Quality Control Data Reviewer

Harrow, Inc.; Nashville (TN); On-site; USD 65,000 - 95,000; Full time

Job summary

Harrow, Inc. is seeking a Quality Control Data Reviewer to ensure data integrity and compliance across QC laboratory operations. The role performs second-person review of chromatographic data and reports, ensuring adherence to validated methods and cGMP requirements.

Ideal candidates bring a BS in a life sciences field and 4–5 years of lab experience, with familiarity in Chromeleon, HPLC, GC, and FTIR. Strong writing and communication skills are essential for documenting findings and supporting

Qualifications

• BS in Chemistry, Biology, Pharmaceutical or related sciences (minimum).
• 4–5 years lab experience in pharma/chemical/food labs preferred.
• Experience with data review and quality systems (21 CFR Part 11/ GMP).
• Knowledge of USP-NF and deviation/CAPA investigations.
• Strong written and verbal communication; ability to work independently.

Responsibilities

• Review QC data and analytical reports for compliance with specs and GMP.
• Examine chromatographic data, notebooks, and results for accuracy and traceability.
• Review instrument logs for correct, contemporaneous entries and compliance.
• Verify audit trails and electronic data integrity per 21 CFR Part 11.
• Document data review findings clearly and timely; escalate issues when needed.
• Support investigations and continuous improvement of data review practices.

Skills

Attention to detail

Written communication

Independent worker

Computer literacy (Word/Excel)

Data integrity & GMP awareness

Quality systems knowledge (Veeva/etc)

Education

BS in Chemistry/ Biology/ Pharmaceutical or related sciences

Tools

Chromeleon

HPLC

GC

FTIR

Job description

Before reading the job post, we encourage you to watch this video about our company. It gives you an inside look at how we started, the team and culture that made us successful, and where we're going. It's easy to read a job post and apply, but people often wonder about the culture and whether they would fit in. If you want to call Harrow your home and genuinely want to be part of a family and something big, then we encourage you to get to know us.

Who is Harrow?

Harrow (Nasdaq: HROW) is a leading provider of ophthalmic disease management solutions in North America. Harrow is an incredible entrepreneurial company – where we celebrate the ability of every member of the Harrow Family to be the CEO of their job. Harrow’s values have driven interest over the past decade in attracting high-performing professionals in a variety of disciplines. Members of our Harrow Family often express their pride in being a part of our commitment to (1) innovation, (2) patient access to affordable medicines, and (3) our track record of having never turned down an ophthalmologist doing mission work around the world – providing free medicines in support of mission work aimed at giving or maintaining the gift of sight to those most in need. We encourage you to learn more about Harrow and its unique culture to see if you’re the right person to help contribute as we build a truly exceptional company, one we are all so proud of!

Harrow’s ophthalmic pharmaceutical portfolio is one of the most comprehensive in the industry, including:

• A broad Dry Eye Disease product line, led by VEVYE ® and bolstered by well-known adjacent ocular surface disease products such as FLAREX ® and FRESHKOTE ®
• A peri-operative Surgical product line, led by TRIESENCE ® , and BYQLOVI TM
• A Rare and Specialty product line, which includes various high-need and utility products such as ILEVRO ® , NATACYN ® , and VERKAZIA ®
• A robust internal development pipeline with multiple late-stage candidates, including MELT-300, MELT-210, H-N08, and CR-01

Job Summary

The Quality Control Data Reviewer supports Quality Control laboratory operations by making sure analytical data and reports are accurate, complete, traceable, and compliant before results are released. The role verifies that testing was performed according to validated methods, approved specifications, protocols, SOPs, and cGMP requirements. It also verifies that data meets ALCOA+ data integrity principles. The Data Reviewer performs second-person review of chromatographic and other analytical data across paper and electronic systems. They identify discrepancies, errors, and compliance risks and elevate them, and they serve as the laboratory’s subject matter expert on data review practices.

