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Johnson & Johnson

Process Engineer II

Johnson & Johnson

. Provide engineering and process controls support to manufacturing operations through development, optimization, validation, and implementation of manufacturing processes .

Posted 9/17/2026full-timeRaynham • Massachusetts • United StatesJuniorMid-Level💰 $65,000 - $104,650 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in process engineering, optimization, and validation within regulated manufacturing environments, with a strong focus on continuous improvement and compliance with quality systems. Proficient in data analysis, technical documentation, and cross-functional collaboration to enhance manufacturing operations.

Highest-signal resume keywords
Process EngineeringProcess ValidationData AnalysisLean ManufacturingSix Sigma

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Process DevelopmentManufacturing OperationsDesign of Experiments (DOE)Geometric Dimensioning & Tolerancing (GD&T)Statistical AnalysisContinuous ImprovementRoot Cause AnalysisCapability StudiesTechnical InvestigationsEquipment Qualification
Soft Skills
Analytical SkillsProblem-SolvingDecision-MakingCommunication SkillsInterpersonal Skills
Tools & Technologies
Microsoft OfficeMinitabQuality SystemsGMP Requirements
Certifications & Qualifications
Green Belt
Industry Keywords
Medical DevicePharmaceuticalHealthcareRegulated IndustryManufacturing Compliance

About the role

Key responsibilities & impact
  • Provide engineering and process controls support to manufacturing operations through development, optimization, validation, and implementation of manufacturing processes
  • Support development, implementation, and optimization of manufacturing processes, equipment, and controls
  • Conduct process characterization, capability studies, designed experiments (DOE), and data analysis
  • Research current and emerging technologies and evaluate alternatives related to process capability, quality, and cost
  • Participate in process improvement, new product introduction, equipment implementation, and manufacturing support projects
  • Provide manufacturability feedback through design reviews and cross-functional collaboration
  • Define process, equipment, and material requirements
  • Evaluate and select manufacturing equipment and technologies
  • Coordinate vendor evaluations, equipment trials, and technology assessments
  • Develop, execute, and support process validation activities and capability assessments
  • Analyze process and equipment performance to identify continuous improvement opportunities
  • Develop and maintain process specifications, work instructions, training materials, and technical documentation
  • Support troubleshooting through root cause analysis, corrective actions, and sustainable solutions
  • Collaborate with Operations, Quality, Maintenance, and Engineering teams
  • Support compliance with quality systems, safety regulations, and company procedures

Requirements

What you’ll need
  • 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
  • Experience in Medical Device manufacturing or other highly regulated industries preferred
  • Knowledge of Geometric Dimensioning & Tolerancing (GD&T) preferred
  • Experience with process validation activities and manufacturing qualifications preferred
  • Knowledge of statistical analysis tools such as Minitab or similar software preferred
  • Experience with Design of Experiments (DOE), process characterization, and capability studies preferred
  • Project management experience supporting engineering or manufacturing initiatives preferred
  • Knowledge of Lean Manufacturing, Six Sigma, Process Excellence, or Continuous Improvement methodologies preferred
  • Experience supporting equipment selection, qualification, and implementation projects preferred
  • Familiarity with quality systems, GMP requirements, and manufacturing compliance standards preferred
  • Green Belt or equivalent continuous improvement certification preferred

Benefits

Comp & perks
  • Anticipated employment and benefit plans through DePuy Synthes following the planned separation, subject to applicable processes and consultations
  • Inclusive work environment
  • Reasonable accommodation support for applicants with disabilities