Description
The selected professional will perform key technical functions within the Quality Department, focusing on the management and maintenance of certification systems, with particular emphasis on ISO standards. They will be responsible for ensuring that all production processes comply with established standards, conducting internal audits, process controls, and finished product verifications to guarantee excellence. This position requires meticulous attention to detail and a commitment to continuous improvement, documenting non-conformities and proposing corrective actions to optimize procedures.
Additionally, the technician will provide substantial support to the Research and Development (R\+D) Department, closely collaborating on innovation projects and new formulations. Their role will be critical in ensuring that new product developments or improvements to existing products align from conception with the highest quality levels required by the market and regulatory requirements. This cross-functional collaboration is essential for integrating quality requirements into the early stages of design and manufacturing, reducing risks and ensuring efficiency.
The role also involves responsibilities related to formulation and manufacturing processes, overseeing that activities are carried out in accordance with technical specifications and good practice protocols. The technician must verify the correct application of operating procedures, handling of raw materials, and control of environmental production conditions where necessary. Their work directly contributes to final product consistency, customer satisfaction, and strengthening the company’s competitive position in the industrial sector.
The position offers a salary exceeding the rates stipulated in the collective agreement for the chemical industry. There is potential for immediate incorporation into the end client’s workforce. The company fosters a professional environment conducive to development and provides a structured career plan for employee growth. Working hours are Monday to Friday, facilitating work-life balance.
Academic training in Chemistry, Pharmacy, or Biological Sciences is required. Proven prior experience working in a Quality Department within an industrial setting is mandatory. Specific knowledge of regulations governing medical devices and cosmetics, as well as hands-on experience in the cosmetics industry, are highly valued. Furthermore, a certified B2 level of English proficiency according to the Common European Framework of Reference for Languages is required.