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Manufacturing
Quality Inspector / Technician
New Iberia, LA

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Global Riser

Quality Assistant-Process Release

Job Description

The Quality Assistant-Process Release is based at the New Iberia onshore facility. The employee will be required to ensure that all production activities, inspections, tests, repairs, materials, equipment, and associated documentation meet internal standards, contractual requirements, customer specifications, and applicable technical regulations before final release. The role supports quality, traceability, operational safety, and compliance by reviewing technical records, identifying and resolving non-conformities, maintaining accurate quality documentation, and authorizing the release of compliant processes and equipment.
Duties:
Included, but not limited to 1. Review, check, and validate technical documents, inspection records, and evidence related to production processes. 2. Issue formal release authorizations for materials, equipment, and production stages after verifying compliance. 3. Identify non-conformities, record occurrences, and notify the responsible parties so that corrective actions are completed before release. 4. Ensure that processes comply with internal standards, customer requirements, and applicable technical standards, and other relevant requirements. 5. Organize and maintain up-to-date records of Receiving & Outgoing Inspections for internal and external audits and customer inspections. 6. Support the preparation and control of work orders, inspection reports, quality certificates, and other technical documents. 7. Monitor inspection and test results and verify that equipment complies with the established technical requirements. 8. Release equipment for use only after confirming completion of repairs and verifying both technical and documentary compliance. 9. Comply with and enforce Safety, Health, and Environmental requirements. 10. Comply with the requirements of the Company Quality Management System. 11. Comply with all Global Riser internal policies and procedures.
Experience :
Minimum:
One (1) year of experience in process control, Data Book compilation, or administrative activities within a quality function.
Desirable:
One (1) year of experience with document management systems and corporate software such as SAP, SIFAC, SharePoint, or similar systems. Skills The following are the minimum skills required to perform the function: Strong attention to detail and document accuracy. Excellent attention to detail. Good written and verbal communication with cross-functional teams. Good computer literacy. Ability to work independently and as part of a multidisciplinary team. Knowledge of manufacturing and fabrication processes. Excellent organizational and tracking skills. Problem-solving and discrepancy resolution
Qualifications Minimum:
High School Diploma or equivalent.
Preferred:
Technical Certificate in Business Administration, Manufacturing, Mechanical Technology, or a related field. Additional training in Quality Management, Document Control, and Quality Management Systems. Knowledge of applicable industry standards such as ISO 9001, API, ASME, ASTM, or other relevant industry standards. Place of work The employee will be based at the company facility in New Iberia, Louisiana. The employee will be expected to report to place of work at his/her own expense.
Benefits:
401(k) matching Paid time off Application Question(s): Are you an American Citizen by birth? What is the duration of your notice period as per your current contract? Could you please share your expected salary range for the position? Do you have at least one year of experience working in a quality, process control, document control, or similar technical/administrative function? Have you been responsible for reviewing technical documents, inspection reports, test results, or other quality records for completeness and accuracy? Have you ever been responsible for compiling or maintaining a Data Book, manufacturing record book, quality dossier, or similar technical documentation package? Have you used a document management or enterprise system such as SAP, SIFAC, SharePoint, or a similar system to track, control, or retrieve quality records? Have you ever identified a discrepancy or non-conformity in technical documentation or inspection records and formally reported it for corrective action? Have you been responsible for verifying that required inspections, tests, repairs, or other quality activities were completed before releasing equipment, materials, or a production stage? Have you worked with inspection results, certificates, test reports, work orders, or other documentation to determine whether equipment or materials met specified requirements? Have you worked with customer specifications, internal procedures, quality standards, or technical standards such as ISO 9001, API, ASME, or ASTM? Have you maintained quality records or inspection documentation in preparation for internal audits, external audits, or customer inspections? Have you worked closely with production, engineering, inspection, maintenance, or other multidisciplinary teams to resolve quality or documentation issues? Are you comfortable working independently and making a decision to hold or delay a release when required documentation, inspections, tests, or corrective actions are incomplete? Are you willing and able to work on-site at the company facility in New Iberia, Louisiana, while complying with all applicable Quality, Health, Safety, and Environmental requirements?
Work Location:
In person

Benefits

  • Paid Time Off (PTO)
  • 401(k) Plans
  • Dental Insurance