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Quality Control Inspector I

In Ohio / United States

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Quality Control Inspector I   

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JOB TITLE:

Quality Control Inspector I

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

Lockbourne Ohio / United States

JOB DESCRIPTION:

Job Description:

1st Shift
Work Hours
7:00 AM-3:30 PM

In this role, you have the opportunity to perform independent activities that support the execution of regulatory/quality management system requirements related to the management of nonconforming material, incoming inspection and final release acceptance activities for medical devices, consumer goods, or other products within warehouse and distribution facilities.

You are responsible for:

• Follow assigned procedures and complete all training records.
• QN management (creation, processing, and closure)
• Ensure quality system records (NCM and other applicable records) are complete, accurate and comply with procedures.
• Execute delivery holds
• Partner with warehouse and factory teams
• Perform incoming inspection and/or final release acceptance activities within warehouse and distribution facilities.
• Understand device history records and Bill of Materials (BOM)
• Partner with warehouse operations, Supplier Quality, on resolving quality issues.
• Ensure quality system records (DHR, inspection, and other applicable records) are complete, accurate and comply with procedures
• Meet departmental metrics
• Manage inspection plans and their maintenance per engineering change requests
• Support first article inspection process for purchased finished goods


To succeed in this role, you should have the following skills and experience:
High School Diploma or equivalent required, Bachelor’s degree in business, engineering, or other related field preferred.
• Support lean initiatives and contributes to continuous improvement and complete QEKs.
• Demonstrated proficiency in reading, math, written skills, and manual dexterity, required.
• Ability to communicate clearly, both verbally and in writing, required.
• Strong attention to detail, time management, organization, and communication skills, required
• Prior experience in working in a manufacturing or warehouse related environment.
• Understanding of CAPA, as well as global medical device regulations, requirements and standards such as 21 CFR Parts 803, 806, and 820, ISO13485, and EU MDR.



Experience: 2 years of experience in position or specialization. Education: High-school/Associates or equivalent experience if applicable. Certification if applicable. Discuss inspection results with those responsible for products, and recommend necessary corrective actions.  Discard or reject products, materials, and equipment not meeting specifications.  Inspect, test, and sample materials or assembled parts or products for defects and deviations from specifications.  Observe and monitor production operations and equipment to ensure conformance to specifications and make or order necessary process or assembly adjustments.

Position Details

POSTED:

May 12, 2022

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S16475580076259

LOCATION:

Ohio / United States

CITY:

Lockbourne

Job Origin:

Jobsrus_organic_feed

A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Quality Control Inspector I    Apply

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Job Description:

1st Shift
Work Hours
7:00 AM-3:30 PM

In this role, you have the opportunity to perform independent activities that support the execution of regulatory/quality management system requirements related to the management of nonconforming material, incoming inspection and final release acceptance activities for medical devices, consumer goods, or other products within warehouse and distribution facilities.

You are responsible for:

• Follow assigned procedures and complete all training records.
• QN management (creation, processing, and closure)
• Ensure quality system records (NCM and other applicable records) are complete, accurate and comply with procedures.
• Execute delivery holds
• Partner with warehouse and factory teams
• Perform incoming inspection and/or final release acceptance activities within warehouse and distribution facilities.
• Understand device history records and Bill of Materials (BOM)
• Partner with warehouse operations, Supplier Quality, on resolving quality issues.
• Ensure quality system records (DHR, inspection, and other applicable records) are complete, accurate and comply with procedures
• Meet departmental metrics
• Manage inspection plans and their maintenance per engineering change requests
• Support first article inspection process for purchased finished goods


To succeed in this role, you should have the following skills and experience:
High School Diploma or equivalent required, Bachelor’s degree in business, engineering, or other related field preferred.
• Support lean initiatives and contributes to continuous improvement and complete QEKs.
• Demonstrated proficiency in reading, math, written skills, and manual dexterity, required.
• Ability to communicate clearly, both verbally and in writing, required.
• Strong attention to detail, time management, organization, and communication skills, required
• Prior experience in working in a manufacturing or warehouse related environment.
• Understanding of CAPA, as well as global medical device regulations, requirements and standards such as 21 CFR Parts 803, 806, and 820, ISO13485, and EU MDR.



Experience: 2 years of experience in position or specialization. Education: High-school/Associates or equivalent experience if applicable. Certification if applicable. Discuss inspection results with those responsible for products, and recommend necessary corrective actions.  Discard or reject products, materials, and equipment not meeting specifications.  Inspect, test, and sample materials or assembled parts or products for defects and deviations from specifications.  Observe and monitor production operations and equipment to ensure conformance to specifications and make or order necessary process or assembly adjustments.


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