Job Description

Kelly Outsourcing Consulting Group Kelly OCG, a managed solution provider and business unit of Kelly Services, Inc., is currently seeking a QA Associate for an engagement at one of our clients in Gurnee, IL. This role is a full-time, fully benefited position. As a Kelly OCG employee you will be eligible for Medical, Dental, 401K, and a variety of other benefits to choose from. You’ll also be eligible for paid time off, including holiday, vacation, and sick/personal time. All Kelly OCG employees receive annual performance review

Shift: M-F 8am-5ppm

Pay: $80,000-$100,000, depending on experience

Contract Length: 3-6 months

Objective:

To ensure full GMP compliance by drafting missing documentation, updating existing documentation to address gaps, conducting internal audits, managing supplier programs, handling training, performing mock recalls, and resolving backlog of customer complaints.

Responsibilities:

• Develop and update method validation protocols and reports.

• Create Standard Operating Procedures (SOPs) for validated methods.

• Maintain training records for personnel on specific test methods and equipment.

• Conduct installation, operational, and performance qualifications for analytical equipment, specifically FTIR (Fourier Transform Infrared) and GC-FID (Gas Chromatography with Flame Ionization Detector).

• Maintain calibration, preventive maintenance, and change control records.

• Document incidents, deviations, and corrective actions

• Perform and document validation activities for FTIR and GC-FID.

• Develop and validate methods for specific analytical purposes, including FTIR and GC-FID analyses.

• Prepare associated development reports, validation protocols, and validation reports.

Qualifications:

• Bachelor's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related field.

• Minimum of 3-5 years of experience in method validation within a GMP-regulated industry (e.g., pharmaceutical, biotechnology, or chemical).

• Hands-on experience in developing and validating analytical methods.

• Experience with analytical instrumentation such as FTIR and GC-FID.

• Strong background in drafting and updating validation documents and SOPs.

Skills:

• Strong understanding of GMP, FDA regulations, and method validation principles.

• Excellent written and verbal communication skills.

• Strong attention to detail and organizational skills.

• Proficiency with analytical software and tools.

• Ability to work independently and collaboratively in a team environment.

• Strong problem-solving and analytical skills.

If you, or someone you know would like to be considered for this opportunity, please apply online today to discuss the next steps.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

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