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.

Are you the leader that Illumina is looking for!?

In this impactful leadership role you'll lead a talented team of scientists responsible for the end-to-end lifecycle for test methods that ensure a consistent delivery of quality materials that fuel Illumina’s sequencing and array-based solutions for analysis of genetic variation and function, in realms from cancer research to agriculture. 

Your positive energy, genuine passion for leadership, and commitment to cross-functional success will undoubtedly help us to deliver on our global mission to improve human health! #Illuminaproud ##unlockthepowerofthegenome

Responsibilities:

Manage the lifecycle (e.g. development, characterization, transfer, sustaining and end of life) for Test Methods supporting enzyme and reagent manufacturing, lyophilization, and material investigations.

Drive timely execution of test events supporting product release.

Own and ensure maintenance of the real time stability program.

Continuously monitor departmental resourcing needs, driving talent acquisition activities when necessary, aligning to budget.

Represent the Quality Control function within core teams and other extended New Product Introduction teams.

Provide ongoing guidance and career counseling supporting employee development.

Align departmental goals with site level strategy.

Establish realistic performance standards and leverage performance appraisals to identify performance improvement opportunities.

Guide and mentor individuals on the design and execution of controlled experiments, optimizing the critical process parameters affecting assay variability for test methods used within a cGMP environment.

Develop methodology to effectively implement continuous improvement, and operational excellence, mechanisms (e.g. automated statistical process controls).

Maintain job descriptions to accurately represent the primary responsibilities, qualifications, and terms for each role within the team.

Staff and train employees to all applicable company policies and procedures.

Listed responsibilities are an essential, although not exhaustive, list of the usual duties associated with this position.  Changes to individual responsibilities may occur due to business needs.

Experience / Knowledge Requirements:

10+ years of Manufacturing / Operations experience, including 5+ years of team management experience.

Demonstrated success building, leading, and influencing diverse cross-functional teams.

Able to apply knowledge to influence other stakeholders on desired departmental outcomes.

Able to persuade others in sensitive and complex situations while preserving relationships.

Exceptional communication skills, both written and verbal.

Preferred Educational Background:

Bachelor’s, Master’s, or Ph.D. in Biology, Chemistry, or related discipline.

The estimated base salary range for the Sr. Manager, QC Analysis role based in the United States of America is: $128,600 - $193,000. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, 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.

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 accommodations@illumina.com. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. This role is not eligible for visa sponsorship.