Quality Technitian

vwr; Gliwice; On-site; PLN 42,000 - 65,000; Full time

Benefits offered by this job

Private healthcare

Sport card

Social fund

Food vouchers

Free beverages

Professional development

Job summary

Avantor is seeking a dedicated Quality Technician to join our Quality team in Gliwice, Poland. This full-time role supports quality systems, documentation, and continuous improvement in a regulated environment.

You will work with cross-functional teams, contribute to audits, maintain QA records, and help ensure compliance with GMP and ISO standards. English proficiency is required; Polish is an advantage.

Qualifications

• Bachelor's degree in a scientific/technical field or equivalent experience.
• Professional working proficiency in English; Polish preferred.
• Experience in QA/QC, manufacturing, or regulated environments (medical device/pharma).
• Knowledge of quality systems, documentation control, GMP and ISO standards is a plus.
• MS Office experience (Word, Excel, Outlook, PowerPoint).
• Strong attention to detail, organizational and communication skills.

Responsibilities

• Provide information, support, and guidance to teams within the quality function.
• Assist with training and cross-training activities.
• Support generation, maintenance, update and distribution of quality documentation and QA forms.
• Perform electronic data entry and maintain quality records per procedures.
• Participate in process improvement initiatives and support quality procedures/policies.
• Contribute to ISO 9001, ISO 13485 and GMP audits and related documentation.

Skills

Quality Assurance

Quality Control

GMP/ISO

Documentation

Attention to detail

Communication skills

English proficiency

Education

Bachelor's degree in science/tech

Tools

Microsoft Office

Job description

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

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.

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 [e-mail] 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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