Quality Systems Documentation Control Specialist

The Davis Companies

Burlington (MA)

On-site

USD 70,000 - 95,000

Full time

7 days ago
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Benefits offered by this job

On-site role
Bonus potential 15%
Direct hire

Job summary

The Davis Companies in Massachusetts, Burlington, is seeking a motivated Document Control & Quality Systems Coordinator to join our manufacturing quality team. You will manage controlled documents, coordinate corrective actions, support internal and external audits, and ensure ISO 9001 (ISO 13485 preferred) compliance.

This on-site role offers a clear path for growth in a fast‑paced industrial environment with strong emphasis on precision and traceability.

Qualifications

  • 3+ years in Quality Systems, Document Control, or Quality Assurance.
  • Experience with supplier/internal corrective actions.
  • Hands-on involvement in internal audits.
  • Working knowledge of calibration programs.
  • Strong understanding of ISO 9001 (ISO 13485 preferred).
  • Manufacturing experience.
  • Exceptional organizational and documentation skills.

Responsibilities

  • Quality Systems — Maintain controlled documents (SOPs, work instructions, specs, forms) and manage revisions, change requests, and approvals.
  • Document Control — Ensure airtight retention, archival, and training record accuracy.
  • Corrective Actions — Track supplier/internal CARs & SCARs, drive closure, and support root‑cause investigations.
  • Audit Support — Participate in internal audits and help prepare for external and customer audits.
  • ISO Compliance — Support ongoing compliance with ISO 9001; ISO 13485 experience is a strong plus.
  • Calibration Programs — Coordinate calibration schedules and maintain audit‑ready equipment records.
  • SAP Quality Processes — Manage quality records, workflows, and reporting through SAP.
  • Continuous Improvement — Contribute to quality KPIs and process optimization initiatives.

Skills

Quality Systems
Document Control
Quality Assurance
Corrective Actions
Internal Audits
Calibration Programs
ISO 9001
ISO 13485
Manufacturing Experience
Documentation Skills

Tools

SAP

Job description

Now Hiring: Document Control & Quality Systems Coordinator

Passionate about industrial automation, precision, and building world‑class manufacturing systems? This role puts you at the center of quality excellence. Growing company with a path for success which rewards its employees with both individual and company based bonuses, hiring immediately on a direct hire basis for top talent in quality documentation control. This is an on-site role with a potential for 15% bonus.

What You’ll Own

  • Quality Systems — Maintain controlled documents (SOPs, work instructions, specs, forms) and manage revisions, change requests, and approvals.
  • Document Control — Ensure airtight retention, archival, and training record accuracy.
  • Corrective Actions — Track supplier/internal CARs & SCARs, drive closure, and support root‑cause investigations.
  • Audit Support — Participate in internal audits and help prepare for external and customer audits.
  • ISO Compliance — Support ongoing compliance with ISO 9001; ISO 13485 experience is a strong plus.
  • Calibration Programs — Coordinate calibration schedules and maintain audit‑ready equipment records.
  • SAP Quality Processes — Manage quality records, workflows, and reporting through SAP.
  • Continuous Improvement — Contribute to quality KPIs and process optimization initiatives.

What You Bring

  • 3+ years in Quality Systems, Document Control, or Quality Assurance
  • Experience with supplier/internal corrective actions
  • Hands‑on involvement in internal audits
  • Working knowledge of calibration programs
  • Strong understanding of ISO 9001 (ISO 13485 preferred)
  • Manufacturing experience
  • Exceptional organizational and documentation skills

Why This Role Matters

Industrial automation thrives on precision, repeatability, and compliance. This position ensures the systems behind the machines are just as reliable as the machines themselves. If you love structured processes, quality excellence, and supporting high‑tech manufacturing environments, this role is built for you.

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