Senior Scientist

1 Year ago • 3-5 Years • Research Development • $111,000 PA - $166,600 PA

Job Summary

Job Description

Illumina Laboratory Services (ILS) is seeking a Senior Scientist to join their development and validation team. This role involves developing and validating a variety of workflows and processes for clinical and research use in genomics and multiomics. The Senior Scientist will collaborate with automation development, software development, bioinformatics, process engineering, quality assurance, and operations groups. Key responsibilities include supporting development and validation in CLIA, CAP, and ISO13485 compliant environments, leading experiments, analyzing data, writing reports, and facilitating the transfer of technologies to the CLIA laboratory. The ideal candidate will have experience in molecular biology methods, nucleic acid applications, sequencing, and interfacing with cross-functional teams in a clinical laboratory setting.
Must have:
  • Support development and validation in CLIA, CAP, ISO13485.
  • Lead experiments, analyze data, write reports.
  • Apply DOE methods and plan activities.
  • Transfer NGS/Array technologies to CLIA lab.
  • Collaborate with cross-functional groups.
  • Provide technical issue resolution.
  • Work with sample prep, library prep, sequencing.
  • Support training of lab staff.
  • Act as technical representative.
  • Troubleshoot existing processes.
  • 5 years experience with Bachelor's or 3 years with Master's.
  • Knowledge of NGS, PCR, microarrays.
  • Excellent experimental design and data analysis skills.
  • Demonstrated technical proficiency and creativity.
  • Ability to learn new technologies quickly.
  • Strong written and verbal communication skills.
  • Detail-oriented, organized, self-motivated.
  • Collaborative and adaptable to fast-paced environments.
Good to have:
  • Clinical experience developing or validating assays.
  • Background in sequencing, NIPT, proteomics, oncology.
  • Experience with design controls, risk management.
  • Experience with validation/verification study design.
  • Hands-on experience with next-generation sequencing.
  • Experience with automation/liquid handling robots.
  • Knowledge of NGS secondary analysis and data analysis tools.

Job Details

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.

llumina Laboratory Services (ILS) is an exciting and rewarding organization that applies Illumina’s core sequencing and array technology to sustain existing Illumina’s service offering while driving implementation of new assays and technologies into clinical laboratory service offering. ILS works cross functionally to meet customer demands while also exploring new offerings within the clinical space.  The Sr. Scientist role in the development and validation team of Illumina Laboratory Services will work on the development and validation of a wide range of workflows and processes for clinical and research use in the genomics and multiomics spaces.  This role will work closely with the automation development, software development, bioinformatics, process engineering, quality assurance, and operations groups. This role also will be involved in a cross-functional, cross-site collaborative team to transfer new tests and improve existing tests in Illumina’s clinical laboratory, write technical documents, and plan/execute experiments for use in development studies and validations. The ideal candidate will be able to lead appropriate multi-disciplinary investigations and resolve technical problems, have experience interfacing with cross functional teams and familiarity with the regulatory standards of clinical laboratory environment.  In addition, experience in molecular biology methods for nucleic acid applications and sequencing are required.

Responsibilities:

  • Support development and validation efforts in CLIA, CAP and ISO13485 compliant environment.

  • Lead laboratory experiments, design, and execution, analyze data, and write development and validation plans/reports as appropriate.

  • Ability to apply DOE methods, and collect requirements, plan activities, and contribute to budget of allocated project scope, and prioritization of activities/assignments to supporting team members.

  • Facilitate the transfer of NGS and/or Array technologies from development to the CLIA laboratory.

  • Collaborate with cross-functional groups including QA, Software, Bioinformatics, Process/Automation engineers, Supply chain, and Operations to launch new workflows and improve existing lab processes.

  • Support and provide guidance on technical issue resolution.

  • Work across a wide range of technologies, such as sample preparation, library prep, and next-generation sequencing.

  • Support in training laboratory staff on new workflows/protocols.

  • Be a technical and integration representative for Operations on cross functional initiatives.

  • Support and troubleshoot existing processes and may provide guidance on potential enhancements as appropriate.

All listed tasks and responsibilities are deemed essential functions to this position; however, business conditions may require reasonable accommodation for additional tasks and responsibilities.

Requirements:

  • Typically requires a minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree; or a PhD without experience; or equivalent work experience.

  • Knowledge and hands-on skills working with a variety of molecular techniques such as NGS, PCR, and microarrays.

  • Excellent skills in experimental design, implementation, troubleshooting, and data analysis.

  • Demonstrated ability for technical proficiency, scientific creativity, and independent thought.

  • Ability to quickly learn new scientific technologies.

  • Strong written and verbal communication skills. Adept at creating presentations tailored to a specific audience. Able to develop technical documents including work instructions.

  • Detail-oriented, organized, and self-motivated.

  • Collaborative in nature and a desire to be part of a fast-paced, dynamic, cross-functional environment.

Preferred:

  • Clinical experience developing or validating assays (IVD, LDT, and/or CDx) in a regulated environment.

  • Background/expertise in Sequencing, non-invasive prenatal testing, proteomics, methylation, single cell, or oncology preferred.

  • Experience with design controls, risk management, and change management preferred.

  • Prior experience with study design for validations/verifications preferred.

  • Hands-on experience with next-generation sequencing technologies is strongly preferred.

  • Experience with automation / liquid handling robots (e.g. Tecan, Hamilton, Eppendorf) is desirable.

  • Knowledge of NGS secondary analysis and data analysis software tools such as JMP or R desirable.

We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative 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 offer opportunities to engage in social responsibility. 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. 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 accommodations@illumina.com. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. 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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About The Company

At Illumina, our goal is to apply innovative technologies and revolutionary assays to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. These studies will help make the realization of personalized medicine possible. With such rapid advances in technology taking place, it is mission critical to have solutions that are not only innovative, but flexible, scalable, and complete with industry-leading support and service. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and prioritizing the needs of its customers, we strive to meet this challenge. Illumina’s innovative, array-based solutions for DNA, RNA, and protein analysis serve as tools for disease research, drug development, and the development of molecular tests in the clinic.



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