Quality Systems Specialist — Medical Devices & Compliance

Straumann Group; Wrocław; On-site; PLN 80,000 - 130,000; Full time

Job summary

Straumann Group is seeking a Quality Assurance role in Wroclaw, Poland, to maintain the Quality Management System and ensure compliance with regulatory standards. The role covers procedures, records, audits, and cross-functional collaboration to support medical device manufacturing.

The candidate should bring robust experience in quality systems, internal and supplier audits, and proficiency with standard quality tools, aiming to uphold safety and compliance across site operations.

Qualifications

• 2+ years’ quality experience in medical device manufacturing.
• 2+ years’ experience in internal and supplier audits.
• 2+ years’ experience producing formal procedures and work instructions.
• 2+ years’ experience using basic quality tools (RCA, Fishbone, SPCs, checklists, histograms, Pareto, scatter diagrams).
• Proficient with Microsoft Office.

Skills

Quality experience

Audits

Procedures

Quality tools

Documentation

MS Office

Education

Associate degree

Tools

RCA

Fishbone

SPC

Checklists

Histograms

Pareto

Scatter plots

Process mapping

Flow charts

Job description

Straumann Group is seeking a Quality Assurance role in Wroclaw, Poland, to maintain the Quality Management System and ensure compliance with regulatory standards. The role covers procedures, records, audits, and cross-functional collaboration to support medical device manufacturing.

The candidate should bring robust experience in quality systems, internal and supplier audits, and proficiency with standard quality tools, aiming to uphold safety and compliance across site operations.