PS - Plant Quality Control - Band BTA

Overview

QC Laboratory Analyst at the Tabler Station Plant. You will work in an analytical or microbiological laboratory environment that aligns with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). Responsibilities include collection, labeling, analysis, and results recording for raw materials, intermediate products, finished goods, packaging materials, and other samples. You will participate in tracking, trend analysis, and other QC activities as directed by laboratory systems.

You may also write control documents (SOPs), deliver training, perform system health assessments, provide on-the-floor coaching, and participate in quality system failure investigations while maintaining cGMP and Good Documentation practices.

• Perform laboratory testing and related QC activities for raw materials, intermediates, finished goods, and packaging materials.
• Collect, label, analyze, and record results; track trends; and report issues to supervision.
• Write, review, or update control documents such as Standard Operating Procedures (SOPs); deliver training; perform system health assessments; provide on-the-floor coaching.
• Facilitate or participate in quality system failure investigations; maintain adherence to cGMP and Good Documentation practices.
• Perform routine instrument maintenance and calibration; conduct limited troubleshooting and problem diagnosis.
• Observe and identify problems with results and communicate findings to supervisor.
• Conduct analytical method development work under direct supervision and mentorship from Lab Leadership or other staff.
• Coordinate work with Production Lead on night and weekend shifts to ensure appropriate prioritization of tasks.
• Key analytical work:
  Physical Measurements, Wet Chemistry, Chromatography (GCs and HPLCs), and Compendial Testing.
• Key microbiology work:
  Traditional Plate Testing, Rapid Micro Screening Technology, MALDI-TOF, Autoclave.

• Typically a 2-year degree (or higher) in a Science field.
• Commensurate experience of 5 years in a QC laboratory or GMP manufacturing operations will be considered.
• Computer literacy sufficient to use standard software (MS Office) and the ability to learn specific software and instrumentation.
• Experience with basic laboratory operations (weighing, titrating, preparing volumetric solutions) and interpreting analytical/microbiological procedures and safety instructions.
• Ability to perform routine calculations for analytical chemistry (e.g., dilution, concentration) and microbiological testing (diluting, aliquoting, quantifying results).
• Experience resolving operational or process failures and developing improvement plans; strong verbal and written communication with supervisors and other teams.
• Willingness to wear appropriate safety equipment (safety shoes, hearing protection, eye protection) as required.
• Ability to work rotating shifts, including weekends, with overtime and call-in as needed.

We are committed to providing equal opportunities in employment and value diversity. We do not discriminate on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Immigration sponsorship is not available for this role. See our hiring information for work authorization details. Procter & Gamble participates in E-Verify as required by law. Reasonable accommodations are available for applicants with disabilities.

Please contact us to request accommodation.

Job Schedule:

Full time

Location:

TABLER STATION PLANT