Operations Quality Manager

Philips • Fremont, CA

10h • Onsite

About The Position

The Operations Quality Manager will manage the Quality Operations team and coordinates, designs and executes activities for multiple Quality Operations projects, effectively ensuring alignment with corporate goals and compliance with all regulatory requirements for Philips’ Image Guided Therapy Devices (IGTD). Your role: Responsible for implementing policy changes, ensuring product quality, managing manufacturing processes, coordinating product inspections, qualifying materials, overseeing supplier processes, executing recall procedures, producing quality assurance deliverables, and fostering collaboration across departments to achieve project goals and operational excellence. Manages/mentors the Quality Operations team, contributing to employee selection, performance management, career development, and overseeing operational processes. Implement quality processes and tools necessary to ensure product quality and enhance customer satisfaction, fostering a culture of excellence and continuous improvement within the organization. Manages the review and approval of finished products manufactured, coordinates all inspections and inquiries regarding the operation of manufacturing site to ensure compliance with company standards and manufacturing process specifications. Participates in cross-functional teams as a Quality technical resource responsible for providing quality oversight and support to manufacturing operations within Philips or at contracted suppliers. Drives quality investigations and reviews corrective action plans for adequacy and compliance. This includes root cause analysis and product impact assessments for investigations resulting from nonconformances. Supports internal /external audit programs, assists in preparation of audit responses and leads CAPA activity-CAPA board, reviews investigations, ensures appropriate CAPA actions, may own CAPA. Manages- calibration activities for instrumentation, measurement and test equipment, resource optimization, and incoming material and outgoing product acceptance activities, resource optimization, and compliance with regulations. Monitors operational key performance indicators (KPIs), Identifies, facilitates, and/or leads continuous improvement efforts and maintains Quality Metrics to support process improvement activities. Responsible for coordinating, facilitating and follow up on any Quality Leadership Team action items assigned.

Requirements

• You have a minimum of 5+ years’ experience in FDA regulated medical device environments, with a focus on Operations Quality (IQ/OQ/PQ), process/continuous improvement, CAPA activities and internal /external audit programs.
• You have experience leading quality teams/projects, functional team management experience (desired), including budgeting, workforce planning, Performance Management, Employee Engagement/ Retention, Succession Planning, coaching, training, etc.
• You have strong understanding of Medical Device regulations/standards including ISO 13485/14971, 21CFR (803, 806, 820, etc.), MDD/ EU MDR, cGMP, and GDP.
• You have proven experience utilizing Quality KPI’s/Data Analysis to assess project performance and identify process and continuous improvement opportunities.
• You’re able to effectively communicate, influence and build relationships with cross-functional team members, internal/external stakeholders at all levels, suppliers, and able to manage/facilitate audits and inspections with the FDA, competent authorities, Regulatory Agencies and Notified Body.
• You have a minimum of a Bachelor’s degree in Quality, Engineering or a related Scientific discipline (required).
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position .

Nice To Haves

• ASQ certifications (desired).

Responsibilities

• Implementing policy changes
• Ensuring product quality
• Managing manufacturing processes
• Coordinating product inspections
• Qualifying materials
• Overseeing supplier processes
• Executing recall procedures
• Producing quality assurance deliverables
• Fostering collaboration across departments
• Managing/mentoring the Quality Operations team
• Implementing quality processes and tools
• Managing the review and approval of finished products manufactured
• Participating in cross-functional teams as a Quality technical resource
• Driving quality investigations and reviews corrective action plans
• Supporting internal /external audit programs
• Managing calibration activities for instrumentation, measurement and test equipment
• Monitoring operational key performance indicators (KPIs)
• Identifying, facilitating, and/or leads continuous improvement efforts
• Maintaining Quality Metrics to support process improvement activities
• Responsible for coordinating, facilitating and follow up on any Quality Leadership Team action items assigned

Benefits

• Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.
• Details about our benefits can be found here .

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Number of Employees: 5,001-10,000 employees