Injection Molding Process Engineer

Johnson & Johnson

Materials Engineer leading raw material and molding projects for inter-ocular lenses at Johnson & Johnson. Collaborating with cross-functional teams in an FDA-regulated medical device environment.

Posted 7/30/2026full-timeAnasco • Florida • 🇺🇸 United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading projects related to the manufacture of inter-ocular lenses, with a strong focus on risk assessment, process validation, and collaboration across multi-functional teams. Proficient in utilizing AutoCad/Inventor and experienced in FDA-regulated environments, ensuring quality and compliance in project execution.

Highest-signal resume keywords

Project ManagementRisk AssessmentAutoCad/Inventor ProficiencySix Sigma AccreditationFDA-Regulated Industry Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementRisk AssessmentProcess ValidationMicro-MoldingMold DesignInjection MoldingContinuous ImprovementBudget ManagementQuality AssuranceSupplier Coordination

Soft Skills

Excellent Communication SkillsInterpersonal SkillsTeam CollaborationLeadership

Certifications & Qualifications

Six Sigma Green BeltSix Sigma Black Belt

Industry Keywords

Inter-Ocular LensesFDA-RegulatedMedical DevicePharmaceuticalsMaterials SciencePlastics EngineeringMechanical Engineering

About the role

Key responsibilities & impact

Lead multiple raw material and molding related projects for the manufacture of inter-ocular lenses (IOL)
Lead multi-functional project teams and ensure that projects are completed on time and within budget
Collaborate with key business partners including Procurement, R&D, Supplier Quality, Engineering, Operations, Quality Assurance, and Regulatory Affairs
Act as an advocate for continuous improvement of technology and processes, minimizing lifecycle costs, and adhering to environmental policies and procedures
Conduct risk assessments and leading detailed product/process design reviews
Develop project and qualification plans to lead projects to meet timelines and budgets
Responsible for identifying, coordinating, planning, executing, and evaluating value improvement projects at key materials suppliers to ensure quality, and on-time delivery

Requirements

What you’ll need

Minimum of a Bachelor’s degree in Plastics Engineering, Mechanical Engineering, Materials Science or equivalent engineering
Relevant work experience is required
Ability to use and navigate AutoCad/Inventor is highly desirable
Candidate must speak fluent English
Excellent written and oral communication skills required
Excellent interpersonal skills required
Achievement of Six Sigma/Green Belt/Black Belt accreditation is preferred
Experience/familiarity with an FDA-regulated medical device or pharmaceuticals industry is preferred
Experience qualifying (Validation & Risk Assessments) materials or processes in automated manufacturing environment is desirable
Experience with micro-molding, mold design or overall injection molding is preferred
Working experience with external suppliers to include partnering internationally is preferred

Benefits

Comp & perks

Inclusive work environment
Health insurance
Professional development opportunities