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Quality Technician-Intermediate

HonorVet Technologies

Port Allen, LA

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JOB DETAILS
SKILLS
American Society for Quality (ASQ), Analysis Skills, Analytical Chemistry, Biotech and Pharmaceutical, Calendar Management, Calibration, Certified Quality Engineer (CQE), Communication Skills, Continuous Improvement, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Data Analysis, Detail Oriented, Documentation Review, Environmental Protection Agency (EPA), FDA (Food and Drug Administration), FDA Requirements, Identify Issues, Laboratory Analysis, Laboratory Operations, Laboratory Testing, Maintain Compliance, Manufacturing, Manufacturing Operations, Materials Analysis, Mathematics, Medical Equipment, Multitasking, OSHA, Organizational Skills, Presentation/Verbal Skills, Preventative Maintenance, Printing, Process Manufacturing, Process Quality, Product Testing, Production Schedule, Production Support, Quality Assurance, Quality Control, Quality Management, Quality Metrics, Regulations, Research & Development (R&D), Support Documentation, Team Player, Technical Writing, Warehousing, Writing Skills
LOCATION
Port Allen, LA
POSTED
24 days ago
Quality Technician Intermediate
Location: Port Allen, LA 70767
Duration: 6+ months of contract
Shift: Monday Thursday, 6:00 AM 4:30 PM (Possible Tuesday Friday schedule based on production needs)


Job Summary
  • The Quality Technician will perform inspections, quality control activities, laboratory testing, and documentation review to support manufacturing and quality assurance operations.
  • This role supports production schedules, conducts investigations, monitors compliance, and ensures products meet established quality and regulatory standards.
  • Candidates may support incoming inspections, in-process inspections, or analytical laboratory functions depending on business needs.
Essential Duties and Responsibilities
Incoming Inspection & In-Process Quality Functions
  • Perform line clearances, area clearances, and in-process inspections during manufacturing operations.
  • Inspect and disposition of incoming materials and components.
  • Monitor manufacturing and warehouse operations for compliance with cGMP and quality standards.
  • Ensure non-conforming materials or products are properly identified and controlled.
  • Prepare and apply material quality status labels.
  • Verify labels after final printing activities are completed.
  • Support production schedule execution and planning activities.
  • Assist with development and maintenance of quality procedures, standards, and controls.
  • Participate in investigations related to deviations, non-conformances, and corrective/preventive actions (CAPA).
  • Support audits and quality assurance initiatives.
  • Perform additional quality-related assignments and special projects as needed.
Analytical Laboratory Functions
  • Perform chemical analysis of raw materials, in-process materials, finished products, validation, stability, and R&D samples.
  • Follow OSHA, EPA, FDA, and cGMP requirements during laboratory operations.
  • Handle laboratory reagents, standards, compressed gas cylinders, and sample materials safely and accurately.
  • Perform calibration and preventive maintenance of laboratory instruments and analytical equipment.
  • Review analytical data and other analysts' work for accuracy and compliance.
  • Complete laboratory documentation and maintain accurate records.
  • Perform housekeeping duties and submit HOLD alerts or work orders when required.
  • Support departmental projects and continuous improvement initiatives.
Education and Experience (Required)
  • " Associate's Degree in technical or scientific related field required
    " Bachelor's Degree (preferably in a science related field) preferred
    " Experience in a regulated work environment is preferred
    " Quality certificate preferred (ASQ CQE, CQA, etc.)
Education and Experience (Preferred)
  • Bachelor's Degree in a science-related field preferred.
  • Pharmaceutical or medical device industry experience preferred.
  • Quality certifications such as ASQ CQE, CQA, or similar preferred.
  • Experience with analytical testing, investigations, and technical writing preferred.
Skills, Knowledge, and Abilities (Required)
  • Understanding of FDA, OSHA, EPA, and cGMP regulations.
  • Strong analytical and troubleshooting abilities.
  • Excellent attention to detail and organizational skills.
  • Strong written and verbal communication skills.
  • Ability to multitask and work in a fast-paced manufacturing environment.
  • Mechanical aptitude and basic mathematical skills.
  • Ability to collaborate effectively across teams and departments.
  • Assertive approach to enforcing quality standards and procedures.
  • Basic knowledge of laboratory analyzers, inspection equipment, and quality systems.

About the Company

H

HonorVet Technologies

 Is a leading Service Disabled Veteran Owned Small Business providing IT, Telecom and Medical Staffing.

COMPANY SIZE
50 to 99 employees
INDUSTRY
Staffing/Employment Agencies
EMPLOYEE BENEFITS
401K, Employee Referral Program, Life Insurance
FOUNDED
2015
WEBSITE
http://www.honorvettech.com

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