×
Register Here to Apply for Jobs or Post Jobs. X

Quality Technician

Job in Port Allen, West Baton Rouge Parish, Louisiana, 70767, USA
Listing for: neteffects
Full Time position
Listed on 2026-03-07
Job specializations:
  • Manufacturing / Production
    Quality Engineering
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Control / Manager
Salary/Wage Range or Industry Benchmark: 25 - 27.19 USD Hourly USD 25.00 27.19 HOUR
Job Description & How to Apply Below
Location: Port Allen

Quality Technician

Pay: $25.00 – $27.19/hr, paid weekly
Schedule: Monday – Thursday, 6:00 AM – 4:30 PM
Potential future schedule: Tuesday – Friday based on production needs.
Possible 2nd shift: 12:00 PM – 10:00 PM (Mon–Thu) with $2/hr shift differential
.

Location: Port Allen, LA 70767
Duration: 6-month contract

Summary

This role is essentially a quality inspector on a pharmaceutical manufacturing floor who checks materials, monitors production, verifies labeling, and ensures compliance with FDA and cGMP regulations.

Full Summary

The Quality Technician ensures manufacturing, packaging, and handling of pharmaceutical and medical device products meet current Good Manufacturing Practices (cGMP) and regulatory standards. This role performs inspections, monitors production quality, and verifies materials to ensure products meet safety and quality requirements.

Key Responsibilities
  • Perform line clearances, in-process inspections, and incoming material inspections.
  • Monitor manufacturing and warehouse activities for compliance with quality and regulatory standards.
  • Label materials and verify accuracy of all product labels after printing.
  • Monitor production processes and support statistical process control (SPC/SQC) activities.
  • Control and document non-conforming materials, components, or equipment.
  • Assist with quality procedures, audits, investigations, and corrective actions.
  • Support production schedules and participate in quality-related improvement projects.
Required Skills
  • Knowledge of cGMP, FDA, OSHA, and EPA regulations in pharmaceutical or medical device manufacturing.
  • Proficiency with Microsoft Word and Excel.
  • Strong attention to detail and organizational skills.
  • Basic math skills and mechanical aptitude.
  • Ability to communicate effectively and collaborate across departments.
  • Basic understanding of laboratory analyzers and inspection equipment.
Education & Experience
  • Associate’s degree in a technical or scientific field required.
  • Bachelor’s degree in a science-related field preferred.
  • Experience in a regulated manufacturing or laboratory environment preferred.
  • Quality certification (ASQ CQE, CQA, or similar) preferred.
Benefits (employee contribution)
  • Health insurance
  • Health savings account
  • Dental insurance
  • Vision insurance
  • Flexible spending accounts
  • Life insurance
  • Retirement plan

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. Rate of pay within the stated range will depend on the qualification of the applicant.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary