Senior Operations Quality Manager

Philips UK

Plymouth, United States
$120,488 to $192,780; not specified; generous pto,...
Fully remote
Fda regulated medical device environments
Operations quality (iq/oq/pq)
Process/continuous improvement
The Senior Operations Quality Manager will manage the Quality Operations team and be the Site leader for our Plymouth, MN Image Guided Therapy Devices (IGTD) site, ensuring alignment with corporate goals and compliance with all regulatory requirements

Job Summary

  • The Senior Operations Quality Manager will manage the Quality Operations team and be the Site leader for our Plymouth, MN Image Guided Therapy Devices (IGTD) site, ensuring alignment with corporate goals and compliance with all regulatory requirements.
  • Responsible for functional team management including operations, budgeting, workforce planning, Performance Management, Employee Engagement/ Retention, Succession Planning, communicating job expectations, planning, coaching, training, and developing personal growth opportunities.
  • We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve.

Matching Summary

The Senior Operations Quality Manager will manage the Quality Operations team and be the Site leader for our Plymouth, MN Image Guided Therapy Devices (IGTD) site, ensuring alignment with corporate goals and compliance with all regulatory requirements.

Salary

$120,488 to $192,780; Not specified; Generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement

Skills & Requirements

Must-have

  • FDA regulated medical device environments
  • Operations Quality (IQ/OQ/PQ)
  • process/continuous improvement
  • CAPA activities
  • internal /external audit programs
  • ISO 13485/14971, 21CFR, MDD/ EU MDR, cGMP, GDP

Nice-to-have

  • drug-device combination products preferred
  • ASQ certifications
  • cultivate and maintain strong relationships

Key Requirements

  • Minimum 10+ years experience in FDA regulated medical device environments
  • Minimum 3+ years experience in functional team management
  • Bachelor’s degree in Quality, Engineering or related Scientific discipline
  • US work authorization required

Work Rights

Must have US work authorization

Tailored Resume

Cover Letter