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Lead Manufacturing Assembler

Getinge

Wayne, NJOnsitePosted 10 days ago$27.00 - $31.00/hour
Full TimeSenior LevelManufacturing & CMCMedical Device
Original posting ↗

Summary

In a team environment, oversee all workflow for a team or teams. Assists supervisor in the achievement of daily production schedules and quality goals. Responsible for training, scheduling workflow, accurate documentation and assisting team members with problems. Assist engineers or area supervision in development and support of the introduction of new processes and/or products.

Job description

Job Overview

In a team environment, oversee all workflow for a team or teams. Assists supervisor in the achievement of daily production schedules and quality goals. Responsible for training, scheduling workflow, accurate documentation and assisting team members with problems. Assist engineers or area supervision in development and support of the introduction of new processes and/or products.

Job Responsibilities and Essential Duties

  • Understands, adheres to, and promotes safety policies and practices.
  • Responsible for quality and adheres to manufacturing process requirements, Quality Policy and the Strategic Quality Process (SQP).
  • Proactively identifies and communicates quality issues and concerns; actively pursues resolution of issues by utilizing all resources.
  • Responsible for coordination and prioritization of production and/or pilot build schedules, NCMRs reworks, and determines the ability to meet the requirements.
  • Assist the supervisor in supporting and developing action plans to achieve departmental goals.
  • Establishes relationships and acts as a liaison to proactively communicate between all cross-functional teams by utilizing effective written and verbal communication skills.
  • Collaborates cross-functionally to plan, in advance, resources and supplies in order to meet business needs.
  • Must have working knowledge of all processes in the assigned area.
  • Builds product as necessary by following all processes in which certified (in their most current revision), while meeting manufacturing goals and metrics.
  • Demonstrates, promotes, and suggests ideas for Lean Manufacturing and other continuous improvement initiatives.
  • Takes an active leadership role in developing and driving Lean activities, including Born Lean strategies.
  • Maintains accurate records, including shop floor paperwork (SFP), work requests, and site-specific documentation.
  • Consistently monitors team records to ensure accuracy.
  • Understands and ensures compliance of MCA and site-specific policies and procedures.
  • Responsible for attending and passing all required MCA and site-specific training (i.e., QS Basics, Lean Training).
  • Responsible for performing shelf-life inspection and tracking of inventory items that have a defined shelf-life, maintaining the chemical expiration log and checklist, and the Periodic Torque Asset Verification Process.
  • Responsible for verification of the daily equipment log sheet.
  • Responsible for the verification of the incomplete assembly/sub-assembly/test tags at the end of each day.
  • Ability to perform basic SAP transactions (block material, complete WO using transactions (CO15, MIGO GR), transferring rejects to QCRI, and scrapping defective components).
  • Ability to close work orders in SAP every week.
  • Responsible for WO label creation and reconciliation of their corresponding areas.
  • Provides input to performance appraisals.
  • Ability to compile monthly information and create the diverted hours financial report and the daily production update report.
  • Assist the Production Supervisor in the operation of the manufacturing area and provide direction when the Production Supervisor is not available.
  • Acts as liaison between manufacturing and other departments, such as engineering and facilities, to communicate needs or make requests.
  • Maintains accurate records, including DHRs. Consistently ensures the team maintains records accurately.

Minimum Requirements

  • High school or equivalent required and 5+ years of work experience, or 6 years of work experience required.
  • Minimum of 3-4 years in a medical device or other regulated manufacturing environment.
  • AA degree preferred.

Required Knowledge, Skills, and Abilities

  • Demonstrated ability to follow processes, has an extensive understanding of the technical job duties and their practical applications to complex problems and situations.
  • Demonstrates proficiency in all communication, including written and spoken, as well as strong math skills.
  • Must be proficient in job-related computer programs or databases i.e., SAP, MS Office.
  • Must demonstrate ability to work effectively in a team setting, be flexible, and exhibit a willingness to learn/take on new tasks.
  • Must demonstrate the ability to work under limited supervision and assist with the training and coaching of others.

Supervision/Management of Others

Provide direction for Sr. Product Assemblers and Assemblers.

Requirements

  • High school diploma or equivalent required
  • 5+ years of work experience, or 6 years of work experience
  • Minimum of 3-4 years in a medical device or other regulated manufacturing environment
  • AA degree preferred
  • Demonstrated ability to follow processes
  • Extensive understanding of technical job duties and practical applications to complex problems
  • Proficiency in written and spoken communication
  • Strong math skills
  • Proficiency in SAP
  • Proficiency in MS Office
  • Ability to work effectively in a team setting
  • Flexibility and willingness to learn/take on new tasks
  • Ability to work under limited supervision
  • Ability to assist with training and coaching of others

Benefits

  • Health, Dental & Vision Insurance
  • 401(k) Matching
  • Paid Time Off
  • Wellness Initiative
  • Health Assistance Resources
  • Life Insurance
  • Short & Long Term Disability
  • Flexible Spending Accounts
  • Commuter Benefits
  • Parental & Caregiver Leave
  • Tuition Reimbursement
  • Excellence Incentive Plan

Company overview

Getinge AB is a leading Swedish medical technology company founded in 1904 and headquartered in Gothenburg, Sweden. As a publicly traded company listed on Nasdaq Stockholm, Getinge specializes in developing and manufacturing advanced medical devices and solutions for healthcare and life sciences industries. The company operates through three core business areas: Life Science, Acute Care Therapies, and Surgical Workflows. Getinge's comprehensive product portfolio includes ventilators, heart-lung machines, anesthesia systems, surgical tables, sterilizers, washer-disinfectors, bioreactors, and digital health solutions. With approximately 12,000 employees worldwide, operations in 40 countries, and sales in over 135 countries, Getinge has established itself as a global leader in medical technology. The company maintains manufacturing facilities across Europe, Asia, and North America, with the United States representing its largest market. Getinge's commitment to innovation and patient safety has made it a trusted partner for hospitals, research laboratories, and pharmaceutical production facilities worldwide, dedicated to improving clinical outcomes and optimizing healthcare workflows.

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