Unclassified - Browns Summit, NC

posted 5 months ago

Full-time - Entry Level
Browns Summit, NC

About the position

Do you have a passion for working in a laboratory? Do you thrive in a dynamic environment? We're looking for great teammates that have these qualities and want to make a difference by cultivating good manufacturing practices (GMPs) and company quality principles to deliver the product performance and quality for the consumers P&G serves. We have several types of Quality Control roles available at our Brown Summit Plant. As a QC Laboratory Analyst, you could work in a manufacturing laboratory environment that stays in sync with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). The work will require collection, labeling, analysis, and results recording related to raw materials, intermediate products, finished goods, packaging materials and other samples. Tracking, trend analysis, and other Quality Control (QC) related responsibilities will be performed as directed by laboratory systems. We also have roles for a QC Analyst that require writing control documents like Standards Operating Procedures (SOPs), delivering training, performing system health assessments, on-the-floor coaching, product disposition, and facilitating or participating in quality system failures investigations. Maintaining cGMP principles and Good Documentation practices is essential. Meaningful work starts on Day 1. We perform various types of work including performing raw material, finished goods, intermediate, and development sample analysis according to standard analytical procedures. We conduct routine instrument maintenance and calibration as needed during analytical work. We also conduct limited instrument troubleshooting and problem diagnosis. You will use discernment based on knowledge and experience as to the accuracy and reliability of analytical results. Observing and identifying problems with results and reporting to your supervisor is a key responsibility. You will conduct analytical method development work with direct supervision and mentorship from the Lab Coordinator or other staff members. Sampling and labeling materials according to written procedures or specific instructions, inspecting empty bulk trucks prior to loading, and the appearance of raw materials during unloading as needed are also part of the role. Another responsibility will include coordinating the work with the Production Lead on night and weekend shifts to ensure appropriate prioritization of work.

Responsibilities

  • 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.
  • Observe and identify problems with results and report to the supervisor.
  • Conduct analytical method development work with direct supervision and mentorship.
  • Sample and label materials according to written procedures or specific instructions.
  • Inspect empty bulk trucks prior to loading and the appearance of raw materials during unloading as needed.
  • Coordinate work with the Production Lead on night and weekend shifts to ensure appropriate prioritization of work.

Requirements

  • Have a 2 year degree or more in a Science Field.
  • Commensurate experience of 5 years in a QC lab 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 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.
  • 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, such as safety shoes, hearing protection, and eye protection.

Nice-to-haves

  • Experience in a laboratory environment with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP).
  • Ability to work on a rotating shift schedule, including weekends.
  • Availability for overtime and call-in as needed.

Benefits

  • Health savings account
  • Health insurance
  • Dental insurance
  • 401(k)
  • Paid time off
  • Parental leave
  • Vision insurance
  • Employee discount
  • Safety equipment provided
  • Life insurance
  • Paid sick time
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