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Quality System Specialist
Quality System SpecialistAutomated Systems, Inc. • Greendale, WI, US
Quality System Specialist

Quality System Specialist

Automated Systems, Inc. • Greendale, WI, US
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Overview

Quality System Specialist — Contract to Hire : 6-month contract to hire role. Location : Greendale, IN - 100% Onsite. Shift : Mon-Fri, 8 hours a day starting at 7, 8 or 9am.

Automated Systems, Inc. is recruiting for a Quality Management Systems Specialist to join our client's dynamic Quality Assurance team at their Greendale, Indiana site. This role is critical to the integrity and continuous improvement of our site's Quality Systems and will be responsible for supporting key compliance and quality system activities such as entry of Change Controls, Deviations, Complaints, and CAPAs into TrackWise. The ideal candidate will bring an understanding of GMP principles, experience in pharmaceutical or dietary supplement manufacturing, and basic user knowledge of electronic quality systems (i.e. TrackWise or similar).

Responsibilities

  • Quality Systems Oversight : Support site-level quality systems such as Change Control and Deviation processes in accordance with internal procedures and regulatory expectations.
  • Ensure timely and thorough completion of assigned documentation tasks.
  • Support cross-functional teams quality system updates.
  • Computerized System Compliance : Support Data Integrity initiatives for electronic systems including TrackWise, EDMS, and other validated platforms.
  • Participate in system upgrades, validation activities, and periodic reviews to ensure ongoing compliance.

Documentation & Audit Support

  • Collaborate with Document Control and QA teams to ensure controlled documents are accurate, current, and compliant.
  • Support internal, client, and regulatory audits by preparing documentation as assigned.
  • Assist in batch record review / filing, complaint investigation initiation, and audit readiness activities as needed.

    • Requirements

  • 2+ years of experience in a GMP-regulated environment (pharmaceutical or dietary supplement preferred).
  • Experience with 21 CFR 111, 21 CFR 211, or 21 CFR 11.
  • Working knowledge of Quality Systems and Quality Assurance.
  • Experience with Microsoft Office Suite.
  • Excellent written and verbal communication skills.
  • Strong organizational and time management abilities.

    • Preferred

  • Experience with TrackWise and / or EDMS or equivalent
  • Lean Six Sigma or similar continuous improvement training
  • Project Management

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    Quality Specialist • Greendale, WI, US