Jobs in the United States

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Added 1 hour ago
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Mechanical Manufacturing Engineer
GPAC
Torrington, CT
- $85,000 to $120,000 USD / year
…molded parts is hiring a hands-on Mechanical Manufacturing Engineer to support new product introduction, product launches, and ongoing production, spending real time on the floor solving…
Added 1 hour ago
Engineer
J&J Family of Companies
Jacksonville, FL
…Execution Focus, Facility Management, Good Manufacturing Practices (GMP), Lean Manufacturing Principles, Lean Supply Chain Management, Manufacturing Engineering, Manufacturing Science and…
Added 2 hours ago
Sr. Automation Engineer
Phantom Staffing
Greenfield · Greenfield, IN
…including coordinating cross functional teams in support of this…
Added 2 hours ago
Senior Manufacturing Systems Engineer - PLC Systems
Amgen
Holly Springs, NC
Direct knowledge of Automation System design, experience in Process control engineering and troubleshooting with GMP biopharmaceutical production facility equipment/systems automation.
Added 2 hours ago
Staff Validation Engineer, Media Fills
ThermoFisher Scientific
Greenville, NC
…work that makes a positive impact on a global scale. The Staff Engineer, Media Fill plays a critical role in supporting sterile/aseptic manufacturing operations by leading media fill…
Added 6 hours ago
Sr Engineer - Process Development
Illumina, Inc.
CA
The estimated base salary range for the Sr Engineer - Process Development role based in the United States of America is: $98,400 - $147,600. Should the level or location of the role change…
Added 6 hours ago
Sr. Process Engineer
PCI San Diego, Inc.
San Diego, CA
Advanced understanding of GMP regulations and requirements
Added 7 hours ago
Associate Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing (Onsite)
Merck
Rahway, NJ
The Oral Solids Dosage (Non-Sterile) team at the FLEx Center in Rahway is looking for an Associate Specialist – Process Engineer to lead clinical supply manufacturing, scientific rigor of…
Added 8 hours ago
Engineer I - Engineering, Validation
Catalent Pharma Solutions LLC
Madison, WI
…Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical…
Added 8 hours ago
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Lead Facilities Technician
Quality Agents
Gaithersburg, MD
- $40 to $49 USD / hour
Hands-on experience with GMP mechanical, electrical and HVAC systems and with clean utilities (purified water, WFI, clean steam, compressed air, process gases).
Added 8 hours ago
Maintenance Supervisor
The Cheesecake Factory Inc.
Battleboro, NC
Enforce maintenance standard work, safety practices, and GMP compliance.
Added 9 hours ago
Senior Engineer - Utilities & Systems/Automation Integration
Amgen Manufacturing Limited LLC
United States
…role provides engineering expertise across utilities systems, process monitoring, and systems integration, supporting reliability, operational efficiency, and regulatory…
Added 9 hours ago
Engineer III/Sr. Engineer I, Manufacturing Sciences – Drug Product
Biogen
Research Triangle Park, NC
The Engineer III/Sr. Engineer I, Manufacturing Sciences serves as a key scientific and technical resource supporting aseptic drug product manufacturing at Biogen’s RTP Pharma facility. This…
Added 9 hours ago
Staff Manufacturing Test Engineer
ZMC-US CMS ZOLL Manufacturing Corporation
Pittsburgh, PA
Work in a team environment to provide manufacturing test input to process flow diagrams, process FMECAs, process characterizations, and process validation protocols and reports.
Added 9 hours ago
QA
Facilities Technician
Quality Agents
Gaithersburg, MD
- $34 to $42 USD / hour
Hands-on experience with GMP mechanical, electrical and HVAC systems. Experience with clean utilities (purified water, WFI, clean steam, compressed air, process gases) is strongly desired.
Added 10 hours ago
Electrical Design Engineer
Amron Internation Diving Supply
Vista, CA
Amron is hiring a full-time Electrical Design Engineer for the design and development of miscellaneous electronic products with an emphasis on analog/digital communication/intercom…
Added 10 hours ago
RD
MES Application & Integration Expert
Roche Diabetes Care, Inc.
United States
- $85,000 to $157,800 USD / year
We are seeking a proactive and skilled MES Engineer with 4+ years of experience to support, configure, and integrate Manufacturing Execution Systems within our production facility. In this…
Added 10 hours ago
Sr. Engineer, Automation Engineering, Controls Hardware - Lilly Medicine Foundry
Eli Lilly and Company
United States
The Senior Engineer - Automation Engineering will work as a member of the Automation Engineering Department at Eli Lilly, Foundry. The engineer will provide automation support for one or…
Added 11 hours ago
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Manufacturing Quality Engineer
Actalent
Mechanicsburg, PA
- $70,000 to $90,000 USD / year
Job Title: Quality EngineerJob DescriptionWe are seeking a detail-oriented Quality Engineer with a passion for improving manufacturing processes. The ideal candidate will have extensive…
Added 11 hours ago
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Facilities Engineer
Synthego
Redwood City, CA
- $110,000 to $130,000 USD / year
Synthego is seeking an experienced and technically driven Facilities Engineer to support the operation, maintenance, troubleshooting, and continuous improvement of critical facility…
Added 11 hours ago
Senior Development Quality Engineer
St. Jude Medical, Cardiology Division, I
CA
The Senior Development Quality Engineer assures new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a…
Added 12 hours ago
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Process Engineer II, Manufacturing Process Validation & Equipment Qualification
Lantheus Brand
Springfield, NJ
- $148,000 USD / year
We are seeking a Process Engineer II who will be responsible for providing technical support for pharmaceutical and radiopharmaceutical manufacturing operations throughout the product…
Added 12 hours ago
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Quality Engineer
Actalent
Phillipsburg, NJ
- $40 to $45 USD / hour
Job Title: Quality EngineerJob DescriptionThe Quality Engineer plays a key role in ensuring that medical device products and processes comply with FDA 21 CFR 820, ISO standards, and…
Added 12 hours ago
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Process Engineer
Actalent
Scottsdale, AZ
- $100,000 to $130,000 USD / year
Process Engineer IIIJob DescriptionThe Level 3 Process Engineer plays a critical role in developing, validating, and optimizing manufacturing processes for medical devices in a regulated…
Added 12 hours ago
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SENIOR MECHANICAL ENGINEER
GPAC
Saint Louis, MO
- $120,000 to $160,000 USD / year
Proven success managing large, complex HVAC, plumbing, piping, or process mechanical projects

