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Chromatography Data Review Jobs (NOW HIRING)

Chemist- II

West Point, PA · On-site

$72K/yr

Software & Digital Tools Required: • Microsoft Office Suite (Word, Excel, PowerPoint) for documentation, data review, and communication. Preferred: • Empower or other chromatography data systems ...

... Chromatography Data System (CDS) supporting GC, LC, ICP, and MS workflows. You will translate ... Support budgeting, forecasting, and business/operational reviews with clear, actionable insights.

... Chromatography Data System (CDS) supporting GC, LC, ICP, and MS workflows. You will translate ... Support budgeting, forecasting, and business/operational reviews with clear, actionable insights.

... Chromatography Data System (CDS) supporting GC, LC, ICP, and MS workflows. You will translate ... Support budgeting, forecasting, and business/operational reviews with clear, actionable insights.

... Chromatography Data System (CDS) supporting GC, LC, ICP, and MS workflows. You will translate ... Support budgeting, forecasting, and business/operational reviews with clear, actionable insights.

... Chromatography Data System (CDS) supporting GC, LC, ICP, and MS workflows. You will translate ... Support budgeting, forecasting, and business/operational reviews with clear, actionable insights.

Senior Research Scientist

Morton Grove, IL · On-site

$98K - $124K/yr

Experience in data review for accuracy, completeness, and compliance with cGMP expectations ... Familiarity with Chromeleon Chromatography Data Software for data acquisition, processing, and ...

Senior Research Scientist

Morton Grove, IL

$98K - $124K/yr

Experience in data review for accuracy, completeness, and compliance with cGMP expectations ... Familiarity with Chromeleon Chromatography Data Software for data acquisition, processing, and ...

... Chromatography Data System (CDS) supporting GC, LC, ICP, and MS workflows. You will translate ... Support budgeting, forecasting, and business/operational reviews with clear, actionable insights.

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Chromatography Data Review information

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$34K

$82.6K

$136K

How much do chromatography data review jobs pay per year?

As of Jun 9, 2026, the average yearly pay for chromatography data review in the United States is $82,640.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $97,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced when reviewing chromatography data, and how can they be addressed?

One common challenge in chromatography data review is identifying and resolving inconsistencies or anomalies in the raw data, such as integration errors or unexpected peaks. Reviewers must carefully assess chromatograms, verify calculations, and ensure compliance with regulatory requirements, which can be time-consuming and detail-oriented. Effective communication with analysts and cross-functional teams is essential to clarify findings and implement corrective actions. Staying up-to-date with evolving software tools and industry standards also helps streamline the review process and maintain data integrity.

What is chromatography data review?

Chromatography data review is the process of examining and verifying data generated from chromatographic analyses, such as HPLC or GC, to ensure accuracy, compliance, and data integrity. This involves checking raw data, system suitability, peak integration, calculations, and adherence to regulatory guidelines. Chromatography data reviewers play a critical role in pharmaceutical and chemical laboratories by ensuring results are reliable and meet established quality standards.

What are the key skills and qualifications needed to thrive in Chromatography Data Review, and why are they important?

To thrive in Chromatography Data Review, you need a strong background in analytical chemistry, experience with chromatographic techniques (HPLC, GC), and a relevant science degree. Familiarity with laboratory information management systems (LIMS), chromatography data systems (such as Empower or ChemStation), and knowledge of regulatory guidelines like GMP or GLP are typically required. Attention to detail, critical thinking, and clear communication distinguish top performers in this role. These skills ensure accurate data interpretation, compliance with industry standards, and reliable reporting in laboratory environments.
Infographic showing various Chromatography Data Review job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 87% Full Time, 9% Part Time, and 3% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $82,640 per year, or $39.7 per hour.
Quality Control Data Review Specialist - GMP , Chromatography

Quality Control Data Review Specialist - GMP , Chromatography

Alcami Corporation

Wilmington, NC • On-site

Full-time

Posted 16 days ago


Alcami rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz


Job description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
Job Summary
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance-oriented training as necessary. The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed. Business needs and deadlines will require the employee to perform work duties outside of standard work hours on occasion.
On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 5:00pm.

Responsibilities
  • Performs detailed review and approval of all types of data and documents (e.g. protocols, reports, and test procedures).
  • Assist in maintaining process KPIs and quality matrix as required.
  • Drives alignment of the process with quality and compliance procedures.
  • Serves as an effective member of the Laboratory Operations team and may serve as a mentor to other employees in the area of expertise.
  • Performs floor inspections with focus on audit trail review and testing process/technique scrutiny as required.
  • Provides support to release of materials (e.g. media, reagents) as required.
  • Assists with continued improvement initiatives as needed.
  • Assists with development/writing of SOPs, Work Instructions, and other documents and/or reports as needed.
  • Complies with company polices and SOPs.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Other duties as assigned.

Qualifications
  • Bachelor's degree in Chemistry, Biology, or related field with 2+ years GMP related experience; OR Master's degree in related field with 1+ years related experience; OR equivalent education and work experience.
  • Preference to those with Bachelor's degree in Chemistry, Biology, or related field with 5+ years GMP related experience; OR Master's degree in related field with 4+ years related experience; OR equivalent education and work experience.
  • Chromatography experience required.
  • Method validation experience preferred.

Knowledge, Skills, and Abilities
  • Strong knowledge of regulations and SOPs applicable to area of responsibility and keeps abreast of new regulations and regulatory guidance in areas of expertise.
  • Excellent written and oral communication skills.
  • Good math skills.
  • Ability to be trained and to mentor others.
  • Ability to act independently.
  • Ability to interact well with employees at all levels.
  • Ability to host audits.
  • Proficiency with Microsoft Office products.

Travel Expectations
  • Up to 5% domestic travel.

Physical Demands and Work Environment
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to stand. The employee is occasionally required to walk; sit and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts and risk of electrical shock, burn hazards and microbial contamination. The employee is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.