Quality Lab Technician - Mon-Thu, 10-Hour Onsite Role

Avadim Holdings, Inc

Swannanoa (NC)

On-site

USD 40,000 - 60,000

Full time

14 days+
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Job summary

Avadim Holdings, Inc is seeking a Quality Lab Technician in Swannanoa, North Carolina. The role involves performing both routine and non-routine laboratory tests while ensuring compliance with FDA guidelines. Key responsibilities include sample collection, data recording, and equipment maintenance. Candidates must possess strong communication skills and attention to detail, and preferred knowledge of FDA Drug Manufacturing Regulations. The position offers a structured onsite work schedule from Monday to Thursday, totaling 40 hours per week.

Qualifications

  • Knowledge of FDA Drug Manufacturing Regulations preferred.
  • Working knowledge of MS Office Suite and database systems.
  • Ability to work autonomously and under pressure.
  • Excellent verbal and written communication skills.
  • Keen attention to detail.

Responsibilities

  • Collect, receive, label, and/or analyze samples.
  • Execute testing according to standard operating procedures.
  • Record all experimental data and test results accurately.
  • Ensure safety guidelines are adhered to at all times.
  • Complete documentation according to FDA guidelines.
  • Clean and maintain laboratory equipment.
  • Review production records for accuracy.
  • Input data in inventory control software.
  • Complete invoice reconciliation for outsourced testing.

Skills

Knowledge of FDA Drug Manufacturing Regulations
Working knowledge of MS Office Suite
Ability to work autonomously
Excellent verbal and written communication skills
Keen attention to detail

Job description

Avadim Holdings, Inc is seeking a Quality Lab Technician in Swannanoa, North Carolina. The role involves performing both routine and non-routine laboratory tests while ensuring compliance with FDA guidelines. Key responsibilities include sample collection, data recording, and equipment maintenance. Candidates must possess strong communication skills and attention to detail, and preferred knowledge of FDA Drug Manufacturing Regulations. The position offers a structured onsite work schedule from Monday to Thursday, totaling 40 hours per week.
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