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The Opportunity:

Avantor is looking for a detail-oriented and experienced Quality Engineer to join our team in Gliwice, Poland. In this role, you will take ownership of quality management for qualification and validation activities, playing a key role in our quality assurance function. You will also be responsible for managing Quality Engineering documentation and processes, ensuring strict compliance, and driving continuous improvement.

This is a full-time position based at our key facility in Gliwice, specializing in quality assurance, manufacturing, and logistics to support the pharmaceutical, biotech, and research industries. In addition to a competitive salary, we offer a comprehensive benefits package including a performance-based bonus, MyBenefit card, private medical healthcare, and recognition awards.

Working hours: Monday to Friday, core hours.

The Team

You will be part of a dynamic Quality Assurance Team of 5 associates responsible for qualification and validation processes, as well as the verification of qualification documentation. The site offers a collaborative environment where employees work across teams to deliver high-quality solutions. You’ll also have access to career development opportunities and resources to foster professional growth and innovation.

What we’re looking for

• Fluent English and Polish language skills (minimum B2 level)
• Degree in Chemistry, Chemical Engineering, or a related Engineering field
• Strong background in validation and qualification, including knowledge of statistical data analysis, Good Manufacturing Practices (GMP), and Quality Management Systems (ISO 9001, ISO 13485, 21 CFR 210/211/820/11, GMAP 5)
• Preferred experience in quality assurance, chemical manufacturing, or the pharmaceutical industry
• Proficiency in MS Office and excellent organizational skills with keen attention to detail

How you’ll thrive and make an impact

• Prepare and assist in the development of qualification plans, protocols, risk assessments, and documentation to ensure compliance with relevant standards (ISO 9001, ISO 13485, 21 CFR 210/211/820/11)
• Perform and coordinate qualification testing and systems validation, overseeing the execution of qualification activities to meet requirements and regulatory standards
• Identify opportunities for process improvements, propose and implement necessary changes, and ensure ongoing compliance with Good Manufacturing Practices (GMP)
• Act as a subject matter expert, providing technical and quality support during customer and regulatory inspections, and assisting in quality initiatives, risk assessments, and continuous improvement efforts
• Ensure compliance with established manufacturing processes, identifying and addressing any areas of improvement

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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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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.