KIK Custom Products

  • Quality Assurance Supervisor

    Job Location US-IN-Elkhart
    Posted Date 1 week ago(6/11/2018 4:27 PM)
    Job ID
    # of Openings
  • Overview

    Custom New Logo

    Company Overview

    KIK has over 5,000 employees and operates 29 manufacturing facilities strategically located throughout North America. KIK has 2 Divisions, this position is in the KIK Custom Manufacturing, "KCM" Division.


    KCM Division leading contract manufacturer of personal care and over the counter drug products in North America, serving over 100 CPG companies, including many of the leading players. Each year, approximately one billion units representing thousands of different consumer products leave our plants destined for North American households. Our multi-product manufacturing and packaging capabilities include an extensive portfolio of aerosol, liquid, gel and cream products, among others. For example, KCM fills approximately 25% of all home and personal care aerosol products in the United States


    Position Summary

    The Quality Assurance Supervisor is responsible for managing and overseeing activities of quality inspectors in production including scheduling, assigning roles and responsibilities, ensuring all samples are pulled from production, maintaining a regulatory presence and ensuring all shifts have approrpiate coverage.  Train, direct and lead 10 quality inspectors across the 3 shifts on the production lines at the Main plant. This position is on second shift.  Hours for second shift 3 PM - 11 PM.

    Essential Job Functions

    • Responsible for supervising QA functions at KIK.
    • Coordinate special projects as requested.
    • Provide training, mentoring and supervision to Quality Assurance Inspectors
    • Continuously improve quality and  performance based on the key performance indicators
    • Interact with Specifications Department, Warehousing, Compounding, Lab and other departments as appropriate.
    • Conduct employee SOP training  and ensure training effectiveness
    • Communicate safety topics, quality procedures and updates.
    • Direct and advise auditors in the execution of rework protocols
    • Assure Line audits are conducted and retain samples pulled for all production.
    • Responsible for monitoring cGMP’s.


    • Minimum two-year degree/trade school/certification or significant experience in area of discipline required
    • Supervisory experience, able to work independently making decisions on personnel and staff issues
    • Quality Assurance experience in a FDA manufacturing environment
    • Good people skills
    • Attention to detail and organized, good time manager
    • Advanced experience in MS Office, Excel, Word, etc.




    Thank you for your interest and consideration of a career with KIK!

    KIK is an Equal Opportunity / Affirmative Action employer.

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