester, CT - USA

profile Monthly Salary: Not Disclosed
Posted on: 2 days ago
Vacancies: 1 Vacancy

Job Summary

Join our dynamic team at DEKA and be part of creating innovative medical solutions! As our QA Admin focusing on Document Control youll play a vital role in supporting the QMS through document control processes in our medical device R&D environment. Youll 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:
  • Bachelors 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 DEKAs 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.

Required Experience:

Junior IC

Join our dynamic team at DEKA and be part of creating innovative medical solutions! As our QA Admin focusing on Document Control youll play a vital role in supporting the QMS through document control processes in our medical device R&D environment. Youll work collaboratively with...
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About Company

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DEKA Research and Development is perhaps best known for its founder and president Dean Kamen -- and for the Segway Personal Transporter he invented. DEKA is a design and engineering firm that develops innovative technologies, many of them in the field of medical devices. The Segway it ... View more

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