Espagnol à France

With 1,500 employees and 14 production sites across 3 continents, STERIMED is the world’s leading manufacturer of materials and packaging systems for the sterilization of medical devices. Sterimed develops, produces, converts, and markets various solutions such as bacterial barrier substrates and preformed sterilization packaging, both for hospitals and medical device manufacturers.

Sterimed is characterized by a strong entrepreneurial DNA and has been experiencing sustained growth, both organically and through acquisitions. Since its founding in 2016, the size of the group has multiplied by 4.5 and 10 acquisitions have been completed since 2017.

As part of the strategic SAP deployment project across the group, Sterimed is recruiting a Business Process Owner – Quality (M/F) to join the Group Innovation & Compliance Director.

Based at the group’s headquarters in Boulogne-Billancourt, you will work not only within the SAP project team but also with the Quality Managers of each site and the Group Continuous Improvement team. By collecting information and building databases (inspection plans, release data, traceability, etc.), you will facilitate access to information and help share expertise.

Your daily missions will include:

• Gather current quality process practices and promote them across all sites
• Understand and master SAP best practices as defined in the core model and deployed at the pilot site, to support deployment at subsequent sites (experience with the QM module is a plus)
• Define and standardize quality processes and key performance indicators with the SAP standard model
• Ensure local Key Users deploy these processes on each site
• Identify organizational impacts and anticipate change management actions with the change management team during each deployment, to support adoption
• Train users on new SAP processes and solutions
• Update training documentation and test scenarios
• Have the solution validated by domain Key Users from each site after testing
• Follow up on post-go-live change requests to maintain solution consistency and integrity, and suggest evolutions meeting group standards

• Degree from an engineering school or equivalent university education (BAC+4/5) in methods or quality
• Minimum of 5 years of operational quality experience in manufacturing/processing industries
• Proven experience in implementing a Quality Management System, ideally in highly regulated environments such as ISO 13485 or pharmaceutical standards
• Experience in project management
• Team player with a proactive mindset
• Strong process orientation and organizational skills
• Ability to make decisions on business processes aligned with Sterimed’s strategic goals
• Strategic thinking: harmonization and simplification across the group
• Strong communication and influencing skills with cross-functional teams
• Ability to report project progress to stakeholders (logistics, production…)
• Experience with SAP
• Fluent in English – Spanish is a plus

• Proudly certified Great Place to Work
• Remote work available
• 27 days of paid vacation
• RTT (Reduction of Working Time) / Executive status (218 workdays/year) / Time Savings Account agreement

Sterimed is committed to creating an inclusive and accessible work environment. Please don’t hesitate to inform us of any accommodations needed to support your participation in the recruitment process.

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