The Opportunity: Quality Technician Avantor is looking for a dedicated and detail-oriented Quality Technician to join our Quality team. This is an excellent opportunity for someone who enjoys working in a quality-focused environment, supporting quality systems, documentation, and continuous improvement initiatives. This is a full-time position based in Gliwice, Poland . If you have experience in Quality Assurance, Quality Control, GMP or regulated environments and are looking to further develop your career in a global organization, we'd love to hear from you.
What we're looking for Education: Bachelor's degree or equivalent experience in a scientific, technical, or related field Languages: Professional working proficiency in English is required; Polish preferred Experience: Previous experience in Quality Assurance, Quality Control, manufacturing, laboratory, medical device, pharmaceutical, or other regulated environments Knowledge of quality systems, documentation control, GMP and/or ISO standards is considered an advantage Good working knowledge of Microsoft Office applications (Word, Excel, Outlook, PowerPoint) Strong attention to detail, organizational and communication skills How you'll thrive and create an impact Provide information, support, and guidance to teams within the scope of the quality function Assist with training and cross-training activities within the department Support the generation, maintenance, update and distribution of quality documentation and QA forms Perform electronic data entry and maintain quality records in compliance with company procedures Participate in process improvement initiatives and support implementation of quality procedures and policies Contribute to ISO 9001, ISO 13485 and GMP audits and assist with related documentation and compliance activities Support batch review activities and product disposition decisions in accordance with established release procedures Collaborate with cross-functional teams to ensure compliance with quality standards and requirements Provide backup support for department personnel when required Maintain quality and compliance standards within the scope of assigned responsibilities Preferred Qualifications Experience working in a GMP-regulated environment Familiarity with ISO 9001 and/or ISO 13485 standards Experience supporting audits and quality system documentation Why Avantor?
We offer you a multifaceted, full-time role in a dynamic, international environment, participation in the Avantor bonus program, and a comprehensive benefits package, including: Private healthcare Sport card / Benefit cafeteria Social fund benefits Food vouchers for our canteen Free beverages Opportunities for professional development and growth within a global organization #LI-Onsite 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