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Quality Engineer

Job in Cambridge, Cambridgeshire, England, UK
Listing for: Illumina
Full Time, Contract position
Listed on 2025-11-07
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 GBP Yearly GBP 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Quality Engineer 2 page is loaded## Quality Engineer 2locations:
England - Chesterford:
England - Cambridge time type:
Full time posted on:
Posted Todayjob requisition :
41594-JOB## 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, be 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 youexpect
** Our team members are bright, energetic,…
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