Regulatory Submissions Data Lead - Power Platform

Merck

Rahway (NJ)

Hybrid

USD 110,000 - 140,000

Full time

2 days ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Benefits offered by this job

Hybrid working model
Pension and health insurance
Internal reward system
5 weeks annual leave
Up-to-date laptop

Job summary

Merck is seeking a Senior Specialist in Submission Planning & Requirements Management to enhance data quality, reporting, and tool development within GRACS. This role focuses on Power Platform solutions, reporting analytics, and collaboration with stakeholders to ensure high‑quality data for downstream consumers.

You will develop Power Apps, Power Automate and Dataverse solutions, build Power BI dashboards, and drive data quality initiatives across cross‑functional teams in a regulated

Qualifications

  • Bachelor’s degree.
  • Hands-on experience with the Microsoft Power Platform (Power Apps, Power Automate, Dataverse).
  • Experience developing reports and dashboards in Power BI.
  • Strong data analysis skills.
  • Experience supporting stakeholder engagement, including requirements gathering and issue troubleshooting.
  • Ability to work across teams in a regulated, matrixed environment.

Responsibilities

  • Support data quality management and reporting, including identification, analysis, and resolution of data quality issues.
  • Develop and maintain Power Platform solutions to support submission planning, forecasting, and demand management.
  • Build and maintain Power BI reports and dashboards, providing actionable insights to planners, leadership, and downstream data consumers.
  • Extract and prepare datasets in support of analysis, reporting, and data quality initiatives.
  • Support data migration activities, including validation, reconciliation, and stakeholder issue resolution.
  • Launch and manage data quality initiatives, engaging SME stakeholders for review, validation, and continuous improvement.
  • Troubleshoot and resolve issues related to existing tools and datasets, working closely with key stakeholders.
  • Partner with submission planners and cross‑functional teams to understand requirements and translate them into scalable data and reporting solutions.

Skills

Dashboard reporting
Data analysis tools
Data extraction
Data management
Data quality assurance
Data quality control
Data reconciliation
Data reporting
Detail-oriented
Drug regulatory affairs
Pharmaceutical regulatory affairs
Project management
Quality reporting
Regulatory affairs management
Regulatory compliance
Regulatory documents
Regulatory operations
Regulatory processes
Regulatory strategy development
Regulatory submissions
Reporting tools

Job description

Merck is seeking a Senior Specialist in Submission Planning & Requirements Management to enhance data quality, reporting, and tool development within GRACS. This role focuses on Power Platform solutions, reporting analytics, and collaboration with stakeholders to ensure high‑quality data for downstream consumers.

You will develop Power Apps, Power Automate and Dataverse solutions, build Power BI dashboards, and drive data quality initiatives across cross‑functional teams in a regulated

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Regulatory Data & Submissions Specialist
Senior Regulatory Data & Submissions Specialist

Merck & Co. • Upper Gwynedd Township

Hybrid
USD 90,000 - 130,000
Hybrid work model
Pension and health insurance
5 weeks annual leave
+3
Senior Regulatory Data & Reporting Specialist
Senior Regulatory Data & Reporting Specialist

Merck • Upper Gwynedd Township

Hybrid
USD 90,000 - 120,000
Hybrid work model
Pension and health insurance
5 weeks annual leave
+1
Senior Specialist, Regulatory Submissions & Power Platform
Senior Specialist, Regulatory Submissions & Power Platform

Merck & Co. • Rahway (NJ)

Hybrid
USD 110,000 - 140,000
Hybrid work model
Pension and health insurance
Referral program
+2
Reporting and Solutions - Senior Specialist, Regulatory Affairs
Reporting and Solutions - Senior Specialist, Regulatory Affairs

Merck & Co. • Rahway (NJ)

Hybrid
USD 110,000 - 140,000
Hybrid work model
Pension and health insurance
Referral program
+2
Reporting and Solutions - Senior Specialist, Regulatory Affairs
Reporting and Solutions - Senior Specialist, Regulatory Affairs

Merck & Co. • Upper Gwynedd Township

Hybrid
USD 90,000 - 130,000
Hybrid work model
Pension and health insurance
5 weeks annual leave
+3
Reporting and Solutions - Senior Specialist, Regulatory Affairs
Reporting and Solutions - Senior Specialist, Regulatory Affairs

Merck • Upper Gwynedd Township

Hybrid
USD 90,000 - 120,000
Hybrid work model
Pension and health insurance
5 weeks annual leave
+1
Reporting and Solutions - Senior Specialist, Regulatory Affairs
Reporting and Solutions - Senior Specialist, Regulatory Affairs

Merck • Rahway (NJ)

Hybrid
USD 110,000 - 140,000
Hybrid working model
Pension and health insurance
Internal reward system
+2
Associate Director, Regulatory Affairs - Power Platform Solutions Specialist
Associate Director, Regulatory Affairs - Power Platform Solutions Specialist

Merck • Rahway (NJ)

On-site
USD 140,000 - 170,000
Hybrid work setup
Associate Director, Regulatory Affairs - Power Platform Solutions Specialist
Associate Director, Regulatory Affairs - Power Platform Solutions Specialist

Merck • North Wales

On-site
USD 140,000 - 190,000
Hybrid work
Travel opportunities (approx. 10%)
Associate Director, Regulatory Affairs — Power Platform Lead
Associate Director, Regulatory Affairs — Power Platform Lead

Merck • North Wales

Hybrid
USD 140,000 - 190,000
Hybrid work
Travel opportunities (approx. 10%)