Quality Technician – Line & Packaging

STERIS - Operations

Plymouth, MN

JOB DETAILS
SKILLS
Acceptance Testing, Administrative Skills, Calibration, Code of Federal Regulations, Computer Skills, Continuous Improvement, Corrective Action, Desktop PC, Documentation, ERP (Enterprise Resource Planning), Environmental Monitoring, FDA (Food and Drug Administration), FDA Requirements, GMP (Good Manufacturing Practices), Healthcare, High School Diploma, ISO (International Organization for Standardization), ISO 9001, Lean Manufacturing, Manufacturing, Manufacturing Operations, Mechanical Testing, Microsoft Excel, Microsoft Word, Problem Solving Skills, Process Improvement, Product Documentation, Product Management, Product Testing, Project Tracking, Quality Control, Regulations, SAP, Team Player, Time Management, Typing
LOCATION
Plymouth, MN
POSTED
2 days ago

The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards.

Position Summary:

The Quality Technician supports manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes.

HOURS: 5am - 1:30pm Monday through Friday & overtime as business needs

*Training may require 6/7/8am start times as needed

LOCATION: 14905 28th Ave North Plymouth, MN

PAY: $22.47 - $27.76 (paid bi-weekly) & bonus participation

What You'll Do:

  • Assists in production line Quality investigations and associated problem-solving activities.
  • May coordinate and conduct in-process and final QC product acceptance testing, depending on facility.
  • Investigates production line stoppages to identify corrective actions.
  • Identifies and documents product and process non-conformances.
  • Participates on a Material Review Board to review and process non conformance reports.
  • Reviews DHR’s and supports batch record release.
  • Enters and retrieves Quality data from local and global systems.
  • Performs site calibration activities and recordkeeping.
  • Executes environmental monitoring processes and recordkeeping.
  • Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release.
  • Complete other duties as assigned.

**Skills, Abilities, and Experience: **

Required:

  • Minimum of three (3) years of experience in a manufacturing or repair environment or other technical production tasks AND a high school diploma or equivalent.- Minimum of one (1) year of experience in a manufacturing or repair environment or other technical production tasks AND an associate degree.

  • PC experience and familiarity of common desktop applications including Excel and Word.

  • Ability to:- work in a fast-paced environment with strict deadlines

    • generate detailed, high-quality documentation.

    • work with others in analyzing and solving technical problems.

    • collaborate with others.

    • work in a professional manner to support team actions.

    • effectively manage work tasks.

Preferred:

  • Previous experience working as a Quality Technician in a regulated, chemical manufacturing industry.

  • Experience working in systems like Trackwise, SAP, and Propel to manage products and track work instructions.

  • Continuous improvement or process improvement experience in a work setting.

  • Expereince working with Lean Manufacturing principles.

  • ISO/FDA audit experience.

Other:

  • Lifting, pushing, and/or pulling 25-50lbs.
  • Bending, walking, standing, sitting, typing, hand manipulation, and/or visual acuity may be required in this role.
  • Safety sensitive position.

What STERIS Offers:

We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future.

Here is just a brief overview of what we offer:

  • Market Competitive Pay
  • Extensive Paid Time Off and (9) added holidays
  • Excellent Healthcare, Dental and Vision Benefits
  • Long/Short Term disability coverage
  • 401(k) with company match
  • Maternity & Paternal Leave
  • Additional add-on benefits/discounts for programs such as Pet Insurance
  • Tuition Reimbursement and continued educations programs
  • Excellent opportunities for advancement and stable long-term career

You should be proficient in:

  • ISO 13485
  • Manufacturing Instruction (MI)
  • FDA Regulations
  • Mechanical Testing
  • Lean Manufacturing Principles
  • ISO 9001 Certification Experience
  • Good Manufacturing Practices (GMP)
  • Experience in a Manufacturing Environment

Machines & technologies you'll use:

  • ERP Software
  • Quality Control Software

About the Company

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STERIS - Operations