Top 43767 Sr. engineer, process development wayne, nj Jobs in New Jersey

Sr. Engineer, Process Development - Wayne, NJ
Maquet Cardiovascular LLC —Wayne, NJ
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- Master's degree
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Centerview Health —Toms River, NJ
- $220,000 - $260,000 a year
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GARFIELD PARK ACADEMY —Willingboro, NJ
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Ocean Heart Group —Township of Brick, NJ
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Rothstein Mandell Strohm Halm & Cipriani —Toms River, NJ
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- 4 years
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Primary Care Physician - New Grads Preferred
Hathaway Healthcare —Whiting, NJ
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Beattie Padovano, LLC —Montvale, NJ
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- Email
- 5 years
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Nursing Clinical Coordinator
Eastern International College —Jersey City, NJ
- $90,000 - $95,000 a year
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Pain Management & Regenerative Medicine Physician (MD)
Madison Medical Sports & Rehabilitation Center —Madison, NJ
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Clinical Supervisor
Inner Clarity, LLC —Hazlet, NJ
- $80 - $100 an hour
- Part-time
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- LMFT
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- LPC
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Outside Sales Representative
Generac Power Systems —Morganville, NJ
- From $80,000 a year
- Full-time
- Mid-level
- Residential
- Driver's License
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Criminal Defense Attorney
Law Offices of Jonathan F. Marshall —Freehold, NJ
- $90,000 - $175,000 a year
- Full-time
- Hybrid work
- Mid-level
- Residential
- Health insurance
- Dental insurance
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Primary Care / Sports Medicine Physician (MD or DO)
Madison Medical Sports & Rehabilitation Center —Madison, NJ
- $200,000 - $230,000 a year
- Full-time
- Medicine
- Internal Medicine
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Orthopedic Surgeon
Oasis Medical and Surgical Wellness Group —Union, NJ
- $1 - $2 a year
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SLP / Speech Language Pathologist - Home Health
Adoration Health —Clifton, NJ
- $60 - $70 an hour
- Full-time
- CPR Certification
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Arbitration Relations Counsel (Attorney)
Forthright —Somerset, NJ
- $125,000 - $140,000 a year
- Full-time
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- 7 years
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Physician Assistant
Avenel Iselin Medical Group —Iselin, NJ
- $140,000 a year
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Physical Therapist - Outpatient Orthopedics
Riptide Physical Therapy —Barnegat, NJ
- Full-time
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- Doctoral degree
- Physical & Rehabilitation Medicine
- Continuing education credits
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Sr. Engineer, Process Development - Wayne, NJ

Maquet Cardiovascular LLC -
Wayne, NJ

Apply Now

Job Details

$115,000 - $135,000 a year

Benefits

Commuter assistance
Caregiver leave
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Vision insurance
401(k) matching
Life insurance

Qualifications

Six Sigma methodology implementation
GD&T
Production validation processes
Biomedical regulatory compliance
Biomedical manufacturing processes
Manufacturing company experience

Full Job Description

Date: Jul 14, 2026

Location:
Wayne, NJ, US

Company: Maquet Cardiovascular LLC
Remote Work: 1-2 days at home (site based)
Salary Range: $115,000 - $135,000 per year depending on experien

With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

Job Overview

This position provides technical leadership in development, optimization, validation, and design transfer of medical device manufacturing processes from R&D into commercial production
This role ensures that processes are robust, scalable, and compliant with regulatory and quality standards including FDA 21 CFR Part 820 and ISO 13485.
Leadership in process development, validation, statistical analysis, and cross-functional collaboration, with a proven ability to drive successful product introductions in a regulated environment.

Job Responsibilities and Essential Duties

Process Development

Technical and team leadership in the development, characterization and optimization of manufacturing processes for new and existing products.
Supports the definition and development of product requirements, specifications and working parameters using current engineering methods and technologies.
Lead large scale process validations strategies (IQ/OQ/PQ), process characterization efforts, and statistical justification aligned with regulatory expectations.
Apply DFSS tools (DOE, SPC, capability analysis) to improve process performance and robustness.

