Quality Manager - ISO & CAPA Leader (Manufacturing)

Brook + Whittle

Guilford (CT)

On-site

USD 110,000 - 140,000

Full time

10 days ago
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Job summary

Brook + Whittle in Guilford, CT is seeking a Quality Manager to lead the quality department and own site quality performance. You will drive initiatives supporting key objectives, ensuring GMP/ISO/QMS compliance across facilities and steering future certification efforts.

Manufacturing experience is strongly preferred, with hands-on leadership, CAPA investigation expertise, and a proven track record in process improvement and cross-functional collaboration to monitor metrics and deliver

Qualifications

  • Bachelor’s degree with an emphasis in manufacturing, engineering, quality management.
  • 5+ years quality and/or process improvement experience preferred.
  • Experience with ISO 9001 or equivalent; other standards a plus.
  • Experience working with customers preferred.
  • Strong leadership and management skills.
  • Excellent interpersonal, oral, written communication skills.
  • Familiar with company/industry quality standards and processes.

Responsibilities

  • Drive quality throughout the business with hands-on support.
  • Own the future ISO Program at the Guilford site.
  • Ensure customer quality standards are documented and communicated to customers as required.
  • Manage QA staff to increase product quality.
  • Lead CAPA investigations and root-cause analysis for issues.
  • Collaborate on cross-location quality initiatives and projects.
  • Develop value streams and process maps to standardize workflows.
  • Deploy quality/delivery/cost metrics and management routines.

Skills

Leadership
Management
Quality standards
Communication
Influence
Business analysis
Process improvement
Project management

Education

Bachelor's degree in manufacturing/engineering/quality

Job description

Brook + Whittle in Guilford, CT is seeking a Quality Manager to lead the quality department and own site quality performance. You will drive initiatives supporting key objectives, ensuring GMP/ISO/QMS compliance across facilities and steering future certification efforts.

Manufacturing experience is strongly preferred, with hands-on leadership, CAPA investigation expertise, and a proven track record in process improvement and cross-functional collaboration to monitor metrics and deliver

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