Full-Time

Director CMC Operations Content Management and Digital Enablement

Regulatory Affairs-CMC

Posted on 9/11/2026

Deadline 9/26/26
Merck

Merck

10,001+ employees

Pharmaceutical company developing medicines and vaccines

Compensation Overview

$173.2k - $272.6k/yr

+ Annual bonus + Long-term incentive

No H1B Sponsorship

North Wales, PA, USA + 1 more

More locations: Rahway, NJ, USA

Hybrid

Hybrid work arrangement; no relocation support is provided.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Power BI
Data Visualization

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Requirements
  • A bachelor's degree is required; an advanced degree in Life Sciences, Regulatory Affairs, Information Systems, or a related field is preferred.
  • Extensive experience in content management, regulatory operations, or pharmaceutical operations, with strong emphasis on CMC content processes.
  • Demonstrated experience leading content management strategy, governance, or process improvement initiatives.
  • Experience with digital transformation, system implementation, or content platform optimization.
  • Strong communication, influence, and stakeholder management skills.
  • Ability to work effectively across complex global and cross-functional environments.
  • Strong expertise in several of the following: regulatory content management; structured content and modular authoring; metadata and taxonomy governance; document lifecycle management; global submission support processes; operational process design and continuous improvement; and digital enablement strategies.
  • Experience with Veeva Vault, Lorenz docuBridge, and Microsoft Power BI.
  • Knowledge of strategic thinking and business acumen, executive presence and influence, content management and operational leadership, change management and organizational leadership, cross-functional collaboration, innovation and continuous improvement, operational excellence, talent development and mentorship, and analytical and problem-solving capabilities.
  • Business process improvement, change management, compliance remediation, cross-functional project management, data reporting, document control systems, employee training programs, executive leadership, executive presence, high-performance team building, influencing, innovation, negotiation, organizational capability, organizational leadership, people leadership, policy implementation, prioritization, process improvement, regulatory affairs management, regulatory submissions, stakeholder management, strategic leadership, and strategic thinking.
Responsibilities
  • Define and lead the CMC content management strategy across the content lifecycle.
  • Establish governance, standards, and operating procedures for content creation, review, approval, reuse, maintenance, archiving, and retrieval.
  • Serve as the enterprise subject matter expert for content management processes supporting CMC regulatory activities.
  • Drive consistent application of document standards, metadata, taxonomy, and version control practices.
  • Ensure content management processes support compliance, inspection readiness, and global regulatory requirements.
  • Identify and implement opportunities to improve content quality, consistency, and reuse across the organization.
  • Champion structured authoring and modular content approaches to enable more efficient content operations and future digital capabilities.
  • Develop and maintain a scalable content management operating model aligned with business needs and regulatory expectations.
  • Partner with cross-functional stakeholders to define roles, responsibilities, workflows, and governance forums.
  • Lead process improvement initiatives that reduce duplication, improve efficiency, and strengthen control.
  • Establish and monitor performance metrics related to content quality, cycle time, reuse, compliance, and operational effectiveness.
  • Support audit and inspection readiness through content governance and data integrity practices.
  • Lead the implementation, optimization, and adoption of digital tools that support content management capabilities.
  • Partner with IT and business stakeholders to define business requirements, future-state workflows, and system enhancements.
  • Evaluate and advance opportunities to leverage automation, artificial intelligence, structured content, and digital technologies to improve content operations.
  • Serve as a strategic business partner for content-related platform enhancements and digital capability roadmaps.
  • Support adoption of content management systems, document management tools, and related regulatory platforms.
  • Collaborate with CMC Regulatory Affairs and other stakeholders to ensure content management processes support submission development and lifecycle activities.
  • Align content management practices with global regulatory requirements and CMC business priorities.
  • Provide operational guidance for content-related challenges, escalations, and continuous improvement opportunities.
  • Contribute to the modernization of CMC regulatory operations through improved content processes and digital readiness.
  • Lead governance discussions, working sessions, and executive-level presentations related to content management strategy and performance.
  • Build partnerships across Regulatory Affairs, Quality, IT, Supply Chain, and external vendors.
  • Mentor and develop team members and foster accountability, innovation, and continuous improvement.
  • Define KPI frameworks for content management performance and maturity.
  • Develop reporting standards and dashboards to support data-driven decision-making.
  • Monitor content quality, reuse, compliance, cycle time, and digital adoption.
  • Present insights, trends, and recommendations to senior leadership to inform prioritization and improvement efforts.
Desired Qualifications
  • An advanced degree in Life Sciences, Regulatory Affairs, Information Systems, or a related field.
  • Independent judgment.

Merck is a global healthcare company that develops medicines, vaccines, and animal health products. It advances long-term health by conducting research and development to create new treatments for diseases such as cardiovascular disease, diabetes, and cancer, then brings these medicines to patients, healthcare professionals, and institutions worldwide. The company’s products work by undergoing scientific discovery, clinical testing, and regulatory approval before being manufactured and sold or distributed through patient assistance programs. What sets Merck apart is its large, diversified portfolio across human medicines, vaccines, and animal health, along with a strong emphasis on R&D, global reach, and support services like Merck Connect and Merck Manuals that provide professional resources. Merck’s goal is to tackle major health threats by applying science to discover and deliver therapies that improve patient outcomes and public health across the globe.

Company Size

10,001+

Company Stage

IPO

Headquarters

Kenilworth, Illinois

Founded

1891

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Simplify Jobs

Simplify's Take

What believers are saying

  • August 2026 melanoma data validated Merck's next-generation cancer franchise beyond Keytruda.
  • July 2026 Lipfendra approval opens a new cardiovascular growth market before Keytruda erosion.
  • February 2026 oncology reorganization concentrates resources ahead of patent expiry and late-stage launches.

What critics are saying

  • Keytruda loses U.S. compound patent protection in December 2028, pressuring oncology revenue.
  • Summit and Akeso's ivonescimab beat Keytruda in China lung cancer data in 2026.
  • Merck's 2025 $3 billion cost-cutting plan includes 6,000 layoffs, signaling margin strain.

What makes Merck unique

  • Keytruda remains Merck's oncology engine; July 2026 approvals expanded perioperative bladder and kidney use.
  • August 2026 Moderna partnership produced first positive Phase 3 individualized mRNA cancer vaccine results.
  • Lipfendra's July 2026 FDA approval created Merck's first oral PCSK9 inhibitor.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

401(k) Company Match

Paid Vacation

Paid Sick Leave

Hybrid Work Options

Growth & Insights and Company News

Headcount

6 month growth

-20%

1 year growth

-20%

2 year growth

-20%
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