Integra LifeSciences

Sr. Director - IT Applications

Integra LifeSciences$192K — $263K *
Healthcare
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in IT, Engineering, or related field; Master's degree preferred.
  • At least 15 years of IT experience, with 5+ years in a director-level role in life sciences or healthcare.
  • Experience overseeing enterprise applications like QMS, Regulatory Systems, and PLM.
  • Knowledge of regulatory compliance and system validation standards.
  • Proven track record managing global support teams and vendor coordination.
  • Collaborative leadership with a focus on translating business needs into technology solutions.
  • Strong strategic thinking and execution in quality and compliance management.

Responsibilities

  • Define and implement the IT roadmap for QMS and related platforms.
  • Lead internal and external IT teams to foster accountability and excellence.
  • Advise leadership on technology solutions for Quality, Regulatory, and Operations.
  • Ensure QMS platforms meet compliance and regulatory standards.
  • Oversee regulatory systems for submissions and compliance tracking.
  • Manage PLM platforms for product data and change management.
  • Lead AMO services ensuring high availability and performance.

Benefits

  • Medical, dental, and vision insurance.
  • Life insurance and disability coverage.
  • Business accident insurance and legal assistance.
  • 401(k) savings plan options.
  • Eligible for bonus, commission, or other variable compensation.
Full Job Description
The Senior Director of IT is responsible for the strategic leadership, delivery, and operational excellence of enterprise systems supporting Quality Management Systems (QMS), Regulatory & Compliance platforms, Product Lifecycle Management (PLM), and Application Management & Operations (AMO). Quality, Regulatory & Product Systems.

The role balances strategy, governance, and hands-on execution, while ensuring systems meet global regulatory requirements and operate with high availability, security, and performance.

Key Responsibilities

IT Strategy & Leadership
  • Define and execute the IT roadmap for QMS, Regulatory, PLM, and supporting enterprise platforms aligned with business and compliance objectives.
  • Provide leadership to internal IT teams and external partners, fostering accountability, continuous improvement, and operational excellence.
  • Act as a trusted technology advisor to Quality, Regulatory, R&D, and Operations leadership.

Quality Management Systems (QMS)
  • Own IT accountability for QMS platforms supporting CAPA, Deviations, Complaints, Change Control, Audit Management, and Document Control.
  • Ensure systems are compliant with applicable regulations and standards (e.g., FDA, ISO, GxP, 21 CFR Part 11, Annex 11 where applicable).
  • Partner with Quality teams to drive standardization, process maturity, and system adoption globally.

Regulatory & Compliance Systems
  • Lead IT ownership of regulatory systems supporting submissions, registrations, labeling, and compliance tracking.
  • Ensure system validation, data integrity, audit readiness, and inspection support capabilities.
  • Manage regulatory system upgrades and enhancements with minimal disruption to compliance or business operations.

Product Lifecycle Management (PLM)
  • Oversee PLM platforms enabling product data management, design control, BOMs, change management, and traceability.
  • Integrate PLM with ERP, Manufacturing, Quality, and other enterprise systems to enable end-to-end digital product lifecycle visibility.
  • Drive simplification and harmonization of product data and processes across regions and product lines.

Application Management & Operations (AMO)
  • Lead AMO services for supported platforms, ensuring high availability, predictable performance, and strong service-level outcomes.
  • Establish and monitor KPIs for incident management, problem management, change management, and release stability.
  • Drive continuous improvement through automation, optimization, and reduction of technical debt.

Governance, Risk & Compliance
  • Ensure all systems follow IT governance, validation, cybersecurity, and data privacy standards.
  • Support audits and inspections by providing system evidence, documentation, and technical expertise.
  • Manage vendor relationships, contracts, and service delivery performance.

Financial & Delivery Management
  • Own budget planning, forecasting, and cost optimization for the application portfolio.
  • Oversee large-scale programs, system implementations, and upgrades using disciplined delivery and change management practices.


REQUIRED SKILLS & MINIMUM QUALIFICATIONS
  • Bachelor's degree in information technology, Engineering, or a related discipline required; Master's degree is highly desirable.
  • Minimum of 15 years progressive IT experience; with minimum 5 plus years of experience as a Director or Sr. Director in Life science / Healthcare industry.
  • Extensive background in overseeing enterprise applications preferably QMS, Regulatory Systems, and PLM platforms within global enterprise settings.
  • Comprehensive knowledge of regulatory compliance, system validation, and audit preparedness.
  • Proven ability to manage GCC and/or AMO models, coordinate vendors, and lead global support teams effectively.
  • A collaborative leader with a business-focused approach, adept at translating business and compliance requirements into robust, scalable technology solutions.
  • Strategic thinker demonstrating strong execution discipline and a thorough understanding of quality, compliance, and risk management.

Additional Information:
This is a hybrid role, and the ideal candidate will be based out of Princeton, NJ. The hybrid schedule requires in-office presence on Tuesdays, Wednesdays, and Thursdays, with the option to work remotely on Mondays and Fridays.

Salary Pay Range:

$192,050.00 - $263,350.00 USD Salary

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or trainingIn addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensationYour recruiter can share more about the specific salary range for your preferred location during the hiring process.

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences

About Integra LifeSciences

Integra LifeSciences is an American company that develops, manufactures, and markets medical devices for use in neurosurgery, extremity reconstruction, orthopedics, and general surgery. The company's products include implants, devices, instruments, and systems used in neurosurgery, neuromonitoring, neurotrauma, and related critical care. Integra LifeSciences has its headquarters in Princeton, New Jersey.
Learn more about Integra LifeSciences
Size
3,800 employees
Market Cap
$4.6 billion
Industry
Net Income
$133.8 million
Founded
1989
5 Year Trend
+9.2%
Revenue
$1.3 billion
NASDAQ

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