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## **The Opportunity:**## Managing on-site quality and validation activities.### **Key Responsibilities:*** 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).### **Requirements:*** 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.### **We Offer:*** 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.**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 peoples 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 moms 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.**Privacy Policy:**We will use the personal information that you have submitted to us in order to consider your application for the relevant role.Your privacy is important to us. Please for our Privacy Policy which explains the purposes for which we will use your personal information and the ways in which we will handle and retain your information. It also explains the rights you have in relation to your information, and how to contact us with any queries or requests.**3rd Party Non-Solicitation Policy:**By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.**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!Avantor, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries. Our portfolio is used in virtually every stage of the most important research, development and production activities in the industries we serve. One of our greatest strengths comes from having a global infrastructure that is strategically located to support the needs of our customers. Our global footprint enables us to serve more than 225,000 customer locations and gives us extensive access to research laboratories and scientists in more than 180 countries. We set science in motion to create a better world.
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