Senior Quality Manager, Technology

Posted Yesterday
Be an Early Applicant
Hiring Remotely in United States
Remote
128K-188K Annually
Senior level
Healthtech • Manufacturing
The Role
Lead the strategy, governance, validation, adoption, and sustainment of quality technologies in an FDA-regulated medical device environment. Oversee QMS, MES, LMS, software assurance, data integrity, electronic records, CSA, audit readiness, and digital quality transformation. Build business cases, define roadmaps and requirements, guide regulatory risk management, and partner across Quality, IT, Operations, Engineering, Regulatory, and site leadership. Lead and develop a global team while driving compliant, user-focused technology adoption and continuous improvement.
Summary Generated by Built In

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.

At Integer, our values are embedded in everything we do.

Customer

We focus on our customers’ success

Innovation

We create better solutions

Collaboration

We create success together

Inclusion

We always interact with others respectfully

Candor

We are open and honest with one another

Integrity

We do the right things and do things right

Accountabilities & Responsibilities:

Strategy, Roadmap & Value Acceleration

  • Partner with Global Quality Systems leadership to define QMS technology strategy, annual priorities, roadmaps, and measurable objectives.
  • Align stakeholders on standard, scalable technology solutions that support business strategy, customer expectations, and global quality priorities.
  • Quantify the value of quality technology programs, including improvements in quality, compliance, productivity, cost, speed, and user experience.
  • Translate emerging quality technology needs into business cases, user and functional requirements, governance expectations, and execution plans.

Regulated Technology Leadership & Technical Oversight

  • Provide quality technology leadership and design-authority input for acquisition integration, new site adoption, digital transformation and enterprise programs that impact regulated quality processes.
  • Ensure requirements, intended use, regulatory risk, validation strategy, data integrity, electronic records, change control, and sustainment needs are defined and maintained through the system lifecycle.
  • Provide technical leadership across regulatory requirements, risk management, validation, CSA, data integrity, electronic records, automated inspection, and AI/ML.
  • Support audit readiness for enterprise quality systems and regulated technologies, including validation, training records, electronic records, data integrity, and QMS governance.

Innovation & Digital Quality Enablement

  •        Partner with IT and business leaders to evaluate, implement, and scale digital quality solutions that improve speed, control, visibility, compliance, user adoption, and enterprise value.
  •        Drive adoption of data-driven, AI-enabled, and risk-based CSA approaches that modernize regulated quality technology practices.
  • Represent Integer in external industry advisory groups and meetings, where appropriate, to help shape and learn from evolving best practices in regulated quality technology

Training, Adoption & Enterprise Enablement

  • Partner with Global Process Owners, subject matter experts, IT, and Training to define practical training, coaching, and adoption approaches for enterprise quality technologies.
  • Ensure deployments include role-based training, user guidance, adoption support, and sustainment expectations.
  • Promote solutions that are simple, scalable, user-focused, and designed to reduce friction for frontline associates and business users.

Team Leadership & Talent Development

  • Lead, coach, and develop a team responsible for digital quality enablement, GxP training governance, software assurance, and enterprise platform support.
  • Establish clear priorities, objectives, communication routines, and decision pathways that align team efforts to business priorities, program milestones, site needs, and individual development plans.
  • Remove barriers, escalate risks, and coordinate cross-functional support when issues require decisions across Quality, IT, Operations, Engineering, Regulatory, or site leadership.
  • Build a culture of accountability, teamwork, inclusion, continuous improvement, and mutual trust.

Governance, Compliance & Quality Culture

  • Ensure quality technology solutions are effective and comply with company policies, QMS requirements, environmental requirements, FDA regulations, global standards, and applicable regulatory expectations while supporting ongoing audit readiness.
  • Champion accountability, innovation, continuous improvement, and the mindset of “I own Quality.”

Education & Experience:

Minimum Education:

  • Bachelor’s degree in Engineering, Life Sciences, Information Systems, or a related technical field required.

