Analytical Data Review Associate

Piper Companies; Durham (NC); On-site; USD 48,000 - 58,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401K

Sick leave

Job summary

Piper Companies seeks an Analytical Data Review Associate for a 6-month onsite contract in Durham, NC. The role focuses on verifying laboratory data, reviewing chromatographic results, and ensuring ALCOA+ data integrity in a GMP-regulated setting.

The ideal candidate has hands-on experience with Waters Empower and a strong quality/compliance mindset, with availability for a first-shift, on-site schedule.

Qualifications

• Bachelor's degree in a related scientific field.
• Experience reviewing laboratory/analytical data in a regulated pharma/biotech environment.
• Experience with Waters Empower and data integrity practices.

Responsibilities

• Examine lab records and test results to verify accuracy and completeness.
• Review chromatographic data using Waters Empower to ensure data integrity.
• Evaluate HPLC results, chromatograms, and supporting records for analytical validity.
• Collaborate with scientists and QA to resolve data discrepancies and compliance findings.
• Support microbiology operations with additional data review as needed.

Skills

GMP/GLP knowledge

ALCOA+ data integrity

Attention to detail

Strong communication

Education

Bachelor's degree in Microbiology/related field

Tools

Waters Empower software

Electronic chromatographic data systems

Job description

Piper Companies is seeking an experienced Analytical Data Review Associate to support a leading biopharmaceutical manufacturing environment in Durham, North Carolina. This Analytical Data Review Associate opportunity is a 6-month contract position working fully onsite during first shift, Monday through Friday. The ideal candidate will bring a strong background in laboratory data verification, chromatographic data assessment, and regulatory compliance within a GMP-regulated setting.

Responsibilities

• Examine laboratory-generated records, test results, and analytical documentation to verify accuracy, completeness, and adherence to established quality requirements.
• Perform detailed reviews of chromatographic data utilizing Waters Empower, ensuring data integrity and compliance with regulatory expectations.
• Evaluate HPLC results, chromatograms, calculations, and supporting records to confirm analytical validity and identify potential inconsistencies.
• Partner with laboratory scientists and quality personnel to resolve data discrepancies, documentation concerns, and compliance-related findings.
• Support microbiology operations while providing additional analytical or formulation sciences data review assistance as required.

Qualifications

• Bachelor's degree in Microbiology, Biological Sciences, Chemistry, Pharmaceutical Sciences, or a related scientific field.
• Prior experience reviewing laboratory or analytical data within a regulated pharmaceutical, biotechnology, CRO, or laboratory environment.
• Strong hands‑on expertise with Waters Empower software and electronic chromatographic data systems.
• Demonstrated ability to interpret HPLC data, chromatograms, analytical reports, and associated laboratory documentation.
• Working knowledge of GMP, GLP, ALCOA+ principles, and data integrity requirements, coupled with exceptional attention to detail and strong communication skills.

Compensation

Salary Range: $35.00 - $42.00 per hour

Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

Application Details

Location: Durham, NC

Schedule: Monday - Friday | First Shift | Fully Onsite

Employment Type: 6-Month Contract

Posted Date: October 26, 2026

Apply By: November 26, 2026

Keywords

Analytical Data Review, Data Integrity, Waters Empower, Empower Software, HPLC, Chromatography, Analytical Chemistry, GMP, GLP, ALCOA+, Pharmaceutical Manufacturing, Biotechnology, Quality Assurance, Quality Control, Laboratory Documentation, Analytical Testing, Microbiology, Formulation Sciences, Chromatograms, Method Review, Compliance, Regulated Environment, Batch Records, Laboratory Investigations, CAPA, Analytical Reports, Validation, Laboratory Operations, Scientific Data Review, Audit Readiness, SOP Compliance, Electronic Data Systems, Biopharmaceutical, QC Laboratory, Deviations, Root Cause Analysis, Data Verification, Pharmaceutical Quality, Research Associate, Durham NC

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