QC Laboratory Analyst

About the Role Join P&G at the Brown Summit Plant as a QC Laboratory Analyst. You will help ensure product quality and compliance with GMP, GLP, and cGMP standards through analytical testing, data recording, and collaboration with manufacturing teams. What You'll Do

• Perform raw material, finished goods, intermediate, and development sample analysis according to standard analytical procedures.
• Conduct routine instrument maintenance and calibration as needed during analytical work.
• Perform limited instrument troubleshooting and problem diagnosis.
• Assess the accuracy and reliability of analytical results, report discrepancies to supervisor.
• Conduct analytical method development work with direct supervision and mentorship from the Lab Coordinator or other staff members.
• Sample and label materials as needed per written procedures; inspect empty bulk trucks prior to loading and monitor appearance of raw materials during unloading as needed.
• Coordinate the work with the Production Lead on night and weekend shifts to ensure appropriate prioritization of work. What We're Looking For
• Education: 2-year degree or higher in a science field; commensurate experience of 5 years in a QC lab or GMP manufacturing operations.
• Computer literacy with MS Office; ability to learn specific software and instrumentation.
• Experience with 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.
• 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 with supervisor, other employees, and departments.
• Willingness to wear safety equipment (safety shoes, hearing protection, eye protection).
• Willingness to work on a rotating shift schedule, including weekends; able to work 24/7 rotating shifts and overtime/call-in as needed. Nice to Have
• Experience writing SOPs, delivering training, performing system health assessments, on-the-floor coaching, and participating in quality system investigations.
• Experience with GMP documentation and Good Documentation Practices. Compensation & Benefits
• Starting Pay / Salary Range: $24.64 - $28.56 per hour.
• Total rewards include salary, bonus (if applicable), and benefits. Your recruiter may share more about the total rewards and location-specific details during the hiring process.