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Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 1 min ago
G
Civil Construction Estimator
GPAC
Cleveland, OH
- $100,000 to $120,000 USD / year
Analyze historical project costs and production data to improve estimating accuracy.
Added 4 mins ago
A
Manufacturing Technician I, MD Fill - B2 Shift
AbbVie
Waco, TX
- $18.6 to $24.5 USD / hour
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as…
Added 7 mins ago
A
Hiring Production Associate - Immediate Start!!
Aerotek
Buffalo Grove, IL
- $18 USD / hour
Manufacturing or production experience preferred Mechanical aptitude and ability to use hand and power tools Ability to stand for an 8-hour shift Comfortable using a computer and following…
Added 9 mins ago
G
Corporate Food Safety & Quality Manager
GPAC
Erin, NY
- $90,000 to $95,000 USD / year
Collect, analyze, and report Food Safety & Quality data from production and process improvement activities
Added 9 mins ago
G
Corporate Food Safety & Quality Manager
GPAC
Dryden, NY
- $90,000 to $95,000 USD / year
Collect, analyze, and report Food Safety & Quality data from production and process improvement activities
Added 9 mins ago
G
Corporate Food Safety & Quality Manager
GPAC
Lockwood, NY
- $90,000 to $95,000 USD / year
Collect, analyze, and report Food Safety & Quality data from production and process improvement activities
Added 9 mins ago
G
Corporate Food Safety & Quality Manager
GPAC
Newfield, NY
- $90,000 to $95,000 USD / year
Collect, analyze, and report Food Safety & Quality data from production and process improvement activities
Added 9 mins ago
G
Corporate Food Safety & Quality Manager
GPAC
Montour Falls, NY
- $90,000 to $95,000 USD / year
Collect, analyze, and report Food Safety & Quality data from production and process improvement activities
Added 9 mins ago
G
Corporate Food Safety & Quality Manager
GPAC
Watkins Glen, NY
- $90,000 to $95,000 USD / year
Collect, analyze, and report Food Safety & Quality data from production and process improvement activities
Added 10 mins ago
G
Warehouse Manager
GPAC
Sidney, OH
- $70,000 to $80,000 USD / year
Oversee receiving, storage, inventory control, and outbound shipping
Added 11 mins ago
Mine Geologist
JDS Energy & Mining
Challis · Challis, ID
Sampling & Assay Quality Control: Supervise production sampling programs (e.g., blast holes, sludge, or muck samples) and oversee QA/QC protocols before dispatching samples to the…
Added 11 mins ago
Pipeline Coordinator
JDS Energy & Mining
Challis · Challis, ID
…advancing pit or underground mine development without disrupting…
Added 12 mins ago
GIS Analyst - Fort Devens, MA
Colorado State University
CEMML - Devens, MA
…The position creates, updates, manages, and performs quality control on GIS data to ensure compliance with Army data standards. Responsibilities include geospatial analysis, map production,…
Added 12 mins ago
CG
SOUS CHEF (FULL TIME)
Compass Group, North America
Norwell, MA
- $23 to $25 USD / hour
- Full-time
Cooks and prepares food following approved recipes and production standards. Ensures all deadlines are met based on production orders.
Added 12 mins ago
Manufacturing Engineer 2 - Unmanned Underwater Vehicles (UUV) 31057
Huntington Ingalls Industries
Pocasset, MA
…contracting environment. This role focuses on hands-on support of production, integration, and testing activities while gaining experience with complex electromechanical systems,…
Added 12 mins ago
INGENYX- Process Engineer 3 - Quality
Teleflex
Mansfield, MA
Ingenyx is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades of experience, a…

Philips

Senior Quality Operations Engineer

Bedford, MA, United States

On-site

The pay range for this position in Bedford, MA is $102,480 to $163,968.

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Job details

Pay: The pay range for this position in Bedford, MA is $102,480 to $163,968.
Workplace: On-site
Posting language: English
Posted: Nov 7, 2026

Original job description

The Senior Quality Operations Engineer is responsible for supporting a state of high-quality performance, compliance, and oversight/performance monitoring of Philips manufacturing processes, driving compliance and continuous improvement throughout the manufacturing process.

Your role:

Support operations performance monitoring, reporting, improvement and development, facilitate quality improvement programs in factories.
Handles nonconformance events/investigations in the factory, leverages Process Failure Mode and Effects Analysis (PFMEA) to assess risk, guides material review board activities for non-conformance disposition management, leads analysis of defects for determining dispositions of non-conformances, drives management of Non-Conformances (NC) 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.
Possesses working knowledge Quality Engineering and Continuous Improvement techniques, follows processes and operational policies in selecting methods for obtaining solutions, and frequently interacts with supervisors and functional peer groups to gain cooperation of others
Leads validation protocols, facilitates production builds to support validation activities, analyzes data for reports, process improvement initiatives, and validation activities.
Utilizes advanced statistical analysis methods to interpret complex data trends, resolve a wide range of moderate complexity requests, and provide strategic insights for continuous enhancement of quality standards and process efficiency.
Ability to interpret and/or create detailed, quality metrics and reports with stakeholders, highlighting significant achievements, emerging trends, and actionable insights to drive advanced improvement initiatives and ensure regulatory compliance.
Delivers training programs on quality standards, advanced methodologies, and best practices, fostering alignment across functions and advancing excellence in operational practices at an high proficiency level.
Experience managing incoming inspection programs, equipment control processes (including calibration and maintenance), environmental monitoring programs (viable and non-viable) including data analysis and trending, and support sterilization, endotoxin process analysis to ensure compliance with regulatory and quality requirements.

You're the right fit if:

You have a minimum of 5+ years’ experience in FDA regulated (ISO 13485) medical device quality operations/manufacturing environments, with a focus on quality operations, audit support, process validation/improvement, CAPA, non-conformance, PFMEA’s and Change/Risk Management (ISO 14971).
You have proven experience leading cross-functional teams
You have detailed experience/knowledge in CAPA processes non-conformances, including problem identification, root cause analysis, implementation of solutions to prevent recurrence and drive continuous improvement.
You’re experienced in utilizing Quality) insights/data analytics to lead continuous improvement.
You’re able to build/cultivate relationships with supervisors, functional peer groups, internal/external stakeholders, suppliers etc.
Previous experience in environmental control programs and sterilization validation.
You have a minimum of a Bachelor’s Degree in Engineering. ASQ-CQE, ISO Lead Auditor certifications-desired
You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.

How we work together:

We believe that we are better together than a part. For our Office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time (5 days per week) 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 ON-SITE 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 Bedford, MA is $102,480 to $163,968.

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.

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.

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.

Additional Information:

US work authorization is a precondition of employment. T he 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 Bedford, MA.
May require travel up to 10%.

It is the policy of Philips to provide equal employment and advancement opportunities to all colleagues and applicants for employment without regard to race, color, ethnicity, religion, gender, pregnancy/childbirth, age, national origin, sexual orientation, gender identity or expression, disability or perceived disability, genetic information, citizenship, veteran or military status or a person’s relationship or association with a protected veteran, including spouses and other family members, marital or domestic partner status, or any other category protected by federal, state and/or local laws.

As an equal opportunity employer, Philips is committed to a diverse workforce. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance.

Equal Employment and Opportunity Employer/Disabled/Veteran

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More about this job

Skills

Regulatory compliance
Manufacturing processes
Process improvement
Reporting
Quality assurance
Quality control systems
Statistics
Inspection
Data analysis
Risk management
Root cause analysis

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