Business Process Expert
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices and Pharmaceutical organization, based in Noord-Brabant Netherlands.
Very large Medical Devices company who is currently merging +- 100 QMS into one global operating QMS.
ROLE DESCRIPTION
Works, as an expert on quality business processes, on the development of medium term policy for his business process, resulting into a vision/roadmap.
Distinctive is a high degree of original, out of the box thinking, needed to find solutions to the assignments.
Formulates new solutions by integral, original thinking and adds new concepts/elements to his sub discipline.
Combines abstract ideas at a high conceptual level, and generates new types of solutions. Formulates, as a recognized authority, solutions across multiple disciplines to effectively achieve goals together.
Builds actively networks with key contacts in- and outside Philips for his specialism to keep abreast of new developments/insights. May lead multi-disciplinary change projects, managing a significant number of people.
Typically requires a Master’s degree with > 5 years of related experience in business processing.
RESPONSIBILITIES
As part of the End to End (E2E) Q&R/ QMS team, your main role is to provide support to E2E Programs and Projects as assigned in support of direct supervisor.
Key areas of responsibilities within your role are the following:
• Participate directly as the Quality Management System Expert in E2E deployment programs, in the Idea 2 Market, Market 2 Order, Order 2 Cash and applicable Enabling process arenas.
• Ensuring compliance requirements and controls are embedded in applicable processes.
• Support setup and deployment of the Quality Management Systems along business model lines as identified by End to End teams.
• Create a solid network with E2E Program and Project teams, ARIS process modeling teams, Business Management System and Quality Management System owners, as well as any other stakeholders to support objectives.
REQUIREMENTS
Quality and Regulatory Specialist with at least 5+ year experience in Medical Devices at a high level.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.
