Siemens Healthineers

DX Head of Regions Quality Management and Regulatory Affairs

Siemens Healthineers$240K — $330K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • 15+ years in Quality and/or Regulatory Affairs within medical device/pharma, including leadership responsibility.
  • Strong experience with QMS, regulatory submissions/approvals, and inspections (e.g., FDA/NMPA).
  • Proven success leading Quality & Regulatory organizations in complex, international settings.
  • Experience in global process harmonization and standardization across various countries.
  • Degree in Life Sciences, Engineering, or a related discipline.

Responsibilities

  • Lead and develop regional Quality & Regulatory leadership teams across multiple regions.
  • Establish a harmonized global operating model for Quality & Regulatory processes.
  • Drive consistency in Quality Management Systems and promote continuous improvement.
  • Foster cross-regional collaboration to enhance efficiency and compliance.
  • Maintain and improve the Quality Management System to satisfy business requirements.
  • Identify and mitigate quality risks through structured management.
  • Define and execute the regional regulatory strategy for timely submissions.

Benefits

  • Medical, dental, and vision insurance.
  • 401(k) retirement plan.
  • Life insurance and disability insurance.
  • Paid parking/public transportation.
  • Paid time off and paid sick/safe time.
Full Job Description

Position: DX Head of Regions Quality Management and Regulatory Affairs Head
Location: US East coast

Mission / Position summary:

  • Lead the Regional Quality & Regulatory Affairs organization across North America, EMEA, APAC, and Latin America, driving a harmonized, standardized, and high-performing operating model that ensures regulatory compliance, product safety, and operational excellence across Commercial Operations and Customer Services.
  • Serve as the Regional Head of Quality & Regulatory Affairs for North America, ensuring compliance, product quality, and business continuity across commercial operations and customer services.
  • Develop and execute regional Quality & Regulatory strategies, translating regulatory requirements into pragmatic business actions that enable market access, customer satisfaction, and sustainable growth.
  • Act as the Quality Representative for assigned legal entities, fostering a risk-based quality culture that balances regulatory compliance with business objectives.

Key responsibilities:


Global Regions leadership

  • Lead and develop the Regional Quality & Regulatory leadership teams across EMEA, APAC, and Latin America, driving capability, accountability, and performance.
  • Establish a harmonized global operating model by standardizing Quality & Regulatory processes, governance, tools, and best practices across all regions.
  • Drive consistency in Quality Management Systems, regulatory execution, performance metrics, and continuous improvement while enabling appropriate regional flexibility.
  • Foster cross-regional collaboration, knowledge sharing, and operational excellence to improve efficiency, compliance, and customer outcomes.



Quality Management & Continuous Improvement NAM

  • Maintain and continuously improve the Quality Management System (QMS) to meet regulatory and business requirements.
  • Ensure effective execution of Quality Assurance and Quality Engineering processes (e.g., audits, training, documentation, CAPA, nonconformance management).
  • Identify and mitigate quality risks in commercial operations through structured risk management.
  • Drive process improvements that increase efficiency, product quality, and customer satisfaction.
  • Leverage digital tools and data insights to enhance quality performance, transparency, and decision-making.



Regulatory Strategy & Compliance NAM

  • Define and execute the regional regulatory strategy, ensuring timely submissions, approvals, and adherence to country-specific requirements.
  • Ensure full compliance with internal policies and external regulations, with a strong focus on product safety and market access. Translate regulatory requirements into clear business implications and actionable guidance for leadership teams
  • Act as key interface to health authorities and external stakeholders, representing the organization with credibility and impact.

Commercial & Customer Quality NAM

  • Ensure product integrity and compliance across commercial operations and customer services.
  • Ensure on time and accurate Post Market Surveillance & Reporting
  • Partner with customer-facing teams to resolve quality issues and improve the end-to-end customer experience.

Leadership & Stakeholder Management

  • Embed a strong quality culture focused on continuous improvement and customer-centricity.
  • Build and lead a high-performing regional Quality & Regulatory team, driving accountability, capability, and ownership.
  • Collaborate closely with global Quality and cross-functional teams to align standards, share best practices, and ensure consistent execution.

Your qualifications and experience:

  • 15+ years in Quality and/or Regulatory Affairs within medical device / pharma, including leadership responsibility.
  • Strong experience with QMS, regulatory submissions/approvals, inspections (e.g., FDA/NMPA), and product safety/compliance frameworks.
  • Proven success leading Quality & Regulatory organizations in complex, international matrix environments.
  • Experience driving global process harmonization, standardization, and implementation of Quality Management Systems across multiple countries and cultures.
  • Degree in Life Sciences, Engineering, or a related discipline.

Competency Requirements:

  • Deep expertise in Quality & Regulatory frameworks, including QMS, audits, and authority interactions.
  • Ability to translate regulatory requirements into clear business actions and decisions.
  • Strong analytical, data-driven, and problem-solving mindset.
  • Effective stakeholder management and communication in global, cross-functional settings.
  • Proven ability to lead, develop, and drive performance of high-performing teams.
  • High ownership, execution focus, and change agility.
  • Fluent in English.

#LI-ES1

#LI-REMOTE


The base pay range for this position is:

$240,000 - $330,000

Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.

If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.

About Siemens Healthineers

Siemens Healthineers is a medical technology company that provides a range of medical devices and services. The company was founded in 2018 and is headquartered in Erlangen, Germany. Siemens Healthineers operates in over 70 countries and has over 54,000 employees. The company is a subsidiary of Siemens AG, a German multinational conglomerate. Siemens Healthineers has been recognized for its innovation and commitment to sustainability.
Learn more about Siemens Healthineers
Size
54,000 employees
Industry
Founded
2008

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