Design Transfer

Responsible for the design transfer activities from R&D to Manufacturing, ensuring readiness for commercial production.
Partner with a cross-functional team to ensure designs are manufacturable, scalable, and cost-effective (DFM/DFA).
Support product launches, including pilot builds and ramp-to-production activities
Ensure compliance with FDA, ISO 13485 and internal quality systems.
Conduct and support risk management activities (FMEA, hazard analysis).
Participate in audits and inspections, providing technical expertise and documentation support.

Cross-Functional Collaboration

Act as the primary technical interface in a cross-functional team as a Core Team member
Partner with Operations and Quality to enhance throughput, reduce scrap, and expand manufacturing capacity.
Provide guidance and mentorship to junior engineers and technicians.

Continuous Improvement

Identify and drive process improvement initiatives using Lean and Six Sigma methodologies.
Monitor and analyze process performance metrics to improve yield, reduce scrap, and increase efficiency.
Support CAPA investigation and implement sustainable solutions.

Minimum Requirements

Master’s (Preferred) or bachelor’s degree in Mechanical, Biomedical Engineering or related technical field with 5 – 7 years of experience.
Demonstrated experience in Process Development and Design Transfer in the medical device industry or equivalent.
Certification in Six Sigma Black Belt or Green Belt

Required Knowledge, Skills and Abilities

Hands-on experience with process validation (IQ/OQ/PQ), risk management (FMEA), and statistical analysis.
Proficiency with CAD tools (SolidWorks, Creo), GD&T, and tolerancing methods.
Strong problem-solving skills with familiarity in DOE, SPC, and root-cause methodologies.
Knowledge of polymer processing, metal fabrication, laser welding or additive manufacturing.
Experience in Audit Readiness and Internal/External Audits with the various Regulatory bodies (FDA, TGA, PMDA, etc.)
Ability to communicate within the discipline and with others who are not technically trained
Ability to prioritize tasks in a fast-paced environment.

Supervision/Management Of Others:
Intern, Co-op, Engineer I and/or II

Internal and External Contacts/Relationships

Interacts with others in and across departments/sites and external contacts (suppliers, test laboratories)

Environmental/Safety/Physical Work Conditions

Responsible for understanding and conforming with the Environmental Policy to ensure that significant environmental aspects that relate to actual or potential impacts with their work are executed to minimize the effects on the environment.
Responsible for bringing to the attention of management any potential improvements that could reduce our environmental impact or to report activities that could result in a negative impact to the environment.
Responsible for understanding and conforming with the Health and Safety Policy to ensure that the significant risks that relate to actual or potential hazards with their work are identified.
Must be capable of performing system level testing at the home office or at outside labs.
Involves sitting 60% of the time, walking 20% and standing 20%.
Work is performed in an office 35% of the time, engineering lab 45%, and at an outside test lab 20%.
Work in the office environment involves use of a personal computer 80% of the time with the remainder spent conferring with colleagues and reviewing other documents.

The salary range for this position is between $115,000 and $135,000 per year depending on experience.

#LI-MV1

About us

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.

Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:

Health, Dental, and Vision insurance benefits
401k plan with company match
Paid Time Off
Wellness initiative & Health Assistance Resources
Life Insurance
Short and Long Term Disability Benefits
Health and Dependent Care Flexible Spending Accounts
Commuter Benefits
Parental and Caregiver Leave
Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

Apply Now

Refine Your Search

sr. engineer, process development wayne, nj jobs in new jersey

Sr. Engineer, Process Development - Wayne, NJ

DRUG SAFETY ASSOCIATE (multiple openings)

Integration Analyst

Family Medicine Physician

Spanish Teacher

NP

Litigation Attorney

Primary Care Physician - New Grads Preferred

Land Use Attorney

Nursing Clinical Coordinator

Pain Management & Regenerative Medicine Physician (MD)

Clinical Supervisor

Outside Sales Representative

Criminal Defense Attorney

Primary Care / Sports Medicine Physician (MD or DO)

Orthopedic Surgeon

SLP / Speech Language Pathologist - Home Health

Arbitration Relations Counsel (Attorney)

Physician Assistant

Physical Therapist - Outpatient Orthopedics

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