Senior Quality Engineer

2 Months ago • All levels • Quality Assurance

Job Summary

Job Description

As a Senior Quality Engineer at Illumina, you will play a crucial role in ensuring the quality and compliance of our products. Your responsibilities will include supporting the product lifecycle, reviewing batch records, ensuring the adequacy of manufacturing and quality records, and proactively solving problems. You will also participate in investigations, apply your knowledge of regulations and standards, and monitor Key Performance Indicators (KPIs). This role requires you to work in a fast-paced environment, build relationships with stakeholders, and contribute to the company's mission of expanding access to genomic technology. You'll be part of a supportive environment that encourages skill and knowledge development.
Must have:
  • Experience in a quality assurance regulated environment.
  • Experience with quality management systems including ISO 13485:2016.
  • Strong communication, problem-solving, and organizational skills.
  • Ability to manage and lead change.
  • Excellent attention to detail, well organized and able to work independently and as a team.
Good to have:
  • Experience in an in-vitro medical device environment
  • Good judgment and decision-making skills.

Job Details

What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. Why Us  Illumina are a global leader in genomics –an industry at the intersection of biology and technology. At the most fundamental level, we enable our customers to read and understand genetic variations. We strive to make our solutions increasingly simple, more accessible, and always reliable. As a result, discoveries that were unimaginable even a few years ago are now becoming routine and are making their way into patient treatment. Over the last few years, Illumina has experienced rapid expansion and this Quality Engineer role is supporting our continued growth plans. Why You To be successful as our Quality Engineer you will apply quality regulations and standards and establishing and/or maintaining quality systems. You will have strong analytical, problem solving and organizing skills. You will have excellent attention to detail, be well organized and able to work independently as well as working collaboratively as part of the team. You will thrive in a fast-paced environment and enjoying building relationships with stakeholders within Illumina’s local, regional and global locations. Like you, we know the importance of your role and offer you a collaborative and supportive environment in which you are actively encouraged to continually develop your own skills and knowledge. Responsibilities: * Models Quality culture to the Chesterford site as part of the Manufacturing Operations Quality team. * Provide quality support throughout the product life cycle, including quality control, batch record review and other activities as needed. * Ensures adequacy & completeness of manufacturing and quality records. * Support the development and execution of actions to close gaps in an efficient, technical, and compliant manner. * Proactive approach to structured & practical problem solving. * Participate in investigations to identify problem cause and identification of risks, recommendations, and outcomes * Apply experience and knowledge of regulations and standards (including ISO 13485:2016) to manage risks and guide actions independently * Support the development and ongoing monitoring of Key Performance Indicators from a variety of data sources * Provide management with status updates on assigned responsibilities and goals and escalate issues in a timely fashion. Requirements: * Limited  applied experience in a quality assurance regulated environment necessary. * Some experience working with  quality management systems including ISO 13485:2016 & in-vitro medical device environment preferred * Strong communication, facilitation, planning, problem-solving, and organizational skills appropriate to experience level. * Demonstrated ability or aptitude to learn how to manage and lead change * Analytical, problem solving and organizing skills * Good judgment and decision-making skills; knows how to make trade-off decisions while balancing compliance and business impact preferred. * Flexible, with ability to work effectively in a fast-paced, dynamic environment with shifting and competing demands * Excellent attention to detail, well organized and able to work independently and as a team. Preferred Background  * Typically requires a Bachelor’s degree; or equivalent work experience * You are fluent in English; What can you expect? With Illumina, you can expect a highly competitive salary accompanied by a market-leading benefits package.  You will be part of the global leader in the Sequencing industry where you will find robust growth opportunities and career development within Illumina.  Our team members are bright, energetic, and dedicated—they are the driving force behind our innovation and impact. To attract the best and brightest, we offer a competitive employee benefits program. We view it as a smart investment in our people, one that recognizes the tremendous value they bring to our business every day. At Illumina, we push boundaries. We think beyond the conventional. We dream big. With the energy of so many bright and accomplished people, the opportunities are endless. INDEUR  #LI-EMEA #LI-EUROPE #LI-HYBRID Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.

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About The Company

At Illumina, our goal is to apply innovative technologies and revolutionary assays to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. These studies will help make the realization of personalized medicine possible. With such rapid advances in technology taking place, it is mission critical to have solutions that are not only innovative, but flexible, scalable, and complete with industry-leading support and service. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and prioritizing the needs of its customers, we strive to meet this challenge. Illumina’s innovative, array-based solutions for DNA, RNA, and protein analysis serve as tools for disease research, drug development, and the development of molecular tests in the clinic.



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