Johnson & Johnson Carrières

QC Inspector

Le Locle, Neuchâtel
Quality Control

Description du poste

Requisition ID: 1805651692W

Caring for the world, one person at the time, has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science – bringing innovative ideas, products and services to advance the health and well-being of people.

Johnson & Johnson is one of the leading health care companies in the world, with over 6,000 people working for Johnson & Johnson companies in Switzerland. Johnson & Johnson’s footprint covers sites and companies across three of its sectors -  Consumer Health CareMedical Devices and Pharmaceuticals businesses, situated in a number of locations across Switzerland.

Our site in Le Locle is looking for a:
QC Inspector - 80%

• Inspect (dimensional & visual) the implants, the components and the raw materials according to the specifications to ensure conformity of products

• Perform documentation review according to good documentation practices

• Perform final release batch according to the requirements to ensure conformity.

• Perform final testing according to the certification of production operators

• Initiate non-conformances according to specified requirements

• Verify that results of rework are completed according to specified requirements

• Treat nonconformities including bounding, identification and quarantining of product

• Raise awareness by explaining and ensuring good documentation and manufacturing practices

• Participate to validations of product or equipment (participation to the definition of inspections methods, inspections of FAI…)

• Archive the DHR (Device History Records) according to specified requirements

• Perform different QC audits in the shop floor.

• Mechanical CFC or equivalent

• Experience in quality control, preferably in the medical industry

• Excellent ability to read and interpret technical drawings and the GD&T and comfortable with control equipment: gauges, micrometers, comparators, profile projector, gauges and CMM (3D measuring device used)

• Knowledge of QA and Regulations in the Medical Device Industry

• Knowledge of software tools such as, Microsoft Word, Excel, PowerPoint, Office

• Strong communication skills, teamwork

• Establish a good collaboration with other departments: production, engineering, planning, procurement and logistics, etc.

• Prioritize effectively to maintain a control of daily activities

• Demonstrated knowledge and application of QSR, MDD, ISO 9001, ISO 13485 and other international standards

• Flexible approach to fluctuating work demand

If this role sounds appealing to you or you know someone who might be interested, please do not hesitate to send us your/their CV!

Emplacement principal
Suisse-Neuchâtel-Le Locle
Medos Sarl (8575)
Quality Control
Requisition ID