Johnson & Johnson

Process Engineer II

Johnson & Johnson$65K — $104K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering or equivalent technical discipline.
  • 2-4 years of engineering experience in manufacturing or related environments.
  • Experience in a regulated industry such as Medical Device or Pharmaceutical.
  • Strong analytical, problem-solving, and decision-making skills.
  • Ability to conduct process evaluations and data analysis.
  • Strong communication and interpersonal skills.
  • Proficiency with Microsoft Office applications.

Responsibilities

  • Support the optimization of manufacturing processes and equipment.
  • Conduct process characterization and capability studies to enhance performance.
  • Research and evaluate emerging technologies for process improvement.
  • Collaborate on engineering projects related to manufacturing support activities.
  • Provide manufacturability feedback during design reviews with cross-functional teams.
  • Define requirements for safe and compliant product manufacturing.
  • Identify continuous improvement opportunities by analyzing processes and equipment.

Benefits

  • Opportunities for professional development and career advancement.
  • Access to comprehensive health and wellness programs.
  • Participation in a collaborative and innovative work environment.
  • Potential for flexible work arrangements as company policies evolve.
Full Job Description
Job Function:
Supply Chain Engineering

Job Sub Function:
Process Engineering

Job Category:
Scientific/Technology

All Job Posting Locations:
Massachusetts (Any City), Raynham, Massachusetts, United States of America

Job Description:

Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

DePuy Synthes (DPS) is recruiting for a Technician within the Joints Platform - Manufacturing Innovation team. This role will be located in Raynham, MA.

DePuy Synthes, the Orthopedics Company of Johnson & Johnson provides one of the most comprehensive orthopedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit www.depuysynthes.com.

The Process Engineer is responsible for providing engineering and process controls support to manufacturing operations through the development, optimization, validation, and implementation of manufacturing processes. This role partners cross-functionally with Operations, Quality, Engineering, and Supply Chain teams to improve process capability, product quality, efficiency, and cost performance.

The Process Engineer applies engineering principles, statistical analysis, problem-solving methodologies, and continuous improvement tools to support new product introductions, process validations, equipment implementation, and manufacturing optimization initiatives. This position plays a key role in evaluating new technologies, conducting process characterization studies, and implementing sustainable solutions that enhance operational performance in a regulated manufacturing environment.

Key Responsibilities
  • Support the development, implementation, and optimization of manufacturing processes, equipment, and controls to improve quality, efficiency, and operational performance.
  • Conduct process characterization, capability studies, designed experiments (DOE), and data analysis to improve process understanding and performance.
  • Research current and emerging technologies and evaluate alternatives related to process capability, quality, and cost.
  • Participate in engineering projects involving process improvements, new product introductions, equipment implementation, and manufacturing support activities.
  • Provide manufacturability feedback through design reviews and collaboration with cross-functional teams.
  • Define process, equipment, and material requirements to ensure products are manufactured safely, efficiently, and in compliance with quality standards.
  • Evaluate and select manufacturing equipment and technologies to support operational objectives and future business needs.
  • Coordinate vendor evaluations, equipment trials, and technology assessments.
  • Develop, execute, and support process validation activities and capability assessments.
  • Analyze manufacturing processes and equipment performance to identify opportunities for continuous improvement.
  • Develop and maintain process specifications, work instructions, training materials, and technical documentation.
  • Support troubleshooting efforts through root cause analysis, corrective actions, and implementation of sustainable solutions.
  • Collaborate with Operations, Quality, Maintenance, and Engineering teams to improve manufacturing performance and compliance.
  • Support compliance with quality systems, safety regulations, and company procedures.


Required Skills
  • Bachelor's Degree in Engineering or equivalent technical discipline.
  • 2-4 years of engineering experience in manufacturing, process engineering, operations, or a related technical environment.
  • Experience working in a regulated industry such as Medical Device, Pharmaceutical, Healthcare, or similar manufacturing environment.
  • Strong analytical, problem-solving, and decision-making skills.
  • Ability to conduct process evaluations, data analysis, and technical investigations.
  • Strong communication and interpersonal skills with the ability to work effectively in a team environment.
  • Ability to collaborate with multiple functions and levels of leadership.
  • Knowledge of engineering principles, process development, and manufacturing operations.
  • Proficiency with Microsoft Office applications, including Excel, Word, PowerPoint, and Outlook.


Preferred Skills
  • Experience in Medical Device manufacturing or other highly regulated industries.
  • Knowledge of Geometric Dimensioning & Tolerancing (GD&T).
  • Experience with process validation activities and manufacturing qualifications.
  • Knowledge of statistical analysis tools such as Minitab or similar software.
  • Experience with Design of Experiments (DOE), process characterization, and capability studies.
  • Project management experience supporting engineering or manufacturing initiatives.
  • Knowledge of Lean Manufacturing, Six Sigma, Process Excellence, or Continuous Improvement methodologies.
  • Experience supporting equipment selection, qualification, and implementation projects.
  • Familiarity with quality systems, GMP requirements, and manufacturing compliance standards.
  • Green Belt or equivalent continuous improvement certification preferred.


Required Skills:

Preferred Skills:
Analytical Reasoning, Computerized Equipment Skills, Corrective and Preventive Action (CAPA), Emerging Technologies, Execution Focus, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Process Control, Process Engineering, Process Oriented, Product Improvements, Project Engineering, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Technical Research, Technologically Savvy

The anticipated base pay range for this position is :
$65,000.00 - $104,650.00

Additional Description for Pay Transparency:

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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