Stryker

Senior Quality Management Systems (QMS) Specialist

Poland · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

EmployerStryker
LocationPoland
Work styleWork style not stated
Employment typeFull time
Employer posted17 Sep 2026

Work Flexibility: Not available

Join a team that helps ensure the highest quality standards across a global medical technology organization. In this role, you will contribute to the development, maintenance, and continuous improvement of quality management systems that support regulatory compliance, operational excellence, and business growth. Your work will directly support patient safety, product quality, and organizational success.

What You Will Do

Ensure compliance of the Quality Management System (QMS) with applicable global regulatory requirements, including FDA, ISO standards, EU Medical Device regulations, and country-specific requirements.
Develop, implement, and continuously improve local and regional quality management system processes aligned with global quality standards and business needs.
Serve as a local process owner for assigned quality system processes, ensuring effectiveness, compliance, and ongoing process improvement.
Coordinate management reviews and quality planning reviews, including preparation of metrics, trend analysis, and follow-up actions.
Support internal and external audits by coordinating activities, maintaining documentation, and driving timely resolution of findings.
Implement and maintain QMS training programs to ensure employee compliance with quality requirements and procedures.
Develop, maintain, and update quality policies, procedures, and controlled documentation to support business operations.
Lead or support projects to enhance quality system effectiveness, assess regulatory requirements, implement best practices, and drive continuous improvement initiatives.

Show full description

What You Will Need

Required Qualifications

Bachelor’s degree or equivalent
Minimum 2 years of experience in a Quality Assurance, Quality Systems, or Regulatory Affairs role within regulated environment
Knowledge of medical device quality and regulatory requirements, including ISO 13485 and applicable global regulations.
Fluent English (minimum B2 level), both written and spoken.
Experience supporting quality system processes such as audits, management reviews, document control, or quality planning.
Proficiency with standard business software and computer applications.
Strong communication skills.

Preferred Qualifications

Experience working within the medical device industry.
Knowledge of Medical Device Single Audit Program (MDSAP) requirements and U.S. FDA Quality System Regulations (21 CFR Part 820).
Experience participating in or leading quality system improvement projects.

Please note it is a 24-month fixed term contract

Poland Pay Ranges:

Poland, Skawina: zł107.100 - zł178.600 PLN Annual
Poland: zł123.200 - zł205.400 PLN Annual

At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker’s comprehensive benefits package.

If you’d like to learn more about the salary or the benefits associated with this role, your recruiter will be happy to walk you through the details as you progress through the hiring process.

Travel Percentage: None

See how well you match this job Apply on the employer’s site ↗

Check your resume against this job Free, no sign-up. Nothing you paste is stored.

Staying safe while you apply

Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
Prepare honestly.
Build interview stories and application drafts from your own evidence.
Keep track.
Save the role and record your own application status and follow-ups.

Create a free workspace or log in.