73 applicants

Company

Original Job Post

Getinge · 2 days ago

Engineer II, Production

Wayne, NJ

Full-time

Onsite

Mid, Senior Level

$88K/yr - $95K/yr

3+ years exp

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Responsibilities

Works cross-functionally as a team member to design and develop breakthrough process technologies for the manufacture of new medical devices.

Ensures the efficient and effective commercialization and transfer of new products into production.

Supports manufacturing area in tooling design, process improvement, and cost improvement.

Works with and assists senior members of Engineering Group to implement new products and performance enhancements and quality of existing products.

Executes the functional deliverables associated with the Technology Product Development Processes, Project Management, and Quality Systems under the direction of senior engineering staff.

Leads small projects that support product enhancement and cost savings opportunities.

Participates in a team environment to enhance processes and product performance.

Assists in evaluating and developing internal and external process technologies.

Assists in the design and development of machines and mechanisms for the manufacture of new and existing products.

Performs development studies and prototyping to verify processing concepts and help define manufacturing systems.

Develops processes, methods, tooling and production controls for new programs; supervises their assembly and proofing.

Prepares technical reports, analysis, recommendations and presentations reflecting the status and results of projects in progress on a regular basis.

Sets up new equipment, assures compliant operation, and prepares Manufacturing Work Instructions for use.

Prepares and updates Manufacturing Work Instructions based on process improvements, equipment implementation, and design/product changes.

Drafts protocols and manages all phases of process validations and equipment validations.

Prepares capital appropriation requests providing required evaluation, analysis, and supporting justification.

Qualification

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Project managementEngineering principlesPrototype developmentProduction processesDocumentationRisk managementStatistical techniquesDesign of ExperimentsTest Method ValidationCorrective & Preventative ActionMS OfficeComputer Aided DesignMinitabGoal orientedTeam playerAttention to detailWritten communicationVerbal communicationProblem solverSix Sigma Green Belt

Required

BS or MS in Biomedical, Mechanical or Industrial Engineering, or equivalent, with at least 3 - 6 years related experience

Goal oriented team player (individual contributor, project team member); works with very general instruction exhibits attention to detail, works to schedules, and possesses good written and verbal communication skills

Demonstrates the ability to lead low to moderate complexity design change projects and initiatives

Trainer; technicians, inspectors, operators

Utilizes a range of Engineering principles (analytical, mathematical)

Prototype/production processes; fixtures, tooling, equipment development and related assembly processes and inspection methods

Documentation; bill of materials, drawings, specifications, protocols, test methods, work instructions

Risk Management - design/process FMEA development

Statistical techniques, Design of Experiments (DOE)

Test Method Validation (GRR – Minitab)

Corrective & Preventative Action - creative problem solver; assess problems, implement timely and effective solutions

Computer proficient: MS Office suite (Excel, Explorer, Outlook, PowerPoint, Project, Visio, Word)

Computer Aided Design (SolidWorks)

Statistical Techniques (Minitab)