Quality Manager

The SGH Medical Pharma group now offers a complete range of services, from standard production to specific development, including medical subcontracting. In addition to ISO 13485/15378/14001-certified multi-site manufacturing, part of which is in an ISO 8 cleanroom, we offer our customers all our expertise in quality, R&D, industrialisation 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 passionate and meaningful project, 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 manager based in Val-Revermont (01).

We offer 

• A permanent position
• Attractive remuneration
• Meal vouchers
• Reduced working hours
• A share in the company’s profits
• Mutual insurance and provident fund
• Training on our business and products

Reporting to the Site Quality Manager, you will ensure product conformity and promote quality within the production teams.

As such, your main tasks will be:

Quality in production

• Carrying out product checks at the workstations according to the control documents
  • Appearance checks
  • Sampling checks: use of statistical tables
  • Checking production records (including traceability)
  • Metrological checks using the company’s measuring equipment (calipers, scales, measuring columns, shims, inspection templates)
• Checking that the checking and recording operations carried out by the operators and technicians run smoothly
• Taking part in the integration of new production employees
• Organise sorting operations
• Participate in the re-reading of production control areas
• Operational management of non-conformities: carton feedback, recording, follow-up and closure

Quality

• Training and communication of good practices to operators in terms of: quality, good manufacturing practices, safety, hygiene, cleanliness, environment (application of control ranges and compliance with good frequencies, work instructions, OF monitoring records, etc.)
• Ensure that hygiene, cleanliness and tidiness are maintained at the work stations
• Check batch records and release batches produced
• Alert his/her supervisor in case of difficulties
• Leading the production team to solve problems and implement corrective actions following internal nonconformities

Additional tasks

• Assist the Quality Coordinators assigned to the team
• Perform various tasks for the quality department as required
• Assist with new projects

Required profile

• You have at least 1 year of successful experience in a quality team in an industrial environment
• You are familiar with the Office package and control tools
• You are familiar with Good Manufacturing Practices
• Knowledge of ISO 13485 is an advantage
• You have good organisational and teaching skills
• You are a team player with good interpersonal skills and are recognised for your thoroughness and ability to work well with others
• You are flexible enough to work occasional shifts according to the needs of the department.

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

Don’t meet all these criteria? Take a chance and apply – we’ll look at your application!

We pride ourselves on promoting diversity and equal opportunities within our teams. We believe that our differences make a difference and that an inclusive working environment helps us grow as a company, as teams and as individuals. We will therefore consider all applications* and promote an inclusive working culture where everyone can feel they belong.

All applications will be considered regardless of origin, background, religion, gender, sexual orientation, gender identity, disability…