QA Supervisor, Medical Devices & Distribution

Johnson & Johnson Co.; Warszawa; On-site; PLN 125,000 - 200,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Bereavement leave

Well-being reimbursement

Insurance plans

Job summary

Johnson & Johnson Vision is seeking a Quality Assurance Supervisor in Warsaw, Poland. You will lead the Quality Inspection team at the Distribution Centre and drive CAPA/NC processes, risk management, and readiness for audits across EMEA.

You should bring 2–5 years of medical device QA experience, leadership capabilities, and fluent English and Polish to ensure robust quality systems and cross‑functional collaboration.

Qualifications

• Bachelor’s degree (or equivalent) in Science or Engineering.
• Medical device experience in a Quality role (2–5 yrs) is preferred.
• English & Polish proficiency required; strong communication skills essential.

Responsibilities

• Lead the Quality Inspection team for the Distribution Centre in Warsaw, Poland.
• Provide Quality support to contact lens distribution operations and third‑party logistics partners.
• Responsible for site CAPA and NC processes and supporting records and metrics.
• Perform risk analyses (FMEA, 5Why) to minimize risk to customers throughout the product lifecycle.
• Lead monthly and quarterly Quality reviews and facilitate decision making.
• Train staff in Quality systems, tools, and objectives; promote continuous improvement.
• Host notified body and internal audits for the distribution centre and related sites.

Skills

Medical device quality

Leadership

Communication (English & Polish)

Interpersonal skills

Self-motivation

Office software

Adobe artwork files

Education

Bachelor's degree in Science or Engineering

Tools

Office applications

Adobe

Job description

Johnson & Johnson Vision is seeking a Quality Assurance Supervisor in Warsaw, Poland. You will lead the Quality Inspection team at the Distribution Centre and drive CAPA/NC processes, risk management, and readiness for audits across EMEA.

You should bring 2–5 years of medical device QA experience, leadership capabilities, and fluent English and Polish to ensure robust quality systems and cross‑functional collaboration.