Production Operator, 2nd Shift

Kimball Solutions Indianapolis, Inc.

Indianapolis (IN)

On-site

USD 22,000 - 33,000

Full time

4 days ago
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Benefits offered by this job

PTO & Holidays
Health Insurance
401(k) match
Bonus potential

Job summary

Kimball Electronics Indiana is seeking a Production Associate to assemble, test, and package parts per production procedures while documenting processes to meet quality, cost, and delivery goals in a medical device environment.

The role involves operating automated assembly equipment, reading procedures and drawings, and ensuring compliance with GMP/ISO-13485 and FDA regulations. 2nd shift with occasional overtime supports on-time delivery.

Qualifications

  • Attention to detail and good documentation skills.
  • Ability to read procedures and interpret assembly drawings.
  • Operate automated assembly equipment and hand tools with accuracy.
  • Maintain compliance with GMP/ISO-13485 and FDA requirements.

Responsibilities

  • Assemble parts per production procedures and BOMs.
  • Test and package finished products.
  • Document production activities according to procedures.
  • Maintain clean and safe working environment and follow 5S.

Skills

Attention to detail
Documentation skills
Read assembly drawings
Operate automated equipment
Team player

Tools

Manufacturing equipment

Job description

We are committed to providing reasonable accommodations for individuals with disabilities in our job application process. If you need assistance or an accommodation during the application or recruitment process due to a disability, you may contact us at KEIrecruiting@Kimballelectronics.com. We will treat all requests for accommodations discreetly. *Note: There is no Visa sponsorship being offered for this position. Kimball Electronics does not accept agency resumes. Please do not forward resumes to any recruiting alias or employee. Kimball Electronics is not responsible for any fees related to unsolicited resumes.

Benefits:
  • Kimball Medical Solutions provides 3 weeks of PTO starting your 1st year in addition to 10 paid holidays.
  • Potential monthly incentive bonus based on company performance.
  • Major health, dental, vision, and complementary insurances starting day 1.
  • We offer a 50% match on your first 6% of 401k contribution with opportunity for an employer contribution annually.

2nd Shift: 3p-11p M-F. Overtime when necessary.

Position Overview

The mission of the Production Associate is to assemble and pack parts per production procedures, and document production processes while meeting goals of quality, cost and delivery for our customers. This position reports to a Production Specialist within the Operations department of a growing Medical Device contract manufacturer focused on capital equipment, drug delivery devices and disposables.

Quick Summary

This position is responsible for assembly, testing, and packaging of finished products per production and quality system procedures using manufacturing machines and equipment, hand tools, custom fixtures, sub-assemblies, parts and fasteners. This includes the proper documentation of manufacturing activities according to production procedures and good manufacturing practices.

Basic Background Requirements
  • Attention to detail and good documentation skills
  • Ability to work on pharmaceutical products with the end patient in mind
  • Assemble simple devices with short cycle times and high daily volumes
  • Assemble complex devices with long cycle times and low daily volumes
  • Operate automated assembly equipment
  • Medical manufacturing experience is preferred
  • Operate equipment, fixtures and test stations per procedures and training.
  • Record results as defined by documentation.
  • Verification of work in accordance with checklists
  • Packaging and labeling of finished product into designated cartons per BOM
  • Ability to read procedures and interpret assembly drawings
  • Ability to stand, stoop, bend, reach and lift as required
  • Ability to analyze situations accurately and follow the applicable procedures
  • Able to work independently and as a member of a team
  • The ability to work with all levels of the organization
  • React to change productively and handle other tasks that may be assigned.
  • Ability to understand business, legal and regulatory requirements
  • Works overtime as required to provide excellent customer satisfaction
  • Maintain clean and safe working environment in accordance with company policies.
  • Maintain regular attendance according to the company’s attendance guidelines.
  • Maintain general knowledge of the certification and regulatory requirements contained in ISO-13485, and FDA CFR/GMP Medical Device Regulation
Key Performance Objectives
Short Term: (0 to 3 months)
  • Learn KEIND Quality system requirements
  • Learn Good Documentation Practices
  • Build relationships with Operations, Quality and Material Handling team members
  • Self-sufficient in several assembly and packaging jobs
  • Complete Work Orders per the assigned cycle times and schedule
  • Records complete and accurate information for Device History Records per Good Manufacturing Practices
  • Learn and adopt Kimball Electronics philosophies and culture
  • Maintain clean and safe working environment in accordance with company policies.
  • Maintain regular attendance according to the company's attendance guidelines.
  • Always works within Procedures
  • Works overtime as required
  • Report production in the ERP system and on Work Order paperwork
  • Learn KEIND Quality system requirements
  • Inspects work of previous operator when on a production line
  • Follow the 5S process for your area
Midterm: (3 to 6 months)
  • Complete inventory forms as required
  • Assist in work order setup
Long term: (6 to 12 months)
  • Provide training for other production associates on jobs which proficiency has been achieved
  • Provide improvement ideas for review
  • Complete Yellow Belt Training
Don’t meet every single requirement?

Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Kimball Electronics we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! We’re proud to be an equal opportunity employer and consider qualified applicants without regard to race, color, religion, sex, national origin, ancestry, age, genetic information, sexual orientation, gender identity, marital or family status, veteran status, medical condition or disability or any other characteristic protected by applicable federal, state, or local law. We will consider for employment qualified candidates with arrest and conviction records, consistent with applicable law (including, for example, the San Francisco Fair Chance Ordinance for roles based in San Francisco).

WHO WE ARE

Kimball Solutions was founded in 1961. We have established ourselves as a global leader in delivering durable electronics and offering contract manufacturing services for a wide range of industries. Our operations are supported by a robust Customer Relationship Management (CRM) model, which provides our customers with convenient access to our global footprint and services throughout the entire product life cycle. We are recognized for our commitment to quality, international standard certifications, financial stability, social responsibility, and long-term relationships, especially in industries that demand rigorous engineering controls and long product life cycles.

WHAT WE DO

We offer our services globally on a contract basis, manufacturing products to our customers’ specifications. Our comprehensive service offerings include:

  • Production and testing of printed circuit board assemblies (PCBAs)
  • High-level and final assembly of medical, automotive, and industrial products
  • Design services and support
  • Supply chain services and support
  • Rapid prototyping and new product introduction support
  • Product design and process validation and qualification
  • Industrialization and automation of manufacturing processes
  • Reliability testing (extreme environmental conditions)
  • Aftermarket services
  • Production and assembly of medical devices, medical disposables, and other non-electronic products
  • Drug delivery devices and solutions with and without electronics
  • Class 7 and 8 clean room assembly, cold chain, and product sterilization management
  • Design engineering and production of precision molded plastics
  • Complete product life cycle management
Our Package of Value

Our package of value begins with our core competency of producing durable electronics by providing Electronics Manufacturing Services (EMS), complemented by contract manufacturing services by our Contract Manufacturing Organization (CMO) for medical disposables, drug delivery solutions, and precision molded plastics. We combine our design and manufacturing expertise with highly integrated processes and procedures to deliver the highest levels of quality and reliability throughout the entire life cycle of our customers’ products. Our award-winning service, global operations platform, and dedication to standardization and teamwork ensure that we consistently meet and exceed our customers' expectations.

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