Associate Director, DCM, Enterprise Data Quality

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

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 BMS 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.

Furthermore, this role oversees timely remediation of data issues thoroughly and effectively in a timely manner. Effective communication is key across a multi-functional team consisting of Business, IT, and Business Insights (BI)/Analytics.

Knowledge of DAMA, DCAM, and ALCOA principles is preferred.

Strong hands-on experience in data quality management, data profiling, data quality tools, and remediation process. Proven ability to interpret and implement business rules into instructions used to customize Informatica IDQ tool.

Detailed description:

-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 data quality dimensions and activities including business rules, data issues intake, data quality maturity assessment; documentation and catalog of data validations.

-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.

-Perform data quality capability and issue assessment on data sets or report then effectively review with reporting teams, IT operations, IT developers, and business unit stakeholders.

-Maintain effective communication with stakeholders to collect new Data Issues & Remediation plans. Assess remediation activities for thoroughness and document observations and recommendations.

-Follow Standard Operating Procedures (SOPs) and industry best practices to deliver on above deliverables.

Required Experience:

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

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

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

-4 to 6 years of functional knowledge of 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.

-Strong verbal and written communication skills. Ability to write clear and technically sound documentation for enterprise use.

-2 to 3 years of experience with JIRA, SharePoint, SQL, MS Excel, and Tableau is preferred.

-Experience in application development lifecycle. Experience with implementation or migration of data for enterprise-wide systems.

-Excellent oral and written communication skills in English. Strong expertise and ability to facilitate and accurately capture communication of team members.

-Ability to effectively represent data quality to produce project work independently from high-level directions.

-Demonstrate the ability to influence others to achieve objectives and effectively communicate challenging goals & objectives.

-Demonstrate strong leadership with ability to drive work forward, multi-task, make and act on decisions while balancing speed, quality, and risk.

-Able to provide innovative ideas to improve quality and compliance that create value including seeking new information and external insights.

-Excellent interpersonal skills, including written and verbal communication.

-Strong sense of ethics, diplomacy and discretion.

-Commitment to Quality.

-Strong critical thinking to analyze complex situations and discern critical issues.

-Able to work effectively in highly-matrixed and multi-cultural workforce and build strong relationships by being transparent, reliable and delivering on commitments.

-Excellent team player attitude.

-Able to manage competing priorities.

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

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