Job Openings >> Document Control Specialist
Document Control Specialist
Summary
Title:Document Control Specialist
ID:1678
Department:Quality
Location:Wolcott, CT
Description
Biomedical Innovations is currently seeking an experienced Document Control Specialist to join our Quality Department in Wolcott, CT. This position is responsible for processing Document and /or Engineering Change Orders (DCO / ECO) and maintaining control over records that are part of the Quality System, providing training to employees on issues related to document and record control, and ensuring document and record control procedures are in compliance with ISO and FDA’s QSRs. The position has the authority to identify deficiencies in ECNs and quality records and where appropriate, recommend corrective and preventative actions.

ESSENTIAL Responsibilities Include:
  • Responsible for keeping current and knowledgeable of the Company’s quality policy and applicable quality objectives; provides support to achieve objectives.
  • Process ECNs in a timely manner, according to the Company’s quality system procedures.
  • Oversee the quality records and logs; ensure they are retained according to the regulatory and quality system requirements.
  • Responsible for improving the efficiency of Document Control while maintaining regulatory compliance for all activities that are part of Document Control.
  • Prepare metrics for document control and provide periodic updates.
  • Follow and enforce compliance to the Company’s quality system and regulatory body requirements per ISO 13485 and FDA 21 CFR 820 as applicable to Document and Record Control.
  • Timely electronic distribution of latest revision level documentation to all appropriate users and ensure removal of obsolete documentation.
  • Coordinate Change Control Board Meetings, maintaining agenda, minutes, and schedule.
  • Regular attendance.
  • Abide by all safety and security rules set forth by the company and regulatory agencies.

Minimum Qualifications:
  • Associates degree in business is preferred.
  • Previous Document Control is strongly preferred
  • Strong knowledge of FDA’s QSRs, ISO 13485:2016 related to document and record control.
  • Experience as a change analyst desired.
  • Excellent organizational skills with high level of detail orientation.
  • Ability to work well under pressure, to handle multiple tasks, and to meet aggressive deadlines.
  • Experience reading and understanding regulations, standards, drawings and procedures.
  • Proficient computer skills with documentation related databases and Microsoft Office (Word and Excel).
Great benefits offered, including medical, dental, 401K, education assistance and more!

Biomedical Innovations is an Equal Opportunity Employer; and considers applicants for all positions without regard to race, color, religion, creed, gender, gender identity, national origin, age, disability, marital or veteran status, sexual orientation, or any other legally protected status. In addition, Biomedical Innovations will provide reasonable accommodations for qualified individuals with disabilities.If you need assistance with completing the online application process, please call Biomedical Innovations at (716) 847-7592.
 
This opening is closed and is no longer accepting applications
Powered by ApplicantStack
CONTACT US
Nissha Medical Technologies
400 Exchange Street
Buffalo, NY 14204
Nissha Medical Technologies is the medical devices business unit and wholly owned subsidiary of Nissha Co. Ltd., a Japanese publicly held company based in Kyoto, Japan (TSE:7915).
Copyright 2020 Nissha Medical Technologies. All rights Reserved
The OEM trademarks identified herein are the trademarks of the respective OEMs, and not Nissha Medical Technologies. Nissha Medical Technologies disclaims any affiliation, connection or association between it's products and those of the respective OEMs.