Design Quality Engineer 2 at Illumina

San Diego, California, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, Medical DevicesIndustries

Requirements

Bachelor's Degree in Engineering and/or Science (preferred)
Master's Degree (advanced degree without experience or equivalent work experience)
PhD (advanced degree without experience or equivalent work experience)
1-3 years of related experience
1-3 years experience working within FDA/ISO regulated industry
Quality Certification (e.g. CQE) (preferred, upon hire)
Technical expertise in areas such as Assay Development, Bioinformatics, Shop Floor Operations, MFG Quality Engineering, Clinical Trials, Instrument Development (with focus on CMOS and MEMS) (preferred)
Knowledge of quality and statistical analysis tools (e.g. SPC, Six Sigma, Risk Analysis, FMEA, DOE, statistical comparison tests, trend analysis) (preferred)
Knowledge of FDA regulatory environment (CFR 820), 501k, ISO 14971, ISO 13485, and IVDR (preferred)
Team oriented with excellent communication skills
Excellent cross-functional collaboration
Detailed oriented, well organized, able to work independently and in teams
Adaptable to fast-paced, dynamic work environment with shifting demands

Responsibilities

Provides Quality oversight to ensure the company's products and processes are safe, effective, and meet customer performance needs throughout the product lifecycle
Provides support for project planning, requirements/specifications development, design verification and validation, design transfer, process development, process validation, risk management, and/or human factors
Supports product risk management activities
Supports audits to ensure the quality and completeness of product Design History Files and/or Device Master Record
Gains understanding of applicable technology to facilitate participation in the technical discussions and risk-based decision making
Provides project Quality lead and/or management with status updates on assigned responsibilities and goals and escalates issues in a timely fashion
Gains understanding of quality and statistical analysis tools (e.g. SPC, Six Sigma, Risk Analysis, FMEA, DOE, statistical comparison tests, and trend analysis)
Other such duties that may be determined by Management

Skills

Key technologies and capabilities for this role

Design ControlFDA 21 CFR 820ISO 13485ISO 14971IVDRRisk ManagementDesign VerificationDesign ValidationProcess ValidationDesign TransferHuman FactorsQuality OversightAuditsDesign History FilesDevice Master Record

Questions & Answers

Common questions about this position

What are the minimum qualifications for the Design Quality Engineer 2 role?

A Bachelor's Degree in Engineering and/or Science is preferred, with 1-3 years of related experience and 1-3 years working within an FDA/ISO regulated industry required. Master's or PhD degrees allow for advanced degrees without experience or equivalent work experience.

What key responsibilities does this role involve?

The role provides quality oversight for products and processes, supports design control activities like verification, validation, risk management, and process validation, and participates in cross-functional teams and audits.

What is the salary or compensation for this position?

This information is not specified in the job description.

Is this a remote position, or what is the location policy?

This information is not specified in the job description.

What does Illumina's company culture emphasize?

Illumina emphasizes working on impactful projects that transform human health, being part of something bigger, surrounded by extraordinary people, inspiring leaders, and world-changing projects where every role makes a difference.

Illumina

Supports genomics startups through funding and resources

About Illumina

Illumina focuses on fostering innovation in the genomics industry by supporting startups through its Illumina Accelerator program. This program helps entrepreneurs create, launch, and grow genomics-focused companies by providing funding and resources. The accelerator operates in two main locations: the San Francisco Bay Area and Cambridge, UK. Illumina Accelerator has successfully invested in 68 genomics startups, which have collectively raised over $1 billion in venture capital. What sets Illumina apart from its competitors is its strong partnership with leading venture capital investors and its dedicated focus on the genomics sector. The goal of Illumina is to build a thriving ecosystem for genomics innovation, enabling new companies to emerge and advance the field.

San Diego, CaliforniaHeadquarters

1998Year Founded

$27.2MTotal Funding

IPOCompany Stage

Venture Capital, BiotechnologyIndustries

5,001-10,000Employees

Risks

Over-reliance on NVIDIA's AI technology may limit flexibility in AI solution adoption.

Standardizing proteomics data across platforms could challenge Illumina's data reliability.

Single-flow-cell NovaSeq X System might cannibalize sales of higher-end models.

Differentiation

Illumina leads in genomic sequencing with advanced AI integration and multiomic data analysis.

The company offers innovative array-based solutions for DNA, RNA, and protein analysis.

Illumina's global expansion includes a new Global Capability Center in Bengaluru.

Upsides

Collaboration with NVIDIA enhances drug discovery and clinical development through AI integration.

Pilot proteomics program with UK Biobank aims to generate crucial reference datasets.

Single-cell sequencing kits make high-throughput sequencing accessible to smaller labs.

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