Quality Inspector in Largo
Energy Jobline ZR, Largo, FL, United States
Quality Inspector – 3rd Shift
Schedule:
2nd Shift
3:00 PM - 11:30 PM, Monday–Friday
3rd Shift:
11:00 PM - 7:30 AM, Monday–Friday
Training:
First 3 weeks on 1st shift ( 7:00 AM - 3:30 PM )
Position Summary
We are seeking experienced Quality Inspectors to support our 3rd shift manufacturing operations. This role is responsible for ensuring product quality and compliance with regulatory and customer requirements in a regulated manufacturing environment.
Key Responsibilities
Perform quality inspections and product evaluations in compliance with established procedures
Ensure compliance with
ISO 9001, ISO 13485, FDA 21 CFR 820 , and related regulatory standards
Process, investigate, and document product nonconformances
Support first article inspections, qualifications, and process validation activities
Interpret and apply engineering drawings and specifications
Utilize basic inspection and measuring tools including micrometers, calipers, torque testers, thread gauges, go
o-go gauges, gauge blocks, and scales
Maintain accurate records and controlled documentation within electronic document control systems
Follow written procedures, work instructions, drawings, and forms
Prioritize work effectively while adapting to changing production needs
Collaborate respectfully and professionally with team members
Comply with all company policies, safety rules, lean initiatives, and regulatory requirements
Maintain regular, reliable, and punctual attendance
Perform other duties as assigned
Required Qualifications
Minimum 3 years of experience in a regulated manufacturing environment
Experience in plastic injection molding, medical device manufacturing, or component manufacturing
Hands‑on experience with product quality compliance requirements
Experience in high-volume manufacturing and/or assembly environments
Ability to manage multiple priorities and projects
Strong attention to detail and documentation accuracy
Proficiency with Microsoft Office
High School Diploma required
Prior Quality Inspector experience in a cGMP and ISO 13485 environment
IQMS software knowledge highly desirable
Work Environment & Dress Code
Clean, climate-controlled (A/C) manufacturing environment
Closed-toe shoes, jeans, and t-shirt required
Hair and beard nets may be required
Ideal Candidate Traits
Strong work ethic
Interested in long-term growth with the company
Detail-oriented with a slow, steady, and consistent work pace
Low-key, quiet, and focused demeanor
#J-18808-Ljbffr
Schedule:
2nd Shift
3:00 PM - 11:30 PM, Monday–Friday
3rd Shift:
11:00 PM - 7:30 AM, Monday–Friday
Training:
First 3 weeks on 1st shift ( 7:00 AM - 3:30 PM )
Position Summary
We are seeking experienced Quality Inspectors to support our 3rd shift manufacturing operations. This role is responsible for ensuring product quality and compliance with regulatory and customer requirements in a regulated manufacturing environment.
Key Responsibilities
Perform quality inspections and product evaluations in compliance with established procedures
Ensure compliance with
ISO 9001, ISO 13485, FDA 21 CFR 820 , and related regulatory standards
Process, investigate, and document product nonconformances
Support first article inspections, qualifications, and process validation activities
Interpret and apply engineering drawings and specifications
Utilize basic inspection and measuring tools including micrometers, calipers, torque testers, thread gauges, go
o-go gauges, gauge blocks, and scales
Maintain accurate records and controlled documentation within electronic document control systems
Follow written procedures, work instructions, drawings, and forms
Prioritize work effectively while adapting to changing production needs
Collaborate respectfully and professionally with team members
Comply with all company policies, safety rules, lean initiatives, and regulatory requirements
Maintain regular, reliable, and punctual attendance
Perform other duties as assigned
Required Qualifications
Minimum 3 years of experience in a regulated manufacturing environment
Experience in plastic injection molding, medical device manufacturing, or component manufacturing
Hands‑on experience with product quality compliance requirements
Experience in high-volume manufacturing and/or assembly environments
Ability to manage multiple priorities and projects
Strong attention to detail and documentation accuracy
Proficiency with Microsoft Office
High School Diploma required
Prior Quality Inspector experience in a cGMP and ISO 13485 environment
IQMS software knowledge highly desirable
Work Environment & Dress Code
Clean, climate-controlled (A/C) manufacturing environment
Closed-toe shoes, jeans, and t-shirt required
Hair and beard nets may be required
Ideal Candidate Traits
Strong work ethic
Interested in long-term growth with the company
Detail-oriented with a slow, steady, and consistent work pace
Low-key, quiet, and focused demeanor
#J-18808-Ljbffr