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Associate Quality Systems Specialist

Job in Minneapolis, Hennepin County, Minnesota, 55400, USA
Listing for: Planet Pharma
Full Time position
Listed on 2026-10-15
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Engineering
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below

The Associate Quality Systems Specialist supports site closure activities by processing change orders, executing where-used assessments, coordinating documentation updates, and ensuring timely implementation of quality system changes in compliance with company procedures and regulatory requirements.

  • Process change orders associated with site closure and quality system inactivation activities.
  • Execute where-used assessments to identify impacted procedures, forms, specifications, records, and quality system documents.
  • Coordinate document updates and obsolescence activities required for site closure.
  • Support impact assessments and implementation of approved changes.
  • Track change order progress and ensure completion within established timelines.
  • Collaborate with cross-functional stakeholders including Quality, Operations, Engineering, Regulatory Affairs, and Document Control.
  • Maintain accurate records within the electronic Quality Management System (eQMS).
  • Support project reporting and status updates for site closure activities.
  • Ensure compliance with internal quality system requirements and applicable regulations.

Required Knowledge and Experience

  • Requires broad theoretical job knowledge typically obtained through advanced education.
  • Requires a Baccalaureate degree (or, for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A)).
  • 0 years of experience required

Preferred Qualifications

  • Internship, co-op, or academic project experience in Quality, Manufacturing, Engineering, Regulatory Affairs, or Document Control.
  • Experience working in a regulated environment such as Medical Device, Pharmaceutical, Biotechnology, or Manufacturing.
  • Familiarity with quality systems and document control processes.
  • Experience with electronic quality management systems (eQMS) is a plus.

Key Skills

  • Strong attention to detail.
  • Excellent organizational and time management skills.
  • Ability to manage multiple assignments and meet deadlines.
  • Strong written and verbal communication skills.
  • Proficient in Microsoft Office applications.
  • Ability to analyze information and identify document impacts across quality systems.
  • Ability to work independently and collaboratively within cross-functional teams.
Position Requirements
10+ Years work experience
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