QC Associate 4

Illumina • San Diego, CA

4d • $28 - $41

About The Position

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. Job Summary: This role is responsible for performing quality control activities that support the release, characterization, and ongoing evaluation of purchased raw materials, intermediates, and finished goods. The position combines hands‑on laboratory testing with data analysis, documentation, and cross‑functional collaboration to ensure materials meet established specifications.

Requirements

• Ability to work effectively in warehouse environments, including exposure to cold and freezer temperatures.
• Proficiency with Microsoft Office tools (Excel, Word, and PowerPoint) essential.
• Excellent cross-functional collaboration, soft influence, written and verbal communication skills
• Molecular biology laboratory skills such as multichannel pipetting, etc. required.
• Ability to author and revise work instructions and perform assays with little guidance.
• Ability to respond quickly to shifting priorities and meet deadlines.
• Works on assignments requiring considerable judgment and initiative.
• Understands implications of work and makes recommendations for solutions.
• Determines methods and procedures on new assignments, typically has team leader responsibility.
• Typically requires a Bachelor’s degree and at least 1-2 years of previous related experience, 4 to 6 years of appropriate lab/industry experience may substitute for a degree.

Responsibilities

• Inspect of purchased raw materials, intermediates, and finished goods, according to established procedures.
• May perform routine and non-routine analytical, biochemical, and molecular biology assays to support release, characterization and testing of purchased raw materials, production intermediates, and finished goods.
• Analysis of data generated by functional assays.
• Assist with or may lead projects around QC process improvements and qualification of changes using project management tools to achieve timelines on multiple projects with a high level of independence.
• May participate in developing and validating analytical and functional testing methodology, revising and updating work instructions and supporting documentation.
• Work with test method development, MTT, and QA in the transfer of new QC test methods.
• May participate in lab execution of experiments for technical support of production testing including OOS (out of specification) and NC investigations, root cause analysis and CAPA activities.
• 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.

Benefits

• all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package
• We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off.
• We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 1,001-5,000 employees