Quality Line Reference (Inspection)

Responsibilities:

Perform in-process, visual, dimensional, functional, and packaging controls according to the control plan of the manufactured product

Be the reference key-person for product quality within the shift with reference to the production lines to which they are dedicated

Cooperate with the QC laboratory for the evaluation of the defects

Monitor production lines status in coordination with the other functions, recording the control results and the other required information,

Guarantee a high level of cleaning and tidiness of the work areas

Initiate deviations and OOS and participate in the investigations and solving activities for the non-conformities that occur during the shift

Support personnel training activities

Qualifications:

Basic computer application knowledge

Prior experience in manufacturing or quality control

Knowledge of device manufacturing/pharma Quality Management System processes and features

Experience in healthcare device/pharma manufacturing environment.

International travel may be required, based on business needs

Ability to work weekends

Stevanato Group is an Equal Employment Opportunity (EEO) employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.

Job Type: Full-time

Benefits:

401(k)

401(k) matching