Quality Control Analyst – Lab Testing & Compliance

Automatic Data Processing, Inc.

Aguadilla (PR)

On-site

USD 42,000 - 56,000

Full time

2 days ago
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Job summary

Automatic Data Processing, Inc. is seeking a Technical Associate – QC in Aguadilla, PR for rigorous quality control testing and data analysis to ensure product integrity. You will document results, maintain audit-ready records, and collaborate with cross-functional teams to resolve deviations and drive process improvements.

The role emphasizes GLP/SOP familiarity, analytical proficiency, and effective communication to support regulatory compliance and high-quality outcomes.

Qualifications

  • Bachelor's degree in Chemistry, Biology, Biochemistry, or related field.
  • Experience in quality control or laboratory environment.
  • Familiarity with GLP and SOPs.
  • Strong analytical skills and proficiency with laboratory instrumentation and software.
  • Excellent written and verbal communication skills.

Responsibilities

  • Perform routine and non-routine quality control tests on raw materials, in-process samples, and finished products according to established protocols.
  • Document and analyze test results accurately, maintaining detailed records to support compliance and audit readiness.
  • Identify deviations or non-conformances and communicate findings promptly to the quality management team for corrective action.
  • Maintain laboratory equipment and ensure calibration and maintenance schedules are followed to guarantee reliable test results.
  • Collaborate with production, research, and quality assurance teams to support investigations and implement process improvements.

Skills

Analytical skills
Written & verbal communication
Documentation

Education

Bachelor's degree in Chemistry, Biology, Biochemistry

Tools

Laboratory instrumentation
Laboratory software

Job description

Automatic Data Processing, Inc. is seeking a Technical Associate – QC in Aguadilla, PR for rigorous quality control testing and data analysis to ensure product integrity. You will document results, maintain audit-ready records, and collaborate with cross-functional teams to resolve deviations and drive process improvements.

The role emphasizes GLP/SOP familiarity, analytical proficiency, and effective communication to support regulatory compliance and high-quality outcomes.

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