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Qa Shop Inspector Jobs (NOW HIRING)

Legend Biotech USA, Inc.

Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the floor ... Support regulatory inspections and audits as needed.Consistently perform tasks in adherence with ...

Legend Biotech USA, Inc.

Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the floor ... Support regulatory inspections and audits as needed.Consistently perform tasks in adherence with ...

DEMGY PACIFIC

QA Inspector

Tacoma, WA

$22 - $27/hr

QUALITY ASSURANCE INSPECTOR REPORTS TO: QUALITY CONTROL SUPERVISOR DIRECT REPORTS: N/A POSITION ... Ability to inspect molded parts utilizing conventional machine shop inspection tools

Barfield Inc

Quality Inspector

Atlanta, GA · On-site

The Shop Inspector will support our Quality Control department. Position: Inspector Department: Quality Control FLSA status: Full time-Non-Exempt General: To make sure the shop complies with all ...

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Qa Shop Inspector information

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How much do qa shop inspector jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for qa shop inspector in the United States is $20.39, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $23.08 per hour, depending on experience, location, and employer.

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For Qa Shop Inspector jobs, the most frequently searched job titles are:

Manager, Quality Assurance Shop Floor - Summit West NJ

Summit, NJ • On-site

Veteran Jobs - 2023 Mar 01 - Veterans Resources
Technology, Communication and Media • 11 - 50 employees
Learn more about Veteran Jobs - 2023 Mar 01 - Veterans Resourcesexternal

Full-time

Posted 18 days ago

Job description

 

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is On-Site at the location detailed in the job post.
Position Summary
The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, Label Operations and Warehouse Operations. 
This position will oversee and partner with operational areas, to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP. 
This position is a people manager position, leading a team of individual contributors in the Quality Assurance Shop Floor Organization.
Wednesday to Saturday - 12-hour shift (every other Wed off) 
5 a.m. to 5:30 p.m.
Duties/Responsibilities
Oversee performance of QA shop floor activities. 
Supervise Quality Assurance Shop Floor employees. 
Regularly spend time coaching and mentoring operators and QA personnel while on the manufacturing floor. Provide guidance and training on quality programs. 
Lead Quality on-the-floor oversight to Manufacturing/QC/Warehouse/ Packout operations/Label Operations. Proactively identify risks/critical issues and drive mitigations and escalate to management as needed.
Develop, review and/or approve temporary and non-routine procedure for event response.  
Periodically observe operations. Proactively identify risks and drive improvements. 
Provide quality oversight to non-routine maintenance work. Review and approve return to service plans. 
Coordinate and lead area walkthroughs to identify quality issues. Negotiate remediations and drive alignment of implementation plans. 
Act as a QA subject matter expert on behalf of the facility during audits and inspections.
Ensure manufacturing compliance with applicable procedures and batch records. 
Perform review of operational documentation including manufacturing batch records. 
Must have strong authorship and ability to critically review investigations, interpret results and generate technical conclusions consistent with Quality risk management principles. 
Must be skilled in planning and organizing, decision-making, and building relationships. 
Knowledge of quality processes, including material disposition, change control, product complaints, deviations, investigations, and CAPA management. 
For markets requiring an Authorized Person (AP) release to be performed by Summit, act as designated AP performing Certification/Release for Supply in accordance with the PIC/S Guide to GMP (including Annex 16) and any local market requirements e.g. Australian Therapeutic Goods Administration (TGA) requirements, including the Therapeutic Goods Act 1989 and associated GMP principles.
Perform verification and reconciliation of issued drug product labels.

     

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