QC Data Review and Compliance Specialist jobs in United States
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Eurofins · 7 hours ago

QC Data Review and Compliance Specialist

Eurofins is an international life sciences company providing analytical testing services across multiple industries. The QC Data Review and Compliance Specialist role focuses on supporting cGMP Quality Control operations through data entry, compliance, and documentation related to DNA, mRNA, gRNA, and LNP testing.

BiotechnologyGeneticsHealth CareLife SciencePharmaceutical
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Responsibilities

Support stability evaluations and shelf-life extensions of drug substance and drug product through population of a stability database with relevant data and generation of trending charts in addition to protocol and report authoring
Support monitoring of analytical method performance through generation of trending templates, population of database with relevant method performance indicators, and generation of trending reports
Support the shipment of quality control samples and critical reagents from/to CDMOs and contract laboratories
Perform verification of data generated internally and externally in support of method qualification/validation, lot release, and stability activities
Assist in authoring and review of internal and external protocols and reports related to analytical method qualifications/validations and product stability
Support of cGMP operations, including generation of documentation in support of change controls, CAPAs, deviations, OOS, and other investigations or assay troubleshooting

Qualification

CGMP Quality ControlData reviewDocumentation skillsMicrosoft WordMicrosoft ExcelAnalytical method performanceMultitaskingSLIMVeevaJMPLIMSCell-based assaysELISAPCRData analysisOrganizational skillsTime managementCross-functional collaborationEffective communicationAttention to detail

Required

B.S. in Chemistry, Biology, or related field with 3-4 years of relevant experience
Proficiency in Microsoft Word and Excel
Strong organizational skills, attention to detail, and accuracy in documenting results
Strong time management and multitasking abilities
Ability to work independently and collaborate in a cross-functional environment
Effective communication and documentation skills

Preferred

Experience in a clinical, QC, QA, GLP- or GMP-regulated environment is preferred
Familiarity with software systems such as SLIM, Veeva, JMP, and LIMS
Familiarity with cell-based assays, ELISA, PCR, and data analysis
Authorization to work in the United States indefinitely without restriction or sponsorship

Benefits

Comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holiday
Yearly goal-based bonus & eligibility for merit-based increases

Company

Eurofins

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Eurofins provides testing and support services to the pharmaceutical, food, environmental, and consumer products industries.

Funding

Current Stage
Public Company
Total Funding
$1.05B
2025-06-26Post Ipo Debt· $586.37M
2025-03-27Post Ipo Debt· $431.4M
2021-10-22Grant· $30M

Leadership Team

C
Cara Ahern
Documentation Specialist
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Yves-Loic Martin
Board Member
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Company data provided by crunchbase