Sr Biochemistry Scientist Full-time

Senior Biochemistry Scientist

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.

Illumina is looking for a Senior Biochemistry Scientist to join our Test Method Engineering team! In your future role at the Madison site of the global front-runner in genetic sequencing, you will be one of a group of scientists who produce the fuel for Illumina's sequencing, which is used in the study of genetic variation and function in realms from cancer research to agriculture.

As part of a diverse, self-directed team, you will be responsible for driving method development and validation activities in a cGMP laboratory for analysis of a broad range of enzymes using state-of-art processes and equipment. You will also contribute to team driven improvement initiatives, engage in a curious and science-focused environment, and collaborate closely with cross-functional teams. We want your talent, genuine curiosity about applied science, enthusiasm for creative problem-solving, and drive to get things done.

Job duties include, but are not limited to:

• Responsible for the development, optimization, characterization, and transfer of biochemical and enzymatic assays to support manufacturing operations.
• Independently operate, maintain, and train others on key laboratory equipment platforms including fragment analyzers, microplate readers, HPLCs, PCRs, and Tape Station units.
• Prepare method transfer documentation and lead method transfer activities to internal and external laboratories, ensuring reproducibility and compliance with quality standards.
• Perform data processing, statistical evaluation, and interpretation of experimental results. Prepare technical reports, presentations, and documentation in accordance with internal GMP quality systems.
• Work closely with Quality Control, Manufacturing, Quality Assurance, Process Development, and global partner sites to support project execution.
• Work independently and collaboratively as part of a scientific team and participate in team meetings and initiatives.
• Edit and revise area work instructions and standard operating procedures (SOPs)
• Contribute to investigation and resolution of technical issues.
• Assist with continuous improvement and sustaining activities.
• Perform analyses of processes, identify gaps and deficiencies, and proactively propose practical, data driven solutions.
• Maintain organization and inventory of lab supplies, equipment, and reagents.
• Ability to lift 40 lbs. in weight and stand for periods of time during the manufacturing processes.
• Other duties that may be requested by management.

Requirements:

• 6+ years of industry relevant laboratory experience in biotechnology, biomedical, biochemical or pharmaceutical industry.
• Advanced HPLC experience with proficiency in method development/optimization, assay validation and assay characterization.
• Demonstrated ability to learn quickly and take initiative.
• Demonstrated expertise in enzymatic assays and biochemical characterization techniques.
• Excellent laboratory, organizational, and research skills.
• Demonstrated ability to work on a diverse team.
• Effective communicator with the ability to interface across functions.
• Experienced in problem-solving and reasoning skills.
• Proficient in Microsoft Word, PowerPoint & Excel.

Education:

• Typically requires a degree in biochemistry, chemistry, biology, or related field. Bachelor's degree with a minimum of 6+ years of relevant industry experience or Master's degree with a minimum of 4+ years of relevant industry experience or PhD with 2+years of relevant industry experience preferred.