Job Posting for Quality Systems Specialist - Document Control at Cardiovascular Systems, Inc.
Summary:
It is the primary responsibility of this position to ensure control of all forms of documentation, facilitating changes in a timely manner with a high degree of accuracy. This individual will have an established working knowledge of document control processes in a FDA QSR and ISO 13485 regulated medical device environment.
Qualifications:
2+ years experience in Medical Device industry
Experience with document control processes (or demonstrated competence)
Must be able to work independently with minimal oversight and guidance
Strong interpersonal skills required, including effective verbal/written communications and professionalism
Ability to effectively manage multiple initiatives simultaneously in a dynamic, fast-paced environment
Detail-oriented with a quality-first work ethic
Proficient in Microsoft Office
Responsibilities:
Leads and maintains the document control element of the Quality Management System (QMS), including associated procedures
Supports and trains other users as needed
Assists with the training element of the QMS
Exemplifies a high standard of quality to the organization
Plays a key role in internal and external audits for the outlined areas of responsibility
Salary.com Estimation for Quality Systems Specialist - Document Control in St. Paul, MN
$93,001 to $114,964
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