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DOCUMENT CONTROL SPECIALIST

In Rhode Island / United States

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DOCUMENT CONTROL SPECIALIST   

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JOB TITLE:
DOCUMENT CONTROL SPECIALIST
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Warwick Rhode Island / United States

JOB DESCRIPTION :
Pay rate - $27.94/hr

Must Haves;
Electronic Systems
Corrective Action
Micrrosoft Planner, List , Sharepoint and heavy Excel.

Summary/Purpose of Position: To maintain compliance with scheduled performance assessments. To resolve supplier quality problems and improve supplier corrective action responses.

Essential Duties and Position Responsibilities:
- Electronic system data entry (ASL updates, supplier audit file upload, etc.).
- Assist suppliers with entering information into electronic supplier change request portal.
- Coordinate the completion of supplier surveys, self-evaluations and supplier profile documentation.
- Issue and manage Supplier Corrective Action Responses (SCAR) including the maintenance of the SCAR Tracking Log.
- Conduct other Quality Control Projects as assigned by the managers of Supplier Quality Engineering and Quality Systems.

Qualifications, Knowledge and Skills Required:
- Preferred working knowledge of medical device manufacturing systems, ISO 13485 and FDA regulations.
- Minimum of 2 to 5 years experience in a supplier quality/supplier auditing capacity or equivalent preferred or equivalent quality function.
- Wide range of experience in different businesses: Medical Devices, Combination Devices, Pharmaceutical/API/Polymers, Calibration, Test Laboratories, Human/Animal Grafts, Injection Molding, and Packaging/Labeling (preferred)
- Strong experience with MS 365 office products.

Position Details

May 17, 2021
S16204861075207281
Rhode Island / United States
Warwick
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

DOCUMENT CONTROL SPECIALIST    Apply

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Pay rate - $27.94/hr

Must Haves;
Electronic Systems
Corrective Action
Micrrosoft Planner, List , Sharepoint and heavy Excel.

Summary/Purpose of Position: To maintain compliance with scheduled performance assessments. To resolve supplier quality problems and improve supplier corrective action responses.

Essential Duties and Position Responsibilities:
- Electronic system data entry (ASL updates, supplier audit file upload, etc.).
- Assist suppliers with entering information into electronic supplier change request portal.
- Coordinate the completion of supplier surveys, self-evaluations and supplier profile documentation.
- Issue and manage Supplier Corrective Action Responses (SCAR) including the maintenance of the SCAR Tracking Log.
- Conduct other Quality Control Projects as assigned by the managers of Supplier Quality Engineering and Quality Systems.

Qualifications, Knowledge and Skills Required:
- Preferred working knowledge of medical device manufacturing systems, ISO 13485 and FDA regulations.
- Minimum of 2 to 5 years experience in a supplier quality/supplier auditing capacity or equivalent preferred or equivalent quality function.
- Wide range of experience in different businesses: Medical Devices, Combination Devices, Pharmaceutical/API/Polymers, Calibration, Test Laboratories, Human/Animal Grafts, Injection Molding, and Packaging/Labeling (preferred)
- Strong experience with MS 365 office products.