More jobs:
Analyst, Quality
Job in
Saint Paul, Ramsey County, Minnesota, 55112, USA
Listed on 2026-06-18
Listing for:
TechLink+
Full Time
position Listed on 2026-06-18
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst, QA Specialist / Manager
Job Description & How to Apply Below
Analyst, Quality
Location (On-site, Remote, or Hybrid?):
Saint Paul, MN (onsite)
Contract Duration:
Contract until 01/22/2027
Working hours:
8:00am - 5:00am
Total hours: 40
Essential Functions
- Ensure Regulatory Compliance records are accurate, complete, and maintained in accordance with applicable requirements.
- Prepare, review, and maintain quality system and regulatory compliance documentation and records.
- Maintain and update compliance related database records.
- Support QMS document control processes.
- Assist with the creation, maintenance, and updating of training materials and training audiences.
- Identify discrepancies between metadata fields and approval records.
- Update required fields in Windchill to ensure alignment with approval records.
- Learn and effectively navigate electronic systems used to manage records and data.
- Demonstrate initiative to ensure work is completed accurately and thoroughly.
- Maintain organized, detail-oriented work practices.
- Assist in the development and execution of streamlined business systems to effectively identify and resolve quality issues.
- Apply sound, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues.
- Support company initiatives as directed by management and in alignment with the Quality Management System (QMS).
- Comply with U.S. Food and Drug Administration (FDA) regulations, other applicable regulatory requirements, company policies, operating procedures, processes, and task assignments.
- Maintain positive, professional communication and collaboration with employees, customers, contractors, and vendors at all levels.
- Perform other related duties and responsibilities as assigned.
- 2-5 years of quality and/or regulatory experience, or
- 2 years of relevant industrial experience, typically within quality, product development/support, or scientific affairs functions.
- Working knowledge of regulations and standards affecting medical devices.
- Strong attention to detail and organizational skills.
- Ability to learn new systems and processes efficiently.
- Bachelor's degree preferred in Biotechnology, Biology, Chemistry, Engineering, or a related scientific discipline.
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