Joulé
Job Title
Quality Associate Location
Raleigh, NC Employment Type
Contract Hours
8 AM – 5 PM, Monday – Friday Responsibilities
Lead and manage the migration of quality documents into Veeva Vault, ensuring accuracy and compliance with documentation standards. Support the transition of legacy records into Veeva, maintaining traceability and completeness. Build and maintain trackers to monitor key performance indicators (KPIs), batch record status, and release metrics. Assist in batch record reviews to ensure documentation is complete, compliant, and ready for release. Support release activities by coordinating documentation readiness and collaborating with QA team members and cross‑functional teams. Requirements
Associate degree (required); BS/BA in life sciences or closely related field (preferred). 3+ years of pharmaceutical/biotech working experience in Quality Assurance in an FDA‑regulated industry. Experience with batch record review, document control, and release processes. Familiarity with SAP inventory system. Familiarity with Veeva Vault or similar document management systems; Power BI knowledge preferred. Proficiency in Microsoft Office tools and Veeva Quality systems. Strong organization, communication, and technical writing skills. Self‑directed, goal‑oriented, and quality conscious. Ability to work cross‑functionally with QA, MSAT, QC and Supply teams. Seniority Level
Mid‑Senior level Equal Opportunity Statement
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Reference: #558-Scientific
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Quality Associate Location
Raleigh, NC Employment Type
Contract Hours
8 AM – 5 PM, Monday – Friday Responsibilities
Lead and manage the migration of quality documents into Veeva Vault, ensuring accuracy and compliance with documentation standards. Support the transition of legacy records into Veeva, maintaining traceability and completeness. Build and maintain trackers to monitor key performance indicators (KPIs), batch record status, and release metrics. Assist in batch record reviews to ensure documentation is complete, compliant, and ready for release. Support release activities by coordinating documentation readiness and collaborating with QA team members and cross‑functional teams. Requirements
Associate degree (required); BS/BA in life sciences or closely related field (preferred). 3+ years of pharmaceutical/biotech working experience in Quality Assurance in an FDA‑regulated industry. Experience with batch record review, document control, and release processes. Familiarity with SAP inventory system. Familiarity with Veeva Vault or similar document management systems; Power BI knowledge preferred. Proficiency in Microsoft Office tools and Veeva Quality systems. Strong organization, communication, and technical writing skills. Self‑directed, goal‑oriented, and quality conscious. Ability to work cross‑functionally with QA, MSAT, QC and Supply teams. Seniority Level
Mid‑Senior level Equal Opportunity Statement
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Reference: #558-Scientific
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