Avantor is looking for a meticulous and committed Quality Engineer to join our Quality Projects team at our key site in Gliwice. If you have experience in process validation, quality documentation, and want to make a real impact on product quality in the pharmaceutical, biotech, and research industries – this role is for you!
Prepare and execute validation documentation (process and cleaning).
Develop risk analyses such as Cause & Effect Matrix and FMEA.
Define Critical Process Parameters (CPP) and Critical Quality Attributes (CQA).
Train operational teams involved in validation activities.
Review manufacturing and testing records for completed lots.
Analyze deviations, CAPAs, and documentation amendments.
Prepare validation summary reports.
Review and approve external qualification documentation.
Act as a subject matter expert during customer audits and regulatory inspections.
Create and update SOPs and work instructions.
Support quality initiatives, investigations, and risk assessments.
Ensure compliance with GMP and quality systems (e.g., EtQ, Impuls EVO).
University degree in engineering, chemistry, biotechnology, or a related technical field.
Fluent in Polish and English (minimum B2 level).
Validation experience and knowledge of quality management systems are a plus.
Familiarity with ISO 9001, ISO 13485, and GMP principles.
Strong proficiency in MS Office.
Excellent attention to detail and organizational skills.
Ability to work independently and collaboratively.
Analytical thinking and problem-solving skills.
Full-time employment on a single shift schedule (Monday to Friday).
Competitive salary and performance-based bonus.
Benefits package including MyBenefit card, private medical care, and employee recognition programs.
Opportunities for career development and participation in innovative projects.
A collaborative team environment focused on quality improvement and product excellence.
Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.
Why Avantor?
Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.
The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.
We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!
EEO Statement:
We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.
If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
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