Overview
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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.
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.
Responsibilities
- Represent the Consumable Validation group in 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 internal procedures and applicable external regulations and standards, e.g. FDA QSR, ISO-13485
- Initiate and execute controlled document change requests
Qualifications
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 requirementsIntermediate knowledge and working application of validation principles and guidelines and industry practice, FMEA, and Risk ManagementKnowledge and application of statistical techniques as a decision-making tool and practical experience in use of statistical analysis software JMP are highly desirableProficient 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 requirementsDemonstrated ability to accomplish goals in collaboration with cross-functional teamsExperience with a high volume, consumable production process is highly desiredExperience with product development processes and project management is a plusExperience with quality and process improvement methodologies and tools (Lean, Six Sigma, value stream mapping, FMEAs, DMAIC) is desiredExcellent interpersonal and written skills; highly effective communication, facilitation, negotiation and teamwork skills are requiredComputer 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 conceptDemonstrated understanding and use of statistical methods in experiment design, data analysis, validation, and process monitoringDemonstrated analytical problem-solving skills in self-directed mannerCompany and equal opportunity
We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Illumina is 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.
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