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Quality InspectorLocation:Pompano , FLPay:–per hourDuration:Shift: Typically

Job in Pompano Beach, Broward County, Florida, 33064, USA
Listing for: inSync Staffing
Contract position
Listed on 2026-07-26
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA, Quality Engineering
Job Description & How to Apply Below
Position: Quality InspectorLocation:Pompano Beach, FLPay:$26.00–$30.00 per hourDuration:6+ Month ContractShift: Typically

Quality Inspector

We are seeking a detail-oriented Quality Inspector to join our team in Pompano Beach, FL. In this role, you will inspect raw materials, components, and finished products to ensure they meet quality standards and regulatory requirements. This is an excellent opportunity for candidates with manufacturing or medical device quality experience who thrive in a fast-paced environment.

Responsibilities
  • Inspect incoming materials, components, in-process products, and finished goods.
  • Perform visual and dimensional inspections using established procedures.
  • Compare inspection results to specifications and document nonconformances.
  • Make product accept/reject decisions based on quality standards and documented procedures.
  • Perform in-process testing and identify out-of-specification products.
  • Follow established sampling plans and Statistical Process Control (SPC) procedures.
  • Ensure proper disposition of nonconforming materials.
  • Provide technical support to Quality, Quality Engineering, and Product Support teams.
  • Train and support new employees on inspection procedures.
  • Participate in internal and external quality audits as a Subject Matter Expert (SME) for incoming inspection.
  • Support site improvement initiatives and high-priority projects.
  • Maintain a safe work environment and perform other duties as assigned.
Qualifications Required
  • High School Diploma or GED with 2+ years of related experience; or
  • Associate degree with 1+ year of related experience; or
  • Bachelor's degree; or
  • An equivalent combination of education and experience.
Preferred
  • Experience in manufacturing, medical device, or regulated industries.
  • Knowledge of 21 CFR Part 820, cGMP, and ISO 9001 standards.
  • Experience using SAP, Windchill, or other Quality Management Systems.
  • Basic Microsoft Office skills (Word, Excel, Outlook).
  • Strong attention to detail and documentation skills.
  • Excellent communication and organizational abilities.
  • Ability to work independently and collaboratively in a team environment.
  • Strong analytical and problem-solving skills.
  • Flexible and adaptable in a changing production environment.
  • Commitment to quality, safety, and continuous improvement.
Work Environment
  • Manufacturing and laboratory environment.
  • PPE required, including gloves, safety glasses, and lab coat.
  • Exposure to biological materials, including blood products.
  • Occasional gowning required.
  • Weekend work and overtime may be required.
Physical Requirements
  • Close visual acuity.
  • Occasional repetitive hand movements.
  • Lift up to 35 pounds occasionally.
  • Occasional pushing, pulling, and use of a power jack.

All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

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