Analytical Chemist

Integrated Resources, Inc ( IRI ); Cincinnati (OH); On-site; USD 65,000 - 75,000; Full time

Job summary

Integrated Resources, Inc (IRI) seeks a Data Review Scientist I to review testing data across materials and products, ensuring accuracy and GMP compliance. You will verify calculations, instrument outputs, and documentation, addressing discrepancies to support timely product release.

The ideal candidate holds a Bachelor’s in a scientific field, with 2+ years in a laboratory or regulated setting, and hands-on experience with HPLC, GC, spectroscopy, and dissolution methods.

Qualifications

• Bachelor's degree in Chemistry, Biology, Biochemistry or related field.
• 2+ years of relevant experience in a laboratory/regulated environment preferred.
• Experience with laboratory data review or analytical testing preferred.
• Knowledge of GMP, Good Documentation Practices and data integrity principles.

Responsibilities

• Review analytical data, lab records and supporting documentation from QC laboratories.
• Review data from HPLC, GC, spectroscopy, dissolution testing and wet chemistry.
• Verify calculations, results, specifications, instrument outputs and chromatograms.
• Ensure records comply with approved methods, specifications, SOPs, GMP and GDP.
• Identify errors or discrepancies and work with staff to resolve.
• Review data for raw materials, in-process samples, finished products and stability studies.
• Use laboratory information systems to review and track data and sample status.
• Support investigations, deviations, OOS/OOT events and other quality activities.
• Maintain accurate and traceable records in line with data integrity expectations.
• Collaborate with QC analysts, laboratory leadership, QA and other teams to support release timelines.
• Follow safety, quality, regulatory and site procedures.

Skills

Attention to detail

Scientific judgment

Data review

Data integrity

Education

Bachelor's degree in Chemistry, Biology, Biochemistry, or related field

Tools

HPLC

GC

Spectroscopy

Dissolution testing

Wet chemistry

Job description

The Data Review Scientist I will review testing associated with raw materials, in-process samples, finished products, and stability samples. The ideal candidate will have strong attention to detail, scientific judgment, and the ability to identify and resolve data or documentation discrepancies.

Key Responsibilities

• Review analytical data, laboratory records, and supporting documentation generated by QC laboratories.
• Review data from techniques such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods.
• Verify calculations, results, specifications, instrument outputs, chromatograms, and associated documentation for accuracy and completion.
• Ensure laboratory records comply with approved methods, specifications, SOPs, GMP requirements, and Good Documentation Practices.
• Identify errors, discrepancies, atypical results, or documentation deficiencies and work with laboratory personnel to facilitate resolution.
• Review data associated with raw materials, in-process samples, finished products, and stability studies.
• Utilize laboratory information systems and other electronic systems to review and track analytical data and sample status.
• Support investigations, deviations, OOS/OOT events, and other quality activities as assigned.
• Maintain accurate and traceable records in accordance with applicable data integrity expectations.
• Collaborate with QC analysts, laboratory leadership, Quality Assurance, and other teams to support testing and product-release timelines.
• Follow applicable safety, quality, regulatory, and site procedures.

Qualifications

• Bachelor's degree in required, preferably in Chemistry, Biology, Biochemistry, or a related scientific field.
• 2+ years of relevant experience preferred, ideally in a laboratory, pharmaceutical, biotechnology, or regulated environment.
• Experience with laboratory data review or analytical laboratory testing preferred.
• Working knowledge of analytical techniques such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry.
• Knowledge of GMP regulations, Good Documentation Practices, pharmaceutical quality standards, and data integrity principles is a must.