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Quality System Specialist

Job in Greendale, Milwaukee County, Wisconsin, 53129, USA
Listing for: Adecco
Full Time, Seasonal/Temporary position
Listed on 2026-01-01
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 30 - 35 USD Hourly USD 30.00 35.00 HOUR
Job Description & How to Apply Below

Light Industrial Position

Job Title:

Quality System Specialist (Temp-to-Hire)

Requirements:
Steel toe shoes

Pay: $30-$35/hour

Schedule:

Monday–Friday, 8 hours/day (start time 7:00, 8:00, or 9:00 AM)

Position Summary

A temp-to-hire Quality System Specialist is needed to join the Quality Assurance team at the Greendale, Indiana site. This role is critical to the integrity and continuous improvement of the 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 Track Wise.

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., Track Wise or similar).

Specific Tasks, Duties, and 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 with quality system updates.

Computerized System Compliance

  • Support Data Integrity initiatives for electronic systems including Track Wise, 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.
Essential Skills, Experience, and Qualifications

Required:

  • 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 Track Wise and/or EDMS or equivalent.
  • Lean Six Sigma or similar continuous improvement training.
  • Project Management experience.
Pay Details

$30.00 to $35.00 per hour

Benefits

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal

Opportunity Employer / Veterans / Disabled

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to

  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance

Massachusetts Candidates Only:
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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