RCI-TEVA-9506 Quality Control Chemist - Cincinnati, OH

Rangam; Cincinnati (OH); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in chemical manufacturing is seeking a Quality Control Analyst I for its Cincinnati laboratory. This entry-level position involves performing quality control testing and maintaining compliance with cGMP standards. Ideal candidates will have a strong science background and laboratory experience, along with a commitment to quality and accuracy.

Qualifications

• 0-2 years of experience in a laboratory setting.
• Familiarity with Good Manufacturing Practices (GMP) preferred.
• Proficiency in analytical techniques like HPLC, GC, UV-Vis.

Responsibilities

• Perform routine analytical and microbiological testing.
• Accurately document test results and laboratory observations.
• Assist in investigation of out-of-specification results.

Skills

Attention to detail

Analytical techniques

Laboratory safety procedures

Education

Bachelor’s degree in Chemistry, Biology, Microbiology, or related life sciences

Tools

Microsoft Office

Job description

RCI-TEVA-9506 Quality Control Chemist - Cincinnati, OH

RCI-TEVA-9506 Quality Control Chemist - Cincinnati, OH

2 days ago Be among the first 25 applicants

This range is provided by Rangam. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$25.00/hr - $29.00/hr

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Position Summary:

We are seeking a detail-oriented and motivated Quality Control Analyst I to join a dynamic laboratory team. This entry-level position is responsible for performing quality control testing of raw materials, in-process samples, finished products, and stability samples in compliance with cGMP and internal standards. The ideal candidate has a strong science background, laboratory experience (academic or professional), and a commitment to quality and accuracy.

Key Responsibilities:

• Perform routine analytical and microbiological testing on various sample types using standard laboratory instrumentation and techniques (e.g., HPLC, GC, UV-Vis, pH, FTIR).
• Conduct environmental monitoring and water sampling in cleanroom and production areas as required.
• Accurately document test results and laboratory observations in accordance with Good Documentation Practices (GDP).
• Assist in investigation of out-of-specification (OOS) or atypical results by gathering data and supporting root cause analysis.
• Maintain laboratory equipment and ensure calibration and preventive maintenance are up to date.
• Follow all safety procedures and maintain a clean, organized, and compliant laboratory environment.
• Collaborate with team members and communicate test results to relevant departments.
• Participate in quality and compliance training sessions as required.

Qualifications:

• Bachelor’s degree in Chemistry, Biology, Microbiology, or a related life sciences discipline.
• 0–2 years of experience in a laboratory setting (internship, academic, or professional).
• Basic understanding of analytical techniques and laboratory safety procedures.
• Familiarity with Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs) is preferred.
• Strong attention to detail and ability to work both independently and in a team environment.
• Proficiency in Microsoft Office (Word, Excel, Outlook).

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Science

• Industries

  Chemical Manufacturing, Chemical Raw Materials Manufacturing, and Biotechnology Research

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