QC Data Reviewer II – Analytical Chemistry

Curia Aalborg ApS; City of Rensselaer (NY); On-site; USD 73,000 - 93,000; Full time

Benefits offered by this job

Generous benefits

Paid training

Career advancement

Education reimbursement

401K with matching

Learning platform

Job summary

Curia seeks a Data Reviewer II in Rensselaer, NY to perform rigorous data reviews of analytical outputs from GC, HPLC/UHPLC, IR, DSC, UV-Vis and more. You will verify traceability, calibration status, and compliance with GDP procedures while supporting QA initiatives and client methods.

The role requires a Bachelor’s in natural science or pharmacy and 3–5 years in QC in a GMP/GLP environment, with strong communication and problem-solving skills.

Qualifications

• Bachelor's degree in natural science or pharmacy and 3–5 years in QC or related industry.
• Experience in cGMP or GLP pharmaceutical environments is required.
• Strong data review, accuracy and data integrity focus.

Responsibilities

• Perform technical review of analytical data from GC, HPLC/ UHPLC, IR, DSC, UV-Vis, and related methods.
• Verify data traceability, logbooks, calibrations, and stock of standards/reagents.
• Ensure cGMP compliance and assist QA initiatives as needed.
• Provide training and escalation of OOS to QC/QA leadership.
• Enter data into stability summaries and prepare data summaries for management.

Skills

Data review

cGMP

Instrument interpretation

Attention to detail

Written/verbal communication

Education

Bachelor's Degree in Natural Science or Pharmacy

3–5 years QC experience

Experience in GLP/good laboratory practices

Tools

GC

HPLC/UHPLC

IR

DSC

UV-Vis

Karl Fischer

Job description

Curia seeks a Data Reviewer II in Rensselaer, NY to perform rigorous data reviews of analytical outputs from GC, HPLC/UHPLC, IR, DSC, UV-Vis and more. You will verify traceability, calibration status, and compliance with GDP procedures while supporting QA initiatives and client methods.

The role requires a Bachelor’s in natural science or pharmacy and 3–5 years in QC in a GMP/GLP environment, with strong communication and problem-solving skills.