Quality technician

Today, the SGH Medical Pharma Group offers a complete range of services, from standard production to specific development and medical subcontracting. In addition to ISO 13485/15378/14001-certified multi-site manufacturing, part of which takes place in an ISO 8 cleanroom, we provide our customers with all our expertise in quality, R&D, industrialization and marketing. To find out more: https://www.sgh-medical.com

Would you like to join: An innovative, ambitious group on a human scale, with a project full of passion and meaning, working as part of an expert team with a wealth of personalities? We have a great opportunity for you to join our team as a Quality Technician based in Val-Revermont (01).

We offer

• A permanent position
• Attractive remuneration
• Meal vouchers
• Reduced working hours
• Company profit-sharing scheme
• Mutual insurance & provident scheme
• Training in our professions and products

As a Quality Technician, you will report to the site Quality Manager. Your main mission will be to guarantee the conformity and quality of products manufactured, received and dispatched. You will participate in and contribute to improving the performance of the quality department.

In this capacity, your main tasks will be as follows:

• Carry out and record incoming product checks in accordance with inspection documents
• Carry out visual and appearance checks
• Carry out metrological inspections using the company’s measuring equipment (calipers, scales, measuring columns, shims, inspection templates, leak tests)
• Carry out sampling checks (use of statistical tables)
• Carry out production data checks (OF/components/material/color/tolerance settings)
• Validate conformity of products and documentation received (components, materials, subcontracting)
• Participate in drafting incoming inspection procedures
• Release finished product batches (batch file review, batch release in ERP).
• Ensure compliance with Good Manufacturing Practices (GMP) and raise operators’ awareness
• Handle complaints related to subcontracting
• Carry out field audits
• Coordinate and monitor safety and environmental indicators
• Manage and monitor waste: certification of service providers

Profile required

• You have a 2-year higher education qualification in quality or equivalent, and initial successful experience in an industrial environment, ideally in the medical devices sector
• You are familiar with Good Manufacturing Practices (GMP), and knowledge of ISO13485 is a plus
• A good team player, you are also recognized for your rigor, organizational skills and autonomy
• A self-starter, you are able to take the initiative and contribute to the continuous improvement of quality processes

Do you meet all these criteria? Then you’re the ideal candidate!

You don’t meet all these criteria? Try your luck by applying – we’ll take a close look at your application!

We are proud to promote diversity and equal opportunity within our teams. We believe that our differences make the difference, and that an inclusive working environment will stimulate our growth as a company, as teams and as individuals. We will therefore consider all applications*, promoting an inclusive work culture where everyone can feel they belong. All applications will be considered regardless of origin, background, religion, gender, sexual orientation, gender identity, disability…