Light Tree Ventures Group

About us We are Light Tree Ventures, a company specialized in Research, Development and Manufacturing of LED Light Therapy products for beauty and health. We have offices in the Netherlands, China, the US and India, with our headquarters in Rijswijk. Our team of professionals are the heart of our company and encompass a wide variety of cultures, skills and competences. We love our work and share the ambition to be the best at what we do : create meaningful, well-designed products for LED Light therapy markets worldwide. Light Tree Ventures (LTV) works with brands from all over the world. We develop custom light therapy devices that are being sold online and offline (in Sephora e.g.). This development is often a R&D sprint, designing a prototype and getting it ready for production. A fast and creative process, realizing the next generation product for a brand. LTV also owns several brands for which we develop our own innovative light therapy products. In our India team we are looking for a new firmware developer that create and implement firmware on our LED light therapy devices. You will work together with our team to create new, innovative and exciting light therapy products. So what will you do? Job description We are looking for a Quality Control Engineer. Your main tasks will include: Set detailed guidelines on what needs to be checked and what the quality standards are Update our Quality Management System (QMS) with incidents, fixes and improvements. Audit our systems based on ISO 9001:2015 requirements Determine quality metrics for all manufacturing procedures Monitor the entire production cycle and perform regular tests to identify potential malfunctions as early as possible Inspect product materials(which includes PCB, Components, SMT, etc) and electrical systems for defects and durability Identify the root of technical issues and recommend fixes Prepare reports on malfunctions and corrective actions (e.g. number of defective raw materials per order) Review current blueprints and quality documentation Set and track quality assurance goals (e.g. reduce average turnaround time for quality checks by 20%) Coordinate with external quality assurance auditors and technicians to ensure legal compliance Work with internal teams to increase customer satisfaction by improving the quality of the products Provision of records proving conformity of produced product to specifications. Responsible for product release based on manufacturing and QC records and/or reports. Requirements and skills Bachelor degree in electronic is preferred with 4+ year of Experience. Previous work experience as a Quality Engineer or similar role in any EMS or medical electrical device manufacturing company. Hands-on experience with Quality Management Systems (QMS) and testing methodologies. In-depth understanding of technical documentation Great attention to detail and problem-solving abilities Team spirit, Good analytical skills. Additional certification in Quality Control is a plus. Knowledge of IPC-A-610 for electronics products assembly inspection. Knowledge of ISO13485 preferred. Hands on experience of Risk Management process as per ISO 14971 Good understanding of FDA 21CFR Part 822 / 820 (Good to have) Familiar with tools like Monday.com, Office 365, etc. What we offer: • A highly motivated, young and hardworking team. • Fast growing company with a lot of opportunities to develop yourself. • Awesome products and international clients to work with. • Proper salary, holiday allowance, vacation days. • Your work contributes to the health of the general public. • Opportunities to travel the world.