QC Analyst 1

What if the work you did everyday 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.

The Quality Control Analyst will work as part of the Reagent QC team to support Reagent QC operations. The individual will be responsible for testing and releasing Illumina reagents in a fast-paced, GMP regulated environment, maintaining stock of consumables in the lab, collaborating with other departments for production and non-production processes, as well as maintain a strong working relationship with supply chain and other partner organizations.

Responsibilities:

• Day to day management of a production process, management of a process flow that occurs across several departments.
• Maintains health of laboratory inventory by pulling Kanban cards, ordering materials, and expediting urgent requests.
• Perform routine and non-routine analytical biochemical and molecular biology assays to support release, characterization and stability testing of raw materials, production intermediates and final goods.
• Analysis of data generated by functional assays.
• Participate in developing and validating testing methodology, revising and updating Standard Operating Procedures.
• Review data obtained for compliance to specifications and report abnormalities.
• Attends and participate in team meetings.
• 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.

Requirements:

• Ability to understand and follow work instructions and perform molecular biology assays with little guidance.
• Proficiency with Microsoft Office tools (Excel, Word, and PowerPoint)
• Self-starter, strong work ethic, strong organizational skills, strong communication skills, critical thinking, attention to detail and accuracy, the ability to work independently and in a team environment, a are essential.
• GMP experience a plus
• Knowledge of the following:
• PCR
• Gel extraction
• cDNA synthesis
• Basic Genetics
• Basic statistical analysis techniques
• Microarray assays and technology
• Knowledge of ISO and FDA requirements preferred.
• Experience with large data sets a plus
• Experience with robotics a plus
• Experience with Illumina products also a plus
• All listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities

Experience/Education:

• Typically requires a minimum of 2 - 4 years of related experience
• High School Diploma required

Concerns regarding COVID-19 continue as positive cases are experienced in the communities in which we operate. Please be aware that, as a condition of employment, Illumina may require proof of COVID vaccination in accordance with local statutory requirements (subject to limited exceptions) beginning November 1, 2021.

At Illumina, we strive to foster a diverse and inclusive workplace by cultivating an environment in which everyone contributes to our mission. Built on a strong foundation, Illumina has always been rooted in openness, collaboration, and seeking alternative views and 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 demonstrate our collective commitment to diversity and inclusion in the communities we live and work. 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. If you require accommodation to complete the application or interview process, please contact [email protected]. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf