Document Control Coordinator

ARCH


Job Location:

Elmhurst, NY - USA

Monthly Salary: $ 26 - 30
Posted on: Yesterday
Vacancies: 1 Vacancy

Department:

Manufacturing

Job Summary

Primary Responsibilities

  • Maintains updates and manages QCBD (Quality Collaboration By Design) document file system.
  • Organizes and oversees QCBD training related to the Quality Management system.
  • Executes document approval release archival and obsolescence per the quality system.
  • Modifies and documents changes to Quality System Procedures.
  • Functions as an information source for production and other departments when critical quality documentation issues arise.
  • Submits and processes change orders under ISO 13485 and FDA 21 CFR Part 820.
  • Monitors device history records process to meet ISO 13485 and FDA 21 CFR Part 820.
  • Performs device history record review.
  • May perform data entry and trend analysis and initiate negative trend corrective actions.
  • Works with management in all company areas to effectively resolve document errors/omissions.
  • Updates and maintains product DMRs.
  • Maintains staff training records and working with supervision ensuring that all QCBD training is to current requirements.
  • Accurately enters data into EPICOR.
  • Provides document support for internal and external audits as needed.
  • May educate and instruct plant personnel in recommended quality control testing and equipment methods and acceptable documentation practices.
  • Assists other departments with ad-hoc projects and serves as a back up per business needs.
  • Other duties as assigned.

Qualifications

  • Associate degree in applicable technical discipline is strongly preferred or equivalent
  • or two (2) to three (3) years of experience in medical device manufacturing industry and/or document management systems and/or training
  • or equivalent combination of education and experience.
  • Basic regulatory knowledge in medical regulations.
  • Accuracy of typing skills and extreme attention to detail are required.
  • Knowledge of ISO 13485 Quality Management System & FDA 21CFR 820 Regulations.

Shifts Available: 1st shift

Salary Range: $26.00 - $30.00/hr based on experience

Equal Employer Opportunity

ARCH is an Equal Opportunity Employer who wholeheartedly supports diversity in the workplace as basic premise for business success. We do not discriminate on a basis of race religion color sex gender identity sexual orientation age non-disqualifying physical or mental disability national origin veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications merit and business need. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.


Required Experience:

IC

Primary ResponsibilitiesMaintains updates and manages QCBD (Quality Collaboration By Design) document file system.Organizes and oversees QCBD training related to the Quality Management system.Executes document approval release archival and obsolescence per the quality system.Modifies and documents c...

About Company

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ARCH is a contract manufacturer with advanced precision-machining capabilities serving the medical, aerospace and defense, energy, and other industrial markets.

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