Quality Systems Leader

Philips

Cambridge (AL)

On-site

USD 102,000 - 143,000

Full time

6 days ago
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Job summary

Philips in Cambridge, MA is seeking a QMS Manager to lead the QMS team and oversee quality management activities in line with company policies. The role supervises day‑to‑day QMS operations, deploys and maintains document control, training, and internal audits, and analyzes metrics to drive improvement. Applicants should hold a Bachelor’s or Master’s in engineering or science, have 3+ years in quality/QMS roles, and ideally 5+ years with medical device regulations; onsite office position.

Qualifications

  • Must have a Bachelor’s or Master’s degree in engineering or science.
  • 3+ years of experience in quality/QMS roles.
  • 5+ years of experience with medical device regulations and standards; QMS management preferred.
  • Office/Remote work requirements and environment stated in the posting.

Responsibilities

  • Supervises day-to-day operations of the QMS team and ensures quality processes comply with company policies.
  • Manages deployment and maintenance of QMS processes (document control, training, internal audits)
  • Monitors and reports on QMS performance, identifies trends, and implements action plans for improvement.
  • Prepares for and supports external audits and inspections; manages NCRs and corrective actions.
  • Conducts risk assessments and develops mitigation strategies to protect product quality.

Skills

Quality management
Leadership
Data analysis
Risk management

Education

Bachelor’s / Master’s Degree in Engineering or Science

Job description

Philips in Cambridge, MA is seeking a QMS Manager to lead the QMS team and oversee quality management activities in line with company policies. The role supervises day‑to‑day QMS operations, deploys and maintains document control, training, and internal audits, and analyzes metrics to drive improvement. Applicants should hold a Bachelor’s or Master’s in engineering or science, have 3+ years in quality/QMS roles, and ideally 5+ years with medical device regulations; onsite office position.
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