Merative

A data and software partner for health and government social services, with tech and expertise to drive real progress.

Senior Director, Data Quality, Compliance, Documentation

ComplianceComplianceFull TimeRemoteTeam 1,001-5,000Since 2022H1B SponsorCompany SiteLinkedIn

Location

United States

Posted

53 days ago

Salary

$171.8K - $257.7K / year

Bachelor Degree10 yrs expEnglish

Job Description

• Oversee the creation, governance, and maintenance of all product, operational, and compliance related materials. • Implement a scalable strategy ensuring accuracy, consistency, version control, and accessibility across teams. • Standardize templates, processes, and tools to support internal operations and customer-facing content. • Ensure product, processes, and delivery align with regulatory requirements and support product adoption, regulatory & client audits, and client quality & compliance needs. • Lead the development and execution of Zelta’s quality management strategy, aligning it to organizational goals and regulatory expectations. • Establish and evolve quality processes, including audits, CAPA, SOPs, and quality metrics. • Create and maintain compliance frameworks in alignment with GxP , FDA/EMA regulations, ISO standards, and other relevant guidelines. • Conduct ongoing analysis of regulatory changes and market dynamics to ensure Zelta remains audit-ready and future-proof. • Implement clear goals, KPIs, and accountability structures to drive operational excellence. • Partner with cross-functional leaders to embed quality, compliance, and best practices throughout the organization. • Work closely with Product and Engineering to ensure new product releases meet quality and compliance standards, supported by robust documentation. • Partner with Operations and Customer Success to ensure quality and compliance programs support client satisfaction and readiness for audits or regulatory submissions. • Collaborate with Finance and the GM to ensure the quality and compliance roadmap aligns with business priorities and resource planning. • Establish scalable systems for product lifecycle management, compliance tracking, and quality reporting. • Implement continuous improvement programs to enhance process efficiency, reduce risk, and improve product and operational quality. • Serve as a subject-matter expert and spokesperson for quality and compliance matters internally and externally.

Job Requirements

  • Minimum of 10 years of progressive experience in quality, compliance, or regulatory operations within life sciences or healthcare technology.
  • Deep understanding of clinical development, GxP, and regulatory frameworks relevant to digital clinical platforms.
  • Proven experience building and scaling quality and compliance programs in complex, high-growth environments.
  • Demonstrated ability to lead teams, establish processes, and implement metrics-driven quality and compliance systems.
  • Strong orientation toward operational excellence, risk management, and continuous improvement.
  • Executive presence and strong communication skills, with the ability to influence cross-functional leaders and external stakeholders.
  • Experience working in matrixed organizations, ideally with private equity ownership or accelerated growth expectations.
  • Track record of building high-performance teams and fostering a culture of accountability, engagement, and transparency.
  • Ability to balance regulatory rigor with business goals, supporting product innovation while ensuring compliance.

Benefits

  • Remote first / work from home culture
  • Flexible vacation to help you rest, recharge, and connect with loved ones
  • Paid leave benefits
  • Health, dental, and vision insurance
  • 401k retirement savings plan
  • Infertility benefits
  • Tuition reimbursement, life insurance, EAP – and more!

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