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Quality Consultant II (Knowledge of Medical Device )

Job Description

Title:                      Quality Consultant II

Location:              Neenah ,WI ,54956

Duration:             4 Months


Job Requirements


Position Purpose
:

Provides Quality/Regulatory support for Post Market Surveillance team while ensuring compliance to established procedures and processes – including complaint handling and adverse event reporting.

General Expectations and Accountabilities:

1)    Demonstrate safety as a value by performing all job functions safely, while also complying with corporate policies and departmental procedures, in an effort to reduce risk and eliminate loss.

2)    Manages self in accordance with the expected behaviors of the Leadership Qualities.

3)    Ensures activities and items are in compliance with both company quality assurance standards and applicable government regulations, such as GMPs and ISO requirements.

4)    Maintain and demonstrate an appropriate level of knowledge and skill in quality systems, processes, and regulations.

5)    Establish and maintain good customer rapport.  Develop and maintain a strong spirit of partnership.

6)    Conduct all communications and transactions with the utmost integrity. Communicate fully with superiors, teammates, and others who have a need to know.

7)    Capability in Quality Management Systems, ISO, and GMPs to support activities.




Position Specific Accountabilities
:

1)    Executes assigned Post-Market Surveillance activities, including Complaint Assessment, Investigation, Trending/Reporting, Final Review, Sample Evaluation, and Flow to Work to assist others as needed.

2)    Perform Decision Tree Determination and drafting of adverse event reports for regulatory. 

3)    Achieves and maintains required competence level for Medical Device Reporting.

4)    Maintains relationships with Consumer Services, including reporting of errors, troubleshooting, and coordinating complaint handling activities and improvements.

5)    Helps execute CAPAs and QNCs.

6)    Complies with QMS, ISO, FDA GMP's, and Health Canada requirements.

7)    Provides Post-Market Surveillance support to Mills and/or Product Forms via Standard Work, data analysis, and communication.  




Scope

This position reports to KCNA Senior Quality Manager – QMS and Post-Market Surveillance. Has responsibility for execution of and record-keeping for quality systems in support of regulated products. Carries out routine workload and small system improvement projects with minimal direction, but asks for assistance/guidance when appropriate.




Qualifications/Education/Experience Required
:

Normally requires a Bachelor’s degree in science, engineering or related discipline and/or 5+ years broad experience in Complaint Handling/Post Market-Surveillance or related filed.  Knowledge of Medical Device requirements (e.g. ISO13485, 21 CFR 820 and 21 CFR 803) is preferred.



Job Snapshot

Location US-WI-Neenah
Employment Type Full-Time
Pay Type Year
Pay Rate N/A
Store Type
Apply

Company Overview

American Cybersystems, Inc. (ACS Group)

ACS Group provides services to Fortune 1000 companies across various industry verticals. With a proven track record of managing project demands while improving the efficiency, productivity and profitability of new and existing projects through process improvement, ACS Group is consistently recognized for identifying and implementing strategic solutions that create and preserve long-term business value. Learn More

Contact Information

US-WI-Neenah
Kumudani Joshi
678-207-5202
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Snapshot
American Cybersystems, Inc. (ACS Group)
Company:
US-WI-Neenah
Location:
Full-Time
Employment Type:
Year
Pay Type:
N/A
Pay Rate:
Store Type:

Job Description

Title:                      Quality Consultant II

Location:              Neenah ,WI ,54956

Duration:             4 Months


Job Requirements


Position Purpose
:

Provides Quality/Regulatory support for Post Market Surveillance team while ensuring compliance to established procedures and processes – including complaint handling and adverse event reporting.

General Expectations and Accountabilities:

1)    Demonstrate safety as a value by performing all job functions safely, while also complying with corporate policies and departmental procedures, in an effort to reduce risk and eliminate loss.

2)    Manages self in accordance with the expected behaviors of the Leadership Qualities.

3)    Ensures activities and items are in compliance with both company quality assurance standards and applicable government regulations, such as GMPs and ISO requirements.

4)    Maintain and demonstrate an appropriate level of knowledge and skill in quality systems, processes, and regulations.

5)    Establish and maintain good customer rapport.  Develop and maintain a strong spirit of partnership.

6)    Conduct all communications and transactions with the utmost integrity. Communicate fully with superiors, teammates, and others who have a need to know.

7)    Capability in Quality Management Systems, ISO, and GMPs to support activities.




Position Specific Accountabilities
:

1)    Executes assigned Post-Market Surveillance activities, including Complaint Assessment, Investigation, Trending/Reporting, Final Review, Sample Evaluation, and Flow to Work to assist others as needed.

2)    Perform Decision Tree Determination and drafting of adverse event reports for regulatory. 

3)    Achieves and maintains required competence level for Medical Device Reporting.

4)    Maintains relationships with Consumer Services, including reporting of errors, troubleshooting, and coordinating complaint handling activities and improvements.

5)    Helps execute CAPAs and QNCs.

6)    Complies with QMS, ISO, FDA GMP's, and Health Canada requirements.

7)    Provides Post-Market Surveillance support to Mills and/or Product Forms via Standard Work, data analysis, and communication.  




Scope

This position reports to KCNA Senior Quality Manager – QMS and Post-Market Surveillance. Has responsibility for execution of and record-keeping for quality systems in support of regulated products. Carries out routine workload and small system improvement projects with minimal direction, but asks for assistance/guidance when appropriate.




Qualifications/Education/Experience Required
:

Normally requires a Bachelor’s degree in science, engineering or related discipline and/or 5+ years broad experience in Complaint Handling/Post Market-Surveillance or related filed.  Knowledge of Medical Device requirements (e.g. ISO13485, 21 CFR 820 and 21 CFR 803) is preferred.



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