Quality Associate

Working at Freudenberg: We will wow your world

Responsibilities:

• Review manufacturing documentation and analysis results of raw materials and products

• Release or block materials and products according to applicable specifications, following consultation

• Prepare test certificates and other quality documents

• Manage, archive, and properly file documents, records, and retention samples

• Prepare shipments from the Quality Assurance department (e.g., accompanying documentation)

• Assist in handling deviations in collaboration with other departments

• Contribute to the collection and evaluation of quality metrics (e.g., QRK)

• Participate in the creation and revision of work instructions (SOPs)

Qualifications:

• Completed vocational training, e.g., as a chemical laboratory technician, CTA, office management clerk, or a comparable qualification

• Interest in quality-related processes and accuracy in documentation

• Initial professional experience in quality assurance or a regulated environment, e.g., in a laboratory

• Structured and conscientious work style with enjoyment of responsible routine tasks

• Basic knowledge of working with IT systems, databases, and common office applications

• Strong team spirit, sense of responsibility, and commitment to the quality of components and products

• Excellent German language skills and basic English skills, both written and spoken

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Hemoteq AG