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Quality Control (QC) Analyst

The Planet Group

Aurora (OH)

On-site

USD 60,000 - 75,000

Full time

4 days ago
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Job summary

A leading company in the healthcare industry is seeking a Quality Control (QC) Analyst for a 6-month onsite contract in Aurora, OH. This role involves performing analytical testing and supporting compliance with industry standards in a laboratory environment. Ideal candidates will possess a Bachelor’s degree in a scientific discipline and have 1-3 years of laboratory experience, showcasing their skills in both chemistry and microbiology.

Benefits

Medical insurance
Vision insurance
401(k)

Qualifications

  • 1–3 years of relevant laboratory experience.
  • Strong understanding of GMP/GDP compliance.
  • Hands-on experience with wet chemistry and microbiological testing preferred.

Responsibilities

  • Conduct routine and non-routine chemistry and microbiological testing.
  • Operate laboratory instruments based on standard procedures.
  • Analyze and calculate test results, ensuring compliance with specifications.

Skills

Laboratory testing
Analytical skills
Problem-solving
Communication

Education

Bachelor’s degree in Chemistry, Biology, or Microbiology

Tools

Laboratory instruments
Microsoft Office

Job description

Direct message the job poster from The Planet Group

Passionate EHR Recruiter aligning perfect people with perfect opportunities

Our client is seeking a dedicated Quality Control (QC) Analyst to join their team on a 6-month onsite contract in Aurora, OH. This role is ideal for candidates with a Bachelor’s degree in Chemistry, Biology, or Microbiology and 1–3 years of laboratory experience. Responsibilities include performing chemistry and microbiological testing, operating lab instruments, and supporting environmental monitoring in a GMP-regulated environment. The work schedule is Monday to Friday, 3:00 PM – 11:30 PM. This is an excellent opportunity to apply your scientific expertise in a fast-paced, quality-focused setting.

Position Summary:

The Quality Control Analyst is responsible for performing testing of raw materials, in-process formulations, and finished products within a Quality Control laboratory environment. The role requires strong technical skills in chemistry and microbiology, with a focus on analytical testing to ensure compliance with established specifications and industry standards.

Key Responsibilities:

  • Conduct routine and non-routine chemistry and microbiological testing on raw materials, in-process formulations, and finished products.
  • Operate laboratory instruments and equipment such as pH meters, conductivity meters, UV spectrophotometers, Karl Fischer titrators (KF), FTIR, and perform titrations in accordance with standard procedures.
  • Interpret and follow testing procedures from compendial methods (USP, EP, BP, JP, ACS) and EXCIPACT standards.
  • Analyze and calculate test results, ensuring they meet required specifications; document findings and generate reports.
  • Review laboratory data, including water testing, environmental monitoring, and direct measure analysis.
  • Perform calibration and routine maintenance of laboratory equipment.
  • Enter test results and raw data into Laboratory Information Management Systems (LIMS).
  • Support investigations, customer complaints, and troubleshooting by performing investigative analysis as needed.
  • Carry out Environmental Monitoring duties, which include gowning into cleanroom environments and collecting air and surface samples.
  • Apply disposition labels to materials (e.g., accepted, rejected) based on test results.
  • Handle hazardous materials safely, following PPE and safety protocols.
  • Complete and review documentation for accuracy and compliance.
  • Conduct testing for USP Purified Water and Water for Injection.
  • Author, review, and update laboratory procedures and work instructions.
  • Perform aseptic microbiological testing including Bioburden, Endotoxin, DNase, RNase, Protease, and Phosphatase.
  • Prepare and dispose of microbial media in accordance with safety and procedural standards.

Required Qualifications:

  • Bachelor’s degree in a scientific discipline such as Chemistry, Biology, or Microbiology.
  • 1–3 years of relevant laboratory experience.
  • Experience with wet chemistry and microbiological testing (e.g., acid/base titrations, water content, bioburden, endotoxin) preferred.
  • Hands-on experience with laboratory instrumentation and testing procedures.
  • Strong understanding of laboratory practices, data integrity, and GMP/GDP compliance.
  • Excellent written and verbal communication skills.
  • Proficient in Microsoft Office applications (Word, Excel, PowerPoint, Access).
  • Strong analytical and problem-solving abilities.
  • Ability to work effectively both independently and as part of a team in a regulated laboratory setting.
Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Contract
Job function
  • Job function
    Analyst
  • Industries
    Hospitals and Health Care

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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