Minimum Experience:

  • 8+ years of experience in Quality, IT, Operations, or related functions within an FDA regulated environment.
  • 3+ years of supervisory or leadership experience.
  • You have experience implementing, validating, governing, or sustaining technologies used in FDA-regulated environments, including QMS, MES, LMS, and related enterprise platforms.
  • You can demonstrate ability to drive adoption of new technology by balancing compliance, user experience, business value, and operational practicality.

Knowledge & Skills You Need:

  • Strong working knowledge of regulated quality technology, including CSV/CSA, electronic records, data integrity, and lifecycle governance.
  • Working knowledge of medical device quality system requirements, including EU MDR, ISO 13485, ISO 9001, GMP, 21 CFR 820, Good Documentation Practices, FDA CSA Guidance, and audit expectations.
  • A continuous improvement mindset and strong drive to overcome challenges in achieving goals and delivering results.
  • Ability to translate complex regulatory, technical, and business needs into practical requirements, governance models, and implementation plans.
  • Strong cross-functional leadership, concise communication and influence skills across Quality, IT, Operations, Engineering, Regulatory, and site leadership.
  • Ability to build, lead, and develop global teams while communicating clearly with executive, technical, regulatory, and frontline audiences.

Salary Range: $128,250.00 - $188,100.00

Our total rewards program is designed to attract, retain, and motivate associates to contribute to Integer’s success. Our compensation program includes base salary and a cash-based incentive program supporting our pay-for-performance philosophy. We provide a comprehensive benefits package with immediate eligibility including medical, dental, vision, disability, life insurance, and adoption benefits. Parental leave is available after one year. Optional employee-paid programs include supplemental life insurance, critical illness, hospital indemnity and accident insurance. Employees are immediately eligible to participate in the 401(k) plan with company matching contributions. We provide 80 hours (10 days) of company designated holidays per year plus an annual allotment of paid time off.

U.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.

Skills Required

  • Bachelor's degree in Engineering, Life Sciences, Information Systems, or a related technical field
  • 8+ years of experience in Quality, IT, Operations, or related functions within an FDA-regulated environment
  • 3+ years of supervisory or leadership experience
  • Experience implementing, validating, governing, or sustaining technologies used in FDA-regulated environments, including QMS, MES, LMS, and related enterprise platforms
  • Ability to drive adoption of new technology while balancing compliance, user experience, business value, and operational practicality
  • Working knowledge of regulated quality technology, including CSV/CSA, electronic records, data integrity, and lifecycle governance
  • Working knowledge of medical device quality system requirements, including EU MDR, ISO 13485, ISO 9001, GMP, 21 CFR 820, Good Documentation Practices, FDA CSA Guidance, and audit expectations
  • Ability to translate complex regulatory, technical, and business needs into practical requirements, governance models, and implementation plans
  • Strong cross-functional leadership, communication, and influence skills across Quality, IT, Operations, Engineering, Regulatory, and site leadership
  • Ability to build, lead, and develop global teams while communicating with executive, technical, regulatory, and frontline audiences

Integer Holdings Corporation Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Integer Holdings Corporation and has not been reviewed or approved by Integer Holdings Corporation.

  • Leave & Time Off Breadth PTO and paid holidays are often characterized as generous. Paid volunteer time further broadens time‑off options beyond core leave.
  • Retirement Support A 401(k) with company match and immediate vesting is highlighted. This structure provides accessible retirement savings support from the start.
  • Parental & Family Support Parental leave, adoption assistance, and family medical leave are included. Feedback suggests these offerings add meaningful non‑salary value for many roles.

Integer Holdings Corporation Insights

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The Company
HQ: Plano, TX
2,909 Employees
Year Founded: 1940

What We Do

Integer Holdings Corporation (NYSE:ITGR) is a leader in advanced medical device outsourcing (MDO) and serves its customers by providing comprehensive end-to-end solutions with its unparalleled expertise in innovation and manufacturing. Integer's vision is to enhance the lives of patients worldwide by being its customer's partner of choice for innovative medical technologies and services. Additionally, through Electrochem, an Integer company, it develops custom batteries for high-end niche applications in energy, military, and environment markets. The company's medical device manufacturing brands include Greatbatch™ Medical and Lake Region Medical™. Additional information is available at www.integer.net.

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