Senior Quality Control Analyst I - Data Review

Tandym-Group; Woburn (MA); On-site; USD 55,000 - 69,000; Full time

Job summary

Tandym-Group in Woburn, MA is seeking a Senior Quality Control Analyst I for data review. The role focuses on reviewing analytical data, ensuring compliance, and supporting timely product release decisions in a gene therapy context.

The position requires review of cGMP data packages, collaboration with internal and external labs, and strong knowledge of ALCOA+ and FDA data integrity guidance. In-person, day shift, Monday–Friday.

Qualifications

• 5+ years of experience in a GMP/GLP environment.
• Bachelor's or master's degree in Cell Biology, Molecular Biology, Biochemistry, or related field.
• Strong experience reviewing analytical data from molecular biology, bioassay, biochemical, or microbiological testing.
• Thorough understanding of cGMP regulations, FDA data integrity guidance, ALCOA+ principles, and quality systems.
• Excellent attention to detail, problem-solving, communication, and organizational skills.

Responsibilities

• Review and approve cGMP analytical data packages generated by internal and external laboratories.
• Verify analytical data for accuracy, completeness, compliance, and alignment with approved methods and regulatory requirements.
• Examine raw data, electronic records, calculations, chromatograms, and worksheets.
• Assess data integrity, audit trail compliance, and adherence to ALCOA+ principles.
• Collaborate with internal teams and external laboratories to resolve data discrepancies and support product release activities.

Skills

Data integrity

cGMP compliance

Analytical data review

FDA regulations

ALCOA+ principles

Quality systems

Education

Bachelor's or Master's in Cell Biology, Molecular Biology, Biochemistry, or related field

Tools

LIMS

ELN

Empower

SoftMax Pro

JMP

BioRad QuantaSoft

Job description

Senior Quality Control Analyst I - Data Review (CR/512372) Woburn, Massachusetts

Salary: USD40 - USD50 per hour

A biotech organization in Massachusetts is seeking a Senior Quality Control Analyst I for a data review role. This position supports gene therapy quality control activities by reviewing analytical data, ensuring compliance, and helping maintain the integrity and timeliness of product release decisions.

About the Opportunity:

• Shift: Day


• Schedule: Monday to Friday


• Hours: Standard business


• Setting: In-person

Responsibilities:

• Review and approve cGMP analytical data packages generated by internal and external laboratories


• Verify analytical data for accuracy, completeness, compliance, and alignment with approved methods and regulatory requirements


• Examine raw data, electronic records, calculations, chromatograms, and worksheets


• Assess data integrity, audit trail compliance, and adherence to ALCOA+ principles


• Collaborate with internal teams and external laboratories to resolve data discrepancies and support product release activities

Qualifications:

• 5+ years of industry experience in a GMP or GLP environment


• Bachelor's or master's degree in Cell Biology, Molecular Biology, Biochemistry, or a related field


• Strong experience reviewing analytical data from molecular biology, bioassay, biochemical, or microbiological testing


• Thorough understanding of cGMP regulations, FDA data integrity guidance, ALCOA+ principles, and quality systems


• Excellent attention to detail, problem-solving, communication, and organizational skills

Desired Skills:

• Experience with qPCR, ddPCR, ELISA, cell-based assays, HPLC, electrophoresis, or similar analytical platforms


• Familiarity with LIMS, ELN, Empower, SoftMax Pro, JMP, BioRad QuantaSoft, or comparable tools


• Experience supporting deviations, investigations, CAPAs, OOS, OOTs, change controls, audits, inspections, SOPs, or procedure updates