Core Responsibilities

• Review Quality Control data and analytical reports, including release testing, stability testing, and analytical method validation, for compliance with approved specifications, written procedures, GMP requirements, and applicable compendial monographs in a timely manner.
• Review chromatographic data, laboratory notebooks, associated documentation, and sample results for scientific soundness, accuracy, completeness, traceability, appropriate data interpretation, and accurate representation of the final reported results.
• Review equipment and instrument logbooks to ensure entries are accurate, complete, contemporaneous, and compliant with applicable procedures.
• Verify appropriate audit trail records as part of the data review process and assess electronic data for completeness, traceability, and compliance with applicable data integrity requirements consistent with 21 CFR Part 11
• Document and communicate data review findings, including deficiencies, discrepancies, or observations identified within analytical data, supporting documentation, or reports, in a clear, concise, and timely manner.
• Conduct and document laboratory investigations, including evaluation of data discrepancies and laboratory events, with support and oversight from the Laboratory Manager, as applicable.
• Promptly report identified non-conformances, data integrity concerns, or other potential compliance issues to Laboratory Management.
• Review and revise applicable SOPs and laboratory procedures to support continuous improvement, enhance laboratory efficiency, and ensure alignment with current laboratory practices and regulatory requirements.
• Perform document control activities supporting routine laboratory operations, including issuance and control of laboratory notebooks and logbooks, document reconciliation, archival of completed records, and maintenance of controlled laboratory documentation.
• Serve as a Subject Matter Expert (SME) for Quality Control data review processes and provide guidance and support to laboratory personnel regarding data review expectations and applicable procedures.
• Support continuous improvement of laboratory data review practices and processes while maintaining compliance with applicable GMP and data integrity requirements.
• Adhere to applicable laboratory safety requirements, OSHA regulations, and established safety procedures.
• Perform other duties and responsibilities as assigned.

Qualifications & Requirements

• Minimum BS in Chemistry, Biology, Pharmaceutical or related sciences
• At least four to five years of laboratory experience preferably in pharmaceutical, chemical or food laboratory
• Previous data review experience is preferred with Chromeleon, HPLC, GC, FTIR etc.
• Knowledge of current United States Pharmacopeia and National Formulary (USP-NF)
• Working experience in Deviations, CAPA and out-of-specification (OOS) investigations utilizing root cause analysis tools
• Basic understanding of Quality Management System i.e. Veeva
• Must be able to work independently with limited direct supervision
• Good written and verbal communication skills
• Must be computer literate, working knowledge of the basic hardware, software, internet including word and excel
• Must be able to maintain a safe working environment and follow safety procedures

Position Type

• On-Site

Travel

• Up to 10%

Voluntary Self-Identification

For government reporting purposes, we ask candidates to respond to the below self-identification survey.Completion of the form is entirely voluntary. Whatever your decision, it will not be considered in the hiringprocess or thereafter. Any information that you do provide will be recorded and maintained in aconfidential file.

As set forth in Harrow, Inc.’s Equal Employment Opportunity policy,we do not discriminate on the basis of any protected group status under any applicable law.

If you believe you belong to any of the categories of protected veterans listed below, please indicate by making the appropriate selection.As a government contractor subject to the Vietnam Era Veterans Readjustment Assistance Act (VEVRAA), we request this information in order to measurethe effectiveness of the outreach and positive recruitment efforts we undertake pursuant to VEVRAA. Classification of protected categoriesis as follows:

A "disabled veteran" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service-connected disability.

A "recently separated veteran" means any veteran during the three-year period beginning on the date of such veteran's discharge or release from active duty in the U.S. military, ground, naval, or air service.

An "active duty wartime or campaign badge veteran" means a veteran who served on active duty in the U.S. military, ground, naval or air service during a war, or in a campaign or expedition for which a campaign badge has been authorized under the laws administered by the Department of Defense.

An "Armed forces service medal veteran" means a veteran who, while serving on active duty in the U.S. military, ground, naval or air service, participated in a United States military operation for which an Armed Forces service medal was awarded pursuant to Executive Order 12985.