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Quality Technician

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SGH Medical Pharma

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Location:
France , Val-Revermont

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Contract Type:
Employment contract

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Salary:

Not provided

Job Description:

The SGH Medical Pharma group is a European leader in medical devices and drug delivery solutions. Building on recent major developments in the field of in vitro diagnostics and as a beneficiary of the “industry modernization” recovery plan, our group continues to grow and strengthen its structure. The SGH Medical Pharma group now offers a comprehensive range of services, from standard production to specific development and medical subcontracting. In addition to multi-site manufacturing certified to ISO 13485/15378/14001, including ISO 8 clean rooms, we offer our customers the full benefit of our expertise in quality, R&D, industrialization, and marketing.

Job Responsibility:

  • ensure the compliance and quality of manufactured, received, and shipped products
  • participate in and contribute to improving the performance of the quality department
  • perform and record incoming product inspections in accordance with inspection documents
  • perform visual and appearance inspections
  • perform metrological inspections using the company’s measuring equipment (caliper, scale, measuring column, shims, inspection gauges, leak test)
  • perform sampling inspections (using statistical tables)
  • perform production data checks (work orders/components/materials/dyes/adjustment tolerances)
  • validate the conformity of products and documentation received (components, materials, subcontracting)
  • participate in drafting acceptance inspection ranges
  • participate in repackaging cartons damaged during transport
  • check batch files and release batches of finished products (review batch files, release batches under the ERP)
  • ensure compliance with Good Manufacturing Practices (GMP) and raise awareness among operators
  • handle complaints related to subcontracting
  • conduct field and subcontractor audits
  • promote quality among the logistics and procurement teams (guide teams towards problem solving and the implementation of corrective actions following internal non-conformities)
  • monitor acceptance indicators
  • carry out various tasks for the quality department as required
  • act as backup for quality coordinators as required

Requirements:

  • two-year degree in quality or equivalent
  • proven initial experience in an industrial environment, ideally in the medical device sector
  • familiar with good manufacturing practices (GMP)
  • knowledge of the ISO13485 standard is a plus
  • good team player
  • rigor
  • organizational skills
  • dynamism
  • autonomy
  • proactive
  • know how to take initiative to contribute to the continuous improvement of quality processes

Nice to have:

knowledge of the ISO13485 standard

What we offer:
  • permanent position
  • attractive compensation
  • meal vouchers
  • RTT (reduced working hours)
  • share in the company’s profits
  • health insurance
  • life insurance
  • training in our business and our products

Additional Information:

Job Posted:
December 12, 2025

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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