Quality Engineer 2

Illumina; Greater London; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading genomics firm in Chesterford is seeking a Quality Engineer 2. In this role, you will be responsible for applying quality regulations and collaborating with teams to ensure validation of manufacturing operations. The ideal candidate will have experience with ISO 13485, strong analytical and problem-solving skills, and an ability to work both independently and collaboratively. This one-year fixed-term position offers competitive benefits and the opportunity to contribute to impactful projects in genomic technology.

Benefits

Flexible time off

Leisure travel insurance

Employee Stock Purchasing Program

Volunteer time off

Qualifications

• Experience applying quality regulations and standards, preferably ISO 13485.
• Strong experience in change control and failure investigation.
• Experience in nonconformance and root cause investigations.

Responsibilities

• Act as the validation expert in manufacturing operations.
• Resolve issues by applying company policies and procedures.
• Ensure timely completion of validation deliverables.

Skills

Analytical skills

Problem-solving skills

Attention to detail

Organizing skills

Education

Bachelor’s degree or equivalent work experience

Job description

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.

Quality Engineer 2, Onsite in Chesterford, UK

Please note that this is a one year fixed term role

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.

Illumina's employee benefits are industry leading and include, Flexible time off, Compassion and care time off, Leisure travel insurance, Pension, Employee Stock Purchasing Program, Volunteer time off and much more!!

Why You

To be successful as our Quality Engineer 2 you will have experience applying quality regulations and standards (preferably, ISO 13485) and establishing quality systems. You will have strong analytical, problem solving and organizing skills as well as experience in change control and failure investigation environments. You will have excellent attention to detail, well organized and able to work independently as well as working collaboratively as part of the team.

Your experienced to date will include nonconformance and root cause investigations and participation in Quality Management Core processes. You will thrive in a fast-paced environment and enjoying building relationships with internal stakeholders and functions.

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

• Act as the validation subject matter expert in manufacturing operations, relevant additional value streams and project teams, ensuring validation requirements and deliverables are communicated to the teams.
• Applies company policies and procedures to resolve a variety of issues.
• Determines a course of action based on guidelines. Modifies processes and methods as required
• Works on assignments of moderate scope where problem solving requires application of learned techniques. For example, Quality Investigation, Nonconformance and CAPA processes, and validation
• Be accountable for timely completion of all validation deliverables in accordance with manufacturing needs and project timelines.
• Builds productive working relationships internally and externally.
• Provides standard professional guidance and collaborates to resolve mutual problems.
• Works autonomously and receives little instruction on day-to-day work/new assignments.
• Exercises judgment within defined procedures and practices to determine appropriate action.
• Perform job function in compliance with the internal procedures and applicable external regulations and standards, e.g. FDA QSR, ISO-13485.

Excellent attention to detail, well organized and able to work independently and as a team.

Preferred Educational and Experience Background

• Typically requires a Bachelor’s degree and some related experience; or an advanced degree without experience; or equivalent work experience.

What can you expect

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 including highly competitive salaries 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.

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.

We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. 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. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact [e-mail]. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.