Sr Validation Engineer

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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.

Position Summary:

This individual will work in a dynamic team-oriented environment and has primary responsibility for defining, implementing and maintaining validation for manufacturing processes and systems.

As a Sr Validation Engineer, you will have a strong process development or process engineering background and is able to work independently requiring minimal direction.

Additionally, this role will partner cross-functionally and cross-site with R&D, Quality, Facilities, Production, and other engineering groups to lead validation efforts, collaborate in developing validation strategies, and execute validation deliverables.

Position Responsibilities:

Represent the Consumable Validation group in a cross functional project teams, ensuring validation requirements and deliverables are communicated to the teams

Develop and articulate robust strategies for validation of processes and systems through development and release of holistic validation plans

In collaboration with end users, process owners, Quality Engineers and other team members, develop validation protocols and oversee execution of IQ, OQ, PQ for manufacturing processes and systems

Lead investigations or troubleshooting discrepancies/deviation encountered during commissioning and qualification

Write reports summarizing results and statistics for all equipment and process validation projects

Be accountable for timely completion of all validation deliverables in accordance with project timelines

Learn and understand the applicable technology and engage in technical discussions

Provide consultation to other departments performing validation activities

Provide input for creation of requirements documents

Actively participate in creation of risk management documents such as pFMEA for systems and processes

Participate as required in regulatory inspections/internal audits and develop strategies for key validation topics

Perform job function in compliance with the internal procedures and applicable external regulations and standards, e.g. FDA QSR, ISO-13485

Initiate and execute controlled document change requests

Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position.

Changes to individual responsibilities may occur due to business needs.

Position Requirements:

Minimum 5 years of related Validation experience in the life science industry (i.e. medical device/IVD, pharmaceutical, biotech)

Knowledge and working application of FDA and cGMP requirements

Intermediate knowledge and working application of validation principles and guidelines and industry practice, FMEA, and Risk Management

Knowledge and application of statistical techniques as a decision-making tool and practical experience in use of statistical analysis software JMP are highly desirable

Proficient knowledge and working application of standard operating procedures, as well as process and system validation principles for regulated industries including: FDA cGMP; ISO 13485, ISO 14971, IVDD, FMEA, Risk Analysis and Design Controls and relevant regulations and requirements

Demonstrated ability to accomplish goals in collaboration with cross-functional teams

Experience with a high volume, consumable production process is highly desired

Experience with product development processes and project management is a plus

Experience with quality and process improvement methodologies and tools (Lean, Six Sigma, value stream mapping, FMEAs, DMAIC) is desired

Excellent interpersonal and written skills; highly effective communication, facilitation, negotiation and teamwork skills are required

Computer competency in MS Office Suite (Word, PowerPoint, Excel)

Adaptable to fast-paced, dynamic work environment with ability to manage projects methodically.

Familiar with the ALCOA concept

Demonstrated understanding and use of statistical methods in experiment design, data analysis, validation, and process monitoring

Demonstrated analytical problem-solving skills in self-directed manner and must be able to work on problems of a complex scope

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 To learn more, visit: .

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.