Quality Inspector

Saltera Group; Chaska (MN); On-site; USD 40,000 - 60,000; Full time

Job summary

A medical device manufacturing organization in Chaska, MN, seeks a Quality Inspector to ensure product safety and compliance. Key responsibilities include performing detailed inspections, maintaining accurate records, and collaborating with teams to improve processes. Ideal candidates have experience in cleanroom environments and a strong understanding of FDA and ISO standards. This hands-on role emphasizes meticulous attention to detail and adherence to quality protocols.

Qualifications

• Experience in medical device or pharmaceutical manufacturing is preferred.
• Familiarity with cleanroom work, quality inspection, and process documentation.
• Understanding of FDA, ISO 13485, and GMP compliance standards.

Responsibilities

• Perform visual and dimensional inspections during production.
• Operate production equipment to maintain accuracy and output.
• Follow GMP, FDA, and ISO standards.

Skills

Attention to detail

Strong communication skills

Mechanical aptitude

Basic proficiency in Microsoft Office

Tools

Microscopes

Calipers

Micrometers

Gauges

Job description

Saltera HR is proud to partner with a medical device manufacturing organization operating in a clean, high-precision environment where quality is non‑negotiable. The Quality Inspector plays an essential role in ensuring that every product leaving the facility is safe, compliant, and built to the exact standards required for patient use.

This role is hands‑on and detail focused. It is a strong fit for someone who takes pride in careful work, consistency, and doing things right the first time.

What You Will Do

Inspection and Quality Control

• Perform visual and dimensional inspections during and after production
• Use microscopes, calipers, micrometers, gauges, and precision measurement tools
• Identify and document non‑conformances and assist in root cause and corrective action processes
• Maintain accurate inspection logs and production records

Manufacturing Support

• Operate and monitor production equipment to maintain accuracy and output
• Package, label, and prepare finished products to meet regulatory requirements
• Partner with Production, Quality, and Engineering on continuous improvement efforts

Compliance and Safety

• Follow GMP, CGMP, FDA, ISO 9001/13485, and internal SOPs
• Maintain cleanroom standards, including proper gowning and contamination control
• Promote and practice safe work habits at all times

What You Bring

• Experience in medical device or pharmaceutical manufacturing preferred
• Hands‑on familiarity with cleanroom work, quality inspection, and process documentation
• Working understanding of FDA, ISO 13485, and GMP compliance standards
• High attention to detail, strong communication skills, and comfort following defined procedures
• Mechanical aptitude and comfort learning equipment and inspection tools
• Basic proficiency in Microsoft Office and data entry systems

What Success Looks Like

• Accurate, timely inspections and documentation that maintain regulatory compliance
• Consistent product quality with reduced non‑conformance occurrences
• Smooth communication between production and quality teams
• Active contribution to process and product improvements

Work Environment

• Cleanroom setting with gowning requirements and strict hygiene standards
• Standing and performing hands‑on work for extended periods
• Use of microscopes and small precision instruments
• Climate‑controlled, structured production environment

EEO Statement

Saltera HR is proud to partner with organizations who value people. We support workplaces grounded in respect, safety, and equal opportunity. All qualified applicants will be considered.