Quality Control Laboratory Analyst at Procter & Gamble Company

Greensboro, North Carolina, United States

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Manufacturing, Consumer GoodsIndustries

Requirements

2-year degree or more in a Science Field, or commensurate experience of 5 years in a QC lab or GMP manufacturing operations
Computer literacy sufficient to use standard software (MS Office) and learn specific software and instrumentation
Experience and knowledge of basic laboratory operations such as weighing, titrating, and preparing volumetric solutions
Ability to interpret analytical method procedures and safety instructions using standard chemistry terms and measures
Ability to perform routine calculations pertaining to analytical chemistry (e.g., dilution, concentration, test results)
Experience resolving operational or process failures to understand root cause and develop an improvement plan
Effective verbal and written communication skills with supervisor, other employees, and departments
Willingness to wear appropriate safety equipment (e.g., safety shoes, hearing protection, eye protection)
Ability to work on a rotating shift schedule, including weekends, 24/7 rotating shifts, overtime, and call-in as needed

Responsibilities

Collect, label, analyze, and record results for raw materials, intermediate products, finished goods, packaging materials, and other samples
Perform tracking, trend analysis, and other QC-related responsibilities as directed by laboratory systems
Write control documents like Standard Operating Procedures (SOPs)
Deliver training, perform system health assessments, on-the-floor coaching, product disposition, and facilitate/participate in quality system failure investigations
Maintain cGMP principles and Good Documentation practices
Perform raw material, finished goods, intermediate, and development sample analysis according to standard analytical procedures
Perform routine instrument maintenance and calibration during analytical work
Conduct limited instrument troubleshooting and problem diagnosis
Use discernment to assess accuracy and reliability of analytical results, observe/identify problems, and report to supervisor
Conduct analytical method development work under direct supervision and mentorship
Sample and label materials according to written procedures or instructions
Inspect empty bulk trucks prior to loading and appearance of raw materials during unloading
Coordinate work with Production Lead on night and weekend shifts for appropriate prioritization

Skills

Key technologies and capabilities for this role

GMPcGMPGLPSOPsample analysistrend analysisinstrument maintenanceinstrument calibrationanalytical method developmentquality investigations

Questions & Answers

Common questions about this position

What education or experience is required for the Quality Control Laboratory Analyst role?

A 2-year degree or more in a Science Field is required, or commensurate experience of 5 years in a QC lab or GMP manufacturing operations will be considered.

What is the salary for this position?

This information is not specified in the job description.

Where is the job located?

The job is located at the Greensboro Brown Summit Plant.

What key skills make someone a strong fit for this role?

Candidates should have computer literacy for MS Office and lab software, experience with basic laboratory operations like weighing and titrating, and the ability to interpret analytical method procedures.

What does the work environment look like for this position?

The role involves working in a manufacturing laboratory environment that follows GLP and cGMP, with meaningful work on Day 1 including sample analysis, instrument maintenance, and coordination with production leads on various shifts.