Quality Line Reference (Inspection)

We're looking to hire Quality Line Reference Technicians for our Fishers, Indiana site!

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
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance

Schedule:

• 8 hour shift

Experience:

• performing quality control test: 3 years (Required)
• healthcare environment (medical device or phrama): 3 years (Required)
• visually inspected products: 3 years (Required)
• Quality inspection: 3 years (Required)

Work Location: In person