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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 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
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