Sr Supplier Quality Engineer- Services/Channel Partners Illumina

1.0 - 5.0 years

0 Lacs

karnataka

On-site

The work you do every day at Illumina can have a profound impact on the lives of people globally. As part of a team dedicated to expanding access to genomic technology, you will contribute to the realization of health equity for billions of individuals. By enabling life-changing discoveries that improve human health through early disease detection, diagnosis, and innovative treatment options, you will play a crucial role in transforming healthcare for the better. Working at Illumina means being part of a larger mission that goes beyond individual contributions. Regardless of your role, you will have the opportunity to make a difference and grow professionally. Surrounded by exceptional colleagues, visionary leaders, and groundbreaking projects, you will push your boundaries and achieve more than you ever imagined possible. This position is pivotal in overseeing Supplier Quality activities at Illumina, ensuring compliance with Quality System Regulations, company policies, FDA regulations, and ISO standards. By monitoring and enhancing Illumina's product quality and collaborating with suppliers, this role plays a crucial part in achieving operational objectives and driving continuous improvement initiatives. Responsibilities include qualifying, evaluating, and monitoring new suppliers and partners for Illumina products and services. Collaborating with cross-functional teams, you will coach partner processes and contribute to new product development and quality assurance efforts. By driving process and product improvements through supplier development activities and quality investigations, you will play a key role in maintaining high standards. Additionally, you will lead Quality Investigations and CAPA/SCARs to resolve quality issues, conduct supplier audits, and support global initiatives for supplier performance reviews. Your expertise will be crucial in ensuring compliance, driving process standardization, and resolving issues effectively. To excel in this role, you should have experience working with cross-functional teams, strong QMS auditing skills, and proficiency in Quality Management Systems and process engineering methodologies. Experience with non-conformance handling, failure investigation, and risk management activities is essential. Strong communication, negotiation, and project management skills are also required to succeed in this dynamic and fast-paced environment. Travel may be required, both domestically and internationally, to collaborate with teams and partners effectively. While the listed requirements are essential functions of the position, accommodations may be made based on business needs to accommodate additional tasks and responsibilities. In terms of qualifications, a technical discipline background with a Bachelor's, Master's, or PhD degree, along with relevant experience, is necessary. Experience in a regulated environment, particularly in in-vitro diagnostics, is preferred. Practical experience with FDA and ISO regulations, statistical analysis, and electronic product life cycle systems is advantageous for this role.,

Posted 1 week ago

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