×
Register Here to Apply for Jobs or Post Jobs. X

Quality Management Systems Specialist

Job in Greendale, Dearborn County, Indiana, USA
Listing for: Ampcus, Inc
Full Time position
Listed on 2026-01-01
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Job Description & How to Apply Below
Location: Greendale

Job Title

Quality Management Systems Specialist

Location

Greendale, IN

Position Summary

We are seeking a Quality Management Systems Specialist to join our dynamic Quality Assurance team at our 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 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).

Key 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 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.
Required Qualifications and Experience
  • 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.

Ampcus is an Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veterans or individuals with disabilities.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary