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Design Control Process Manager

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Remote

Design Control Process Manager

Ladders

Design Control Process Manager

Skills

Testing & QARCompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

United States

Work mode:

Remote

Published on:

25 August 2026

What they need


For our client, we are seeking a Design Control Process Manager to join the team of a leader in the Healthcare space. This role will lead operational priorities where safety, quality, compliance, and execution discipline are central to success. You will collaborate with field leadership, support functions, and cross-functional stakeholders to improve accountability, service delivery, and operational consistency. The position offers the opportunity to influence operational scale, customer outcomes, and organizational performance within a healthcare environment.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $151,000 – $196,000 annually

Responsibilities

  • Develop and improve design control processes governing medical device development
  • Ensure integration of design control processes with FDA and ISO compliance
  • Translate regulatory requirements into practical procedures and tools
  • Evaluate design control effectiveness and recommend updates based on quality data
  • Create implementation plans for new design control requirements across projects
  • Establish processes for accurate and audit-ready Design History Files
  • Manage quality assurance methods for product design and development

Qualifications

  • BS in Engineering or related technical discipline
  • 12+ years of experience in medical device Quality Assurance or Design Assurance
  • Expertise with FDA 21 CFR 820, 21 CFR Part 11, ISO 13485, and ISO 14971
  • Familiarity with IEC 60601, IEC 62366, and IEC 62304 standards
  • Proficiency in QMS software (e.g., MasterControl, Veeva Vault) and Document Control systems
  • Strong cross-functional influence and adherence capabilities
  • Proven ability to collaborate with Quality, Regulatory, R&D, and Manufacturing teams

Benefits

  • Remote work opportunities
  • Collaborative work environment with cross-functional teams
  • Opportunities for professional growth and development
  • Involvement in impactful medical device innovation
  • Supportive culture for quality and regulatory excellence

Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.

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