Quality Manufacturing Engineer

philips; United States; On-site; USD 92,000 - 128,000; Full time

Benefits offered by this job

PTO

401k match

HSA with company contribution

Stock purchase plan

Education reimbursement

Job summary

Philips is seeking a Quality Manufacturing Engineer to drive high-quality performance in its manufacturing sites in the United States. This role focuses on facilitating quality systems, CAPA, and process validation to support NPI and product transfers.

Ideal candidates hold a Bachelor’s or Master’s degree in Engineering or Science and have 3+ years in Quality/Process Engineering, with preference for medical device regulatory experience and data-driven problem-solving.

Qualifications

• Bachelor's or Master's degree in Mechanical/Electronics Engineering, Science or equivalent.
• 3+ years of experience in Quality/Process Engineering or equivalent.
• Experience with medical device regulations, CAPA, RCA, and data analysis preferred.

Responsibilities

• Facilitate operations performance monitoring, reporting, and development in manufacturing.
• Assess PFMEA impact and controls for design changes and transfers.
• Lead analysis of defects, manage non-conformances and CAPA actions.
• Ensure quality systems in manufacturing are maintained and support NPI/product transfers.
• Lead validation protocols and data analysis for process improvements and validation activities.

Skills

Quality Engineering

Process Engineering

CAPA

Root Cause Analysis

Data Analysis

Education

Bachelor's or Master's in Engineering/Science

Job description

Job Title

Quality Manufacturing Engineer

Job Description

In this role you

Are responsible for providing facilitation in achieving a state of high-quality performance and compliance in the factories and aid in providing oversight of Philips processes utilized in manufacturing,

Your role:

• Facilitates operations performance monitoring, reporting, improvement and development, facilitates improvement programs in factory, and supports analytical testing and Supplier Quality Engineering (SQE), Supplier Quality Assurance (SQA) and Purchasing.
• Conducts assessment of impact to Process Failure Mode and Effects Analysis (PFMEA) and associated controls in relation to design changes and assists in Manufacturing Process Development and Design Transfer activities.
• Leads analysis of defects for determining dispositions of non-conformances, drives management of Non-Conformances (NC) and Quality Notifications (QN) and facilitates implementation of effective Corrective and Preventive Actions (CAPA) actions.
• Facilitates timely quality engineering and quality assurance tasks, ensures manufacturing quality systems are maintained, handles single or complex process validation and process improvement activities, and helps in completion of New Product Introduction (NPI) and product transfers in factory.
• Leads validation protocols, facilitates production builds to support validation activities, analyzes data for reports, process improvement initiatives, and validation activities.

You're the right fit if:

• Bachelor's / Master's Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent.
• 3+ years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering or equivalent
• We prefer experience with medical device regulations and standards, Process Quality Management, CAPA, Root Cause Analysis, Data Analysis.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Office/Remote position.

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 5 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.

This is an office role.

About Philips

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. Do the work of your life to help improve the lives of others.

Learn more about our business .

Discover our rich and exciting history.

Learn more about our purpose.

Learn more about our culture.

Philips Transparency Details

The pay range for this position in Murrysville PA is $92,000 to $128,000 Annually.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. 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 .

At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Murrysville PA.

Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.