Actalent

Quality Engineer

Phillipsburg, NJ, United States

$40 to $45 USD / hour

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Job details

Pay: $40 to $45 USD / hour
Posting language: English
Posted: Nov 6, 2026

Original job description

Job Title: Quality EngineerJob DescriptionThe Quality Engineer plays a key role in ensuring that medical device products and processes comply with FDA 21 CFR 820, ISO standards, and international medical device regulations. This position focuses on managing quality systems activities, including sterilization qualification, CAPA management, validation review, and maintaining documentation needed for audits. The role requires strong organizational skills, attention to detail, and the ability to drive quality improvements across the organization.

Responsibilities

Ensure compliance with FDA 21 CFR 820, Quality System Regulations (QSR), Good Manufacturing Practices (GMP), ISO standards, and international medical device regulations (including MDR) in assigned areas.
Understand and support sterilization qualification and ongoing maintenance activities as they relate to medical devices.
Manage the corrective and preventive action (CAPA) process from initial investigation through implementation and effectiveness checks.
Maintain Design History Files and Technical Files, ensuring documentation is complete, accurate, and ready for internal and external audits.
Organize and prioritize assigned tasks to ensure projects meet expectations, milestones, and timelines.
Create, deliver, and maintain department and company training related to quality systems, procedures, and regulatory requirements.
Review and approve verification and validation protocols and reports to ensure they meet regulatory and company standards.
Utilize quality tools such as Failure Modes and Effects Analysis (FMEA), Control Plans, and Process Flow diagrams to support risk management and process improvement.
Support and maintain the medical device Quality Management System (QMS), including ISO-related activities and documentation.
Collaborate with cross-functional teams to resolve quality issues and implement sustainable corrective actions.
Prepare for and participate in internal and external audits by providing required quality and regulatory documentation.

Essential Skills

Relevant quality engineering work experience in an ISO-regulated medical device environment.
Demonstrated experience reviewing verification and validation protocols and reports.
Proven ability to manage CAPA processes from investigation through effectiveness checks.
Experience supporting and maintaining medical device Quality Management System (QMS) activities.
Knowledge of FDA 21 CFR 820, QSR, GMP, ISO standards, and international medical device regulations (including MDR).
Understanding of sterilization qualification and maintenance for medical devices.
Proficiency with quality tools such as FMEA, Control Plans, and Process Flow diagrams.
Bachelors degree in Engineering or a related field of study.
Proficiency in Microsoft Excel, Word, and other common office software.
Strong verbal and written communication skills in English.
Ability to stand, sit, and work at a computer for normal periods.

Additional Skills & Qualifications

Experience working within a laid-back, collaborative, and team-oriented environment.
Ability to organize and prioritize multiple tasks to meet project deadlines.
Comfort collaborating across departments to support training and continuous improvement initiatives.
Strong attention to detail and commitment to maintaining accurate and audit-ready documentation.

Work EnvironmentThis is a fully onsite position, Monday through Friday, typically from 8:00 a.m. to 5:00 p.m., with some flexibility in hours depending on employee needs. The company culture is laid-back and family-like, with a tight-knit group that values collaboration and open communication. Leadership maintains an open-door policy and fosters a welcoming environment. The team regularly engages in fun activities outside of work, promoting strong relationships and a positive atmosphere. Work is primarily performed in an office setting, involving regular standing or sitting and working at a computer for normal periods, with standard business-casual attire appropriate for a professional environment. Job Type & LocationThis is a Contract to Hire position based out of Phillipsburg, NJ. Pay and BenefitsThe pay range for this position is $40.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract to Hire position based out of Phillipsburg, NJ. Application DeadlineThis position is anticipated to close on Nov 20, 2026. Workplace TypeThis is a fully onsite position in Phillipsburg,NJ.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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More about this job

Skills

Organizational skills
Attention to detail
Regulatory compliance
Good manufacturing practices
Medical device regulations
Medical devices
Documentation
Quality control systems
Risk management
Process improvement
Quality assurance procedures
Microsoft Excel
Microsoft Word
Office software
Communication skills
Collaboration
Leadership

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