Quality Document Sys Mgmt Coord 2 : 343008

Full Time
Vernon Hills, IL
Posted
Job description
For certain roles at at this client, assignment is contingent upon the Employer of Record’s receipt of sufficient proof that you are fully vaccinated against COVID-19 (meaning two weeks have passed after the last injection of Pfizer/Moderna or two weeks after receipt of the J&J). In some locations, testing for COVID-19 may be available and/or required. Requests for accommodation will be considered pursuant to applicable law.

CorTech is seeking to hire a Quality Document Sys Mgmt Coord 2 for our client in Vernon Hills, IL!
Benefits Available!
Weekly Pay!
$22.00/Hour
Shift: 1st Shift
5 day work week - 4 days onsite (hybrid)
We work remote on Fridays.
Monday, Tuesday, Wednesday, Thursday from 8:00 am to 4:30 pm onsite.

Business Casual Attire/Appropriate attire:
slacks, khakis, dressy capri pants and crop pants, mid-length skirts, dresses (nylons optional)

  • 3 must have:
o Advanced level experience using Microsoft Office (Excel, Word, Access Database)
o Electronic document management experience (SAP, MasterControl, Siemens TeamCenter)
o Learning Management Systems (updating training requirements)

Top skills would be experience in an Admin role for a fast-paced environment, ability to multi-task, advanced level in Microsoft office, attention to detail, and a commitment to

Using Master Control and Learning Management skills as well

Essential Duties and Position Responsibilities:
  • Serve as the Electronic Document Management System (EDMS) and Learning Management System (LMS) administrator (e.g., maintain accurate users, assign passwords and privileges, update training requirements, etc.)
  • Ensure timely, accurate and efficient preparation and management of documents
  • Control the numbering, sorting, filing, storing and retrieval of both electronic and hard copy documents
  • Process changes via the EDMS and DCN systems
  • Provide database navigation and troubleshooting support for the EDMS, LMS and paper based DCN system)
  • Assist managers to ensure required training is assigned and documented
  • Update V. Mueller Product Database (VMPD)
  • Provide documentation and training compliance metrics as requested
  • Maintain central device master documentation
  • Maintain records in accordance with record retention policies.
  • Interface with internal and external auditors during review of the applicable quality management sub-systems (i.e., those pertaining to documentation, change control, and training)
  • Continuous improvement of the change control, documentation control, and training systems.
  • Successful completion of projects assigned by management to support business imperatives.
  • Other duties as assigned

Qualifications, Knowledge, and Skills Required:

  • Associate degree preferred, high school diploma or equivalent required.
  • Excellent verbal and written communication skills.
  • Strong collaboration across business functions.
  • Ability to aggressively drive results in multiple projects simultaneously.
  • Use of Microsoft Office software to generate formal procedures, control logs and databases.
  • Two years of relevant work experience required, preferably in a regulated medical device or pharmaceutical environment.
  • Understanding of blueprints, standard operating procedures, and overall documentation systems.

Summary / Purpose of Position:
This role is responsible for the administration and coordination of the change control, documentation and training
systems for Client Surgery’s IP and V. Mueller platforms. BD04123JD BD04123JD

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