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Data Quality Specialist

  • Location: New Brunswick
  • Job Type:Contract

Posted 26 days ago

  • Expiry Date: 07 July 2022
  • Referral: 209830@accuick.com

 Job Description:

  • This role will focus on the facilitation and execution of data quality (DQ) assessment and issue remediation activities for enterprise systems, GxP and non-GXP, and Client data analytics functions.

  • This role will be accountable for ensuring the required activities are complete according to the Enterprise Systems DQ and Issue Remediation standards. 

  • Perform the Data Quality Profiling and Assessment to identify anomalies and data quality issues/gaps that require remediation in the form of technical and/or procedural controls.

  • Create standard template for business rules; then collect, document and catalog the rules.

  • Ability to develop business rules in IDQ is preferred.

  • Maintain close and effective communication with stakeholders and team members to keep apprised of Data Issue Management & Remediation (IMR) needs. Perform data analysis, interpretation of DQ requirements, data issue and root cause analysis on authoritative systems of records and insights.

  • Perform data quality assessment to evaluate data quality maturity and capability per function or domain.

  • Experience in Risk Assessments techniques such as Failure Mode & Effects Analysis (FMEA) is a plus.

Key Competency Requirements:

  • 4-6 years of experience in Pharmaceutical/Biotech industry supporting system validation, data quality management in both GxP regulated and non-GxP environments.

  • 4-6 years of experience in data analysis, data profiling and data quality management.

  • 2-4 years of experience with Informatica Data quality (IDQ) and Axon tools.

  • Cross-functional experience with enterprise-level applications in areas such as Research, Analytical/QC, QA, Engineering, Manufacturing, Regulatory, and IT is desired.

  • Good understanding of the drug and device development process from discovery through to regulatory filing and approval of drug applications as well as commercial manufacturing processes.

  • Able to write clear and technically sound GxP regulated documentation able to satisfy quality assurance expectations and audits/inspections.

  • Advanced knowledge of SQL, MS Excel and Visio.

  • Experience with implementation or migration of data for enterprise-wide system implementation.

  • Experience with JIRA and SharePoint.

  • Experience in application development lifecycle.

About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities.

ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

Contact:

Full Name: Minal Mishra    

Email IDminalm@askconsulting.com

Phone: 470-730-2305