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Quality Lab Associate I

Kelly • Round Lake, IL 60073 • Posted 2 days ago via LinkedIn

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In-person • Full-time • $25.00-$27.50/hr • Entry Level

Job Highlights

Using AI ⚡ to summarize the original job post

The Quality Lab Associate I at Kelly in Round Lake, IL, is responsible for conducting biological, chemical, and physical analyses on pharmaceutical products throughout all stages of the manufacturing process. This includes analyses on raw materials, initial, in-process, and final products, and environmental monitoring programs. The role operates under minimal supervision and requires working weekend shifts to support training and projects. Candidates must not be allergic to Penicillin or Cephalosporin.

Responsibilities

  • Conduct critical chemical and physical analyses on Raw Materials, Initial, In-process and Final products, and samples collected from environmental monitoring programs in the company’s manufacturing facilities.
  • Use sophisticated laboratory instrumentation (HPLC, FTIR, UV, GC etc) and computer systems to collect and record data.
  • Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles.
  • Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
  • Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
  • Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.
  • Perform equipment maintenance and calibrations as required.
  • Document the completion of testing in Notebooks, Controlled documents, Forms and LIMS and maintain accurate and complete quality records.
  • Follow, understand and comply with company’s SOP’s and policies on cGMP’s and safety. Maintain a clean, safe and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas.
  • Investigate deviations and write exception/OOL/OOS/OOT documents.
  • Support improvement projects and drive efficiency through utilization of LEAN management principles (i.e., 6S, Kaizens etc).
  • Proactively and cooperatively communicate with peers and management to ensure awareness of progress and issues; recommend solutions when issues arise.
  • Maintain and meet the highest standards in quality, customer service and regulatory compliance.
  • Other projects as assigned.

Qualifications

Required

  • Bachelor’s degree in Chemistry or Science related degree with 6 months or more of experience
  • Must not be allergic to Penicillin and Cephalosporin or their related products and/or materials
  • Ability to lift up to 50 pound when required
  • Occasional weekend work required
  • Must be able to distinguish between colors

Preferred

  • Knowledge of Empower CDS and LIMS
  • Knowledge of GLP, cGMP requirements and familiar with USP/ICH guidelines
  • Excellent communication (oral and written) and interpersonal skills
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude in a highly dynamic environment

About Kelly

Kelly Services, Inc. operates in the staffing industry, providing temporary and contract staffing, direct-hire opportunities, outsourcing, and consulting services across various sectors. The company, founded in 1946, has a global presence in over 40 countries and caters to businesses of all sizes, assisting them in meeting their workforce goals effectively.

Full Job Description

Kelly is hiring a Quality Lab Associate I at one of our premiere clients in Round Lake, IL.


Pay: $25/hr - $27.50/hr

Shift: Weekend + 2 other nights

Hours: 4 10-hour shifts (Friday through Sunday 10 pm to 8:30 am and then two nights of their choice for the 40 hours.)

Assignment Length: 7.5 months


Summary:

  • The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs.This is a third shift position but will be required to work on weekends to support training of analysts and to support projects and/or production, as required.
  • A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials.


Essential Duties and Responsibilities:

  • Conduct critical chemical and physical analyses on Raw Materials, Initial, In-process and Final products, and samples collected from environmental monitoring programs in the company’s manufacturing facilities. Work under minimum supervision.
  • Use sophisticated laboratory instrumentation (HPLC, FTIR, UV, GC etc) and computer systems to collect and record data.
  • Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles.
  • Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
  • Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
  • Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.
  • Perform equipment maintenance and calibrations as required.
  • Document the completion of testing in Notebooks, Controlled documents, Forms and LIMS and maintain accurate and complete quality records.
  • Follow, understand and comply with company’s SOP’s and policies on cGMP’s and safety. Maintain a clean, safe and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas.
  • Investigate deviations and write exception/OOL/OOS/OOT documents.
  • Support improvement projects and drive efficiency through utilization of LEAN management principles (i/e/ 6S, Kaizens etc).
  • Proactively and cooperatively communicate with peers and management to ensure awareness of progress and issues; recommend solutions when issues arise.
  • Maintain and meet the highest standards in quality, customer service and regulatory compliance.
  • Other projects as assigned.


Qualifications:

  • Knowledge of Empower CDS and LIMS is preferred but not required
  • Knowledge of GLP, cGMP requirements and familiar with USP/ICH guidelines is preferred but not required
  • Excellent communication (oral and written) and interpersonal skills
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude in a highly dynamic environment
  • Ability to lift up to 50 pound when required
  • Occasional weekend work required
  • Must be able to distinguish between colors.


Education and/or Experience:

  • Bachelor’s degree in Chemistry or Science related degree with 6 months or more of experience