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Role Summary

Experience in the following areas preferred

quality management/quality engineering in the in vitro diagnostics industry or its suppliers

production-related positions in the in vitro diagnostics industry - such as production managers, quality control managers or research and development positions responsible for design or validation

Experience in quality management in laboratories, hospitals and other IVD testing centers

academic research or commercial research and development, in a quality-controlled environment, involving technologies relevant to IVD (e.g. ELISA, PCR, flow cytometry, cell staining, cell microscopy)

Requirements

• a diploma of completion of higher education or technical studies in an appropriate field. Relevant subjects include: medicine, pharmacology, biomedical engineering or bioengineering, microbiology, biotechnology, biochemistry, medical technology, mechanical engineering, electronic engineering
• at least four years of professional experience in health care, of which at least two years in quality management. (At least some of this experience is expected to be related to in vitro diagnostic medical devices)
• knowledge of English enabling the free performance of duties (min. B2)
• valid driving license necessary to perform your job
• readiness to undertake frequent business trips

Benefits

• full-time employment (employment contract) in the structure of a stable, international company that is a leader on the global market
• the work takes place in the field, so you can do it while living anywhere in Poland
• necessary work tools (including a company car for private use)
• attractive employment conditions (extensive social package with a choice of benefits, private medical care, sports card, life insurance, online foreign language courses, employee recommendation program)
• full training and the opportunity to improve professional qualifications

friendly working atmosphere

Acting pursuant to Art. 24 section 1 of the Act of June 14, 2024 on the protection of whistleblowers (Journal of Laws of 2024, item 928), we would like to inform you that in SGS Polska Sp. z o. o. and in SGS Global Business Services Europe Sp. z o. o. The internal reporting procedure applies.

The internal reporting procedure is available on the website at the link below:

Internal reporting procedure | SGS Poland

About the Company

SGS is a global leader in testing, inspection and certification. We operate a network of over 2,500 laboratories and offices in 115 countries, supported by a team of 99,500 dedicated professionals. We have over 145 years of experience in providing excellent services - we combine the accuracy and precision that characterize Swiss companies to help organizations achieve the highest standards of quality, compliance and sustainability.

Our slogan - when you need to be sure - is a promise emphasizing our commitment to trust, reliability and reliability that enable companies to develop with confidence. We proudly deliver our expert services as SGS, supported by our other trusted and highly specialized brands such as Brightsight, Bluesign, Maine Pointe and Nutrasource.

SGS is a company listed on the Swiss Stock Exchange under the symbol SGSN (ISIN CH0002497458, Reuters SGSN.S, Bloomberg SGSN:SW).

Description of the job offer

Conducting audits in enterprises in the scope of Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and preparing post-audit documentation in English.