Quality Control Laboratory Analyst

The Procter & Gamble Company

Inwood, US
Base: $22.22ph to $29.66ph or ~$55,000pyr to ~$73,...
On-site
Good manufacturing practices (gmps)
Analytical or microbiological laboratory
Raw materials, intermediate products, finished goods analysis
Procter & Gamble is seeking a Quality Control Laboratory Analyst for their facility in Inwood, US. The role involves performing laboratory analyses in compliance with Good Manufacturing Practices (GMPs) and includes responsibilities such as testing raw materials, conducting microbiological analyses, and maintaining documentation

Job Summary

  • 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).
  • 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.
  • We do various types of work including performing raw material, finished goods, intermediate, and development sample analysis according to standard analytical procedures.

Matching Summary

Match Score: 85

Procter & Gamble is seeking a Quality Control Laboratory Analyst for their facility in Inwood, US. The role involves performing laboratory analyses in compliance with Good Manufacturing Practices (GMPs) and includes responsibilities such as testing raw materials, conducting microbiological analyses, and maintaining documentation.

Salary

Base: $22.22/hr to $29.66/hr or ~$55,000/yr to ~$73,000/yr; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Good Manufacturing Practices (GMPs)
  • analytical or microbiological laboratory
  • raw materials, intermediate products, finished goods analysis
  • routine instrument maintenance and calibration
  • cGMP principles and Good Documentation practices

Nice-to-have

  • dynamic environment
  • make a difference
  • on the floor coaching
  • problem diagnosis
  • discernment based on knowledge and experience

Key Requirements

  • 2 year degree (or more) in a Science Field
  • 5 years experience in a QC lab or GMP manufacturing operations
  • computer literacy sufficient to use standard software (MS Office)
  • experience and knowledge of basic laboratory operations
  • interpret analytical and microbiological method procedures
  • perform routine calculations pertaining to analytical chemistry
  • perform routine testing related to diluting, aliquot, and quantifying microbiological test results
  • experience resolving operational or processes failures
  • effective verbal and written communication skills
  • willing to wear appropriate safety equipment
  • work on a rotating shift schedule, including weekends
  • able to work 24/7 rotating shifts and are available for overtime and call-in as needed

Work Rights

Not specified

Tailored Resume

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