Job Title

Job Description

Job Responsibilities

• Owns and drives the quality performance of manufacturing processes, ensuring processes consistently meet defined quality, regulatory, and product requirements.
• Monitors process quality performance using KPIs such as First Time Right (FTR), DPU/DPMO, yield, defects, rework, scrap, and process capability.
• Identifies process quality risks and leads initiatives to reduce process variation, defects, and quality escapes.
• Performs structured root-cause analysis of manufacturing defects and process failures using 5-Why, Fishbone, 8D, DMAIC, and other problem-solving methodologies.
• Leads and facilitates investigation of Non-Conformances (NCs), Quality Notifications (QNs), and manufacturing-related quality issues.
• Defines and implements effective containment, corrective, and preventive actions to eliminate process-related defects and prevent recurrence.
• Provides quality input to PFMEA, Control Plans, process flows, work instructions, and manufacturing documentation.
• Supports and leads process validation and re-validation activities, including protocol development, execution, data analysis, and validation reports.
• Supports NPI, design transfer, and production ramp-up, ensuring appropriate quality controls are established before production release.
• Works closely with Manufacturing, Process Engineering, R&D, PQE, SQE, Supplier Quality, and Operations to resolve complex process-quality issues.
• Establishes and monitors process quality control plans and ensures effective implementation on the production floor.
• Performs regular analysis of quality trends and identifies emerging process risks before they result in significant quality events or customer impact.
• Participates in internal and external audits and provides technical support related to manufacturing process controls and quality.

Minimum Required Education

• Bachelor's degree in Industrial Engineering, Quality Engineering, or equivalent.

Minimum Required Experience

• 2+ years of experience in Quality Engineering, Process Engineering, or a related field.
• Experience working in a manufacturing environment.
• Experience with root-cause analysis, quality improvement, and manufacturing processes.

Preferred Experience

• Experience in medical devices or another regulated industry.
• Experience with PFMEA, Control Plans, and process validation.
• Experience with NC, QN, CAPA, and change management processes.

Compensation & benefits
Doing meaningful work should come with fair, transparent rewards. The base salary range for this role is 20000 Nis–25000 Nis. We determine pay within the range using objective factors, like the skills the role requires, your relevant experience and the responsibility you'll have in this role, alongside internal equity and local market considerations.
This role is eligible for bonus, with your rewards linked to [KPIs/company results]. We’ll share the full approach with you during the interview process, so you can make a clear, informed decision.

How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
About Philips
Are you ready to do the work of your life to help the lives of others? Learn more about our business, discover our rich and exciting history and learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care.

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