Quality Control Technician I – Raw Materials (CPG)

Beauty Manufacturing Solutions Corp

Coppell (TX)

On-site

USD 45,000 - 65,000

Full time

6 days ago
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Job summary

Beauty Manufacturing Solutions Corp in Coppell, TX is seeking a Quality Control Technician I (Raw Materials) to sample, test, and release incoming raw materials, ensuring they meet high quality standards and regulatory requirements.

You will work cross-functionally with Production and Manufacturing, maintain detailed GMP records, and support special projects while demonstrating strong attention to detail and flexibility in schedule, including overtime and night shifts.

Qualifications

  • Detail oriented.
  • Good verbal and written communication and basic computer literacy (MS Office) required.
  • Good math proficiency and good color vision.
  • Organized and analytical, self-directed and motivated.
  • Must be able to work flexible schedules including overtime, nightshift and weekend shifts.

Responsibilities

  • Ensure SOPs are followed to meet and exceed Quality Standards set forth in Specifications.
  • Ensure team maintains highest levels of safety to build an environment where the team’s well-being is a top priority.
  • Ensure proper use of Personal Protective Equipment.
  • Collaborate and communicate with upper management and Operations team.
  • Perform sampling, testing, and release of incoming raw materials in a highly regulated environment.
  • Document all results and report all non-conformances to specification or standard.
  • Generate GMP-compliant records as required by SOPs, methods, or regulations.
  • Own and lead special projects as assigned.
  • Perform other duties as required by Quality management.

Skills

Detail oriented
Verbal & written communication
MS Office
Math proficiency
Color vision
Organized and analytical

Job description

Beauty Manufacturing Solutions Corp in Coppell, TX is seeking a Quality Control Technician I (Raw Materials) to sample, test, and release incoming raw materials, ensuring they meet high quality standards and regulatory requirements.

You will work cross-functionally with Production and Manufacturing, maintain detailed GMP records, and support special projects while demonstrating strong attention to detail and flexibility in schedule, including overtime and night shifts.

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