Quality Assurance Specialist III

Position Summary:

The QA Specialist provides independent Quality support for GLP and GCLP studies by performing document review, protocol and experiment record review, data review, and quality event oversight activities. The role focuses on ensuring data integrity, traceability, and compliance with internal SOPs and applicable regulatory expectations, while maintaining strict independence from study execution.

This position includes high‑value QA activities that can be performed remotely, with controlled system access and clear separation from operational responsibilities.

Essential duties include but are not limited to:

Study-Audit Support

Support execution of internal audits by:

Create study-specific audit schedule prior to First patient-in (FIP) for study-specific audit

Create audit plan, execute, and draft the report for each scheduled audit (interim or associated with the final report) using objective, evidence-based language under QA lead oversight

Execute the audit through the review of controlled document, including:

SOP alignment

Version verification

Study governing documents (Lab manual, Project Specification Document, Data Transfer Agreement, clinical protocol)

Conduct QA review of clinical protocols, sample analysis protocols (SAP/SAR) and amendments, ensuring:

Version verification

Internal consistency

Alignment with study objectives and SOPs

Assure closure of quality events pertaining to study at the time of data reporting

Perform QA review (sampling) of experiment records / batch records, including:

Need access to LIMS/BSI and other systems hosting data source

Ensure alignment between protocol-defined activities and recorded execution

Training status of staff

Qualification status of equipment and reagents

Conduct QA review (sampling) against DTA of data tables, listings, and summaries, including:

Table-to-source traceability (raw data → output)

Internal consistency checks

Sample ID reconciliation and data alignment (BSI)

Apply data integrity (ALCOA+) principles during review of electronic data systems

Computerized Systems Audit Support

Support execution of internal audits by:

Preparing audit checklists

Compiling pre-audit document packages

Assisting with document-based audit reviews

Provide audit preparation support, including:

Evidence list preparation

Pre-audit document collection

Draft audit reports and summaries using objective, evidence-based language under QA lead oversight 

Data Integrity Assessment

Conduct data integrity audits of paper and electronic records

Evaluate:

Audit trails and metadata

System controls (e.g., access, security, validation)

Data lifecycle controls (collection, processing, reporting)

Assess compliance with:

ALCOA+ principles

21 CFR Part 11 / Annex 11 for electronic systems

Identify:

Data discrepancies, manipulation risks, or gaps

System vulnerabilities affecting data reliability

Miscellaneous:

Assist in training new and existing personnel, as needed

Participate in regulatory, notified body, and customer audits as needed

Provide back-up coverage for other Quality Specialists

Carry out other duties/projects as assigned

Qualifications:

Minimum Required:

Bachelor’s Degree or Master Degree in Life Sciences, Pharmacy, Biology, Chemistry

4 years of related experience in a life science GxP environment with CRO experience preferred

Hands-on experience with

ICH-GCP (E6 R2/R3)

FDA regulations (e.g., 21 CFR Part 11)

EMA / EU CTR / Annex 11

GxP frameworks (GCP, GMP, GLP, GCLP)

Preferred certification

ASQ Certified Quality Auditor (CQA)

ISO 9001 / ISO 13485 Lead Auditor

GxP Lead Auditor certifications (e.g., CQI/IRCA)

Clinical QA certifications (e.g., CCQAP)

Other Required:

High attention to detail

Strong written and verbal communication

Ability to meet deadlines and perform administrative functions

Data review expertise across computerized systems including LIMS

Understanding of Audit trails, metadata, and system validation

Knowledge of Computer System Validation (CSV) and Computer System Assurance (CSA)

Data governance frameworks

Must be able to interpret raw data vs reported data discrepancies

Microsoft Office suite proficiency including Office Word, Excel, PowerPoint

Ability to organize tasks, work independently and adapt to changing priorities

Ability to function independently within a minimally supervised environment with exceptional attention to detail required

Demonstrated highly developed communication skills including well-developed writing skills and verbal and interpersonal skills

Must be able to read, write, speak, fluently and comprehend the English language

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.

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