Quality Control Laboratory Analyst

Procter & Gamble • Inwood, NY

175d • $22 - $29

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 who 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 Tabler Station Plant. As a QC Laboratory Analyst, you could work in an analytical or microbiological 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. In addition to laboratory testing, QC Analysts may be required to write control documents like Standard Operating Procedures (SOPs), deliver training, perform system health assessments, carry out “on the floor” coaching, facilitate or participate in quality system failure investigations. Maintain cGMP principles and Good Documentation practices. Where do you fit in? Meaningful work on Day 1 We do various types of work including performing raw material, finished goods, intermediate, and development sample analysis according to standard analytical procedures. We perform routine instrument maintenance and calibration as needed during analytical work. We conduct limited instrument troubleshooting and problem diagnosis. We use discernment based on knowledge and experience as to the accuracy and reliability of analytical results. You will observe and identify problems with results and report to your supervisor. You will conduct analytical method development work with direct supervision and mentorship from Lab Leadership or other staff members. You may sample and label materials as needed according to written procedures or specific instructions, inspect appearance of raw materials during unloading as needed. Another responsibility will include coordinating the 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.
• Have computer literacy sufficient to use standard software (MS Office) as well as the ability to learn specific software and instrumentation.
• Possess experience and knowledge of basic laboratory operations such as weighing, titrating, and preparing volumetric solutions.
• Interpret analytical and microbiological method procedures and safety instructions using standard scientific terms and measures.
• Perform routine calculations pertaining to analytical chemistry (e.g. dilution, concentration, test results).
• Perform routine testing related to diluting, aliquot, and quantifying microbiological test results.
• Have experience resolving operational or processes failures to understand root cause and able to develop an improvement plan.
• Have effective verbal and written communication skills with supervisor, other employees, and departments.
• Willing to wear appropriate safety equipment, such as safety shoes, hearing protection, and eye protection, wherever these things are necessary.
• Able to work 24/7 rotating shifts and are available for overtime and call-in as needed.

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 supervisor.
• Conduct analytical method development work with direct supervision and mentorship.
• Sample and label materials according to written procedures or specific instructions.
• Inspect appearance of raw materials during unloading as needed.
• Coordinate work with the Production Lead on night and weekend shifts.

Benefits

• Salary range of $22.22/hr to $29.66/hr or ~$55,000/yr to ~$73,000/yr with built in overtime.
• Potential opportunity to earn up to $42.08/hr or ~$103,000/yr with built in overtime as you grow in the organization.
• Total rewards at P&G include salary + bonus (if applicable) + benefits.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree
• Number of Employees: 1,001-5,000 employees