Senior Associate Scientist, NGS Assay Transfer

Davita Inc.; Sorrento Valley (CA); On-site; USD 73,000 - 119,000; Full time

Job summary

A leading company in cancer detection is seeking a Senior Associate Scientist to lead method transfer activities and collaborate across departments. The role requires a strong background in life sciences, including hands-on laboratory techniques and statistical analysis. This position offers an opportunity to contribute to meaningful advancements in medical technology in a supportive and inclusive environment.

Benefits

Paid Time Off

Wellness Support

Health Benefits

Retirement Savings Plan

Qualifications

• 4+ years of experience in the life sciences industry.
• Proficient in MS Office Suite (Word, Excel, Outlook, PowerPoint).
• Authorization to work in the United States without sponsorship.

Responsibilities

• Lead and assist variety of design and test method transfer activities.
• Collaborate with departments to define test method requirements.
• Analyze data to identify trends and support troubleshooting.

Skills

Molecular Biology

Biochemistry

Biotechnology

Chemistry

Laboratory Skills

Statistical Analysis

Education

Bachelor's degree in life sciences

Advanced Degree (MS, PhD) in Biology or Chemistry

Tools

Electronic Quality Management System (EQMS)

Statistical Analysis Software (e.g., JMP, R)

Job description

Senior Associate Scientist, NGS Assay Transfer

At Exact Sciences, we're helpingchange how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others.

Position Overview

The Senior Associate Scientist, Assay Transfer role will lead and assist a variety of design and test method transfer activities within Operations. This position is primarily responsible for assisting the transfer and implementation of analytical and functional tests used to characterize and release products in operations. Additional responsibilities include collaboration with other departments to define test method requirements and development of new methods as needed.

This position is fully onsite at our San Diego office.

Include, but are not limited to, the following:

• Provide design and test method transfer support to Operations by working cross-functionally with the Production, Quality Control, Supply Chain, R&D, Systems Development, and Quality teams.
• Support test method design and transfer via test method transfer forms/plans, characterization studies, method development reports, and quality specification documents through collaboration, experiment design, study execution, data analysis, and reporting.
• Lead and assist in training and knowledge transfer of test method development and execution.
• Strong knowledge base in Molecular Biology, Biochemistry, Biotechnology, Chemistry, or a related field.
• Demonstrated proficiency in a variety of basic and intermediate laboratory skills and techniques.
• Program, operate, and troubleshoot complex instrumentation such as microplate readers, real-time and digital polymerase chain reaction ( PCR) instruments, next-generation sequencers, and liquid handling automation.
• Assist in development and characterization of intermediate to complex functional and analytical test methods with general knowledge of their use in operations and QC.
• Assist characterization of test method variability, design and coordinate execution of Measurement System Analysis (MSA) studies and determine specifications for simple measurement systems.
• Apply basic statistical techniques: assessing data normality, control charting and data trending, hypothesis testing, assessing variation, basic linear regression and model fitting, DOE, MSA, Multivariate Analysis, and ANOVA.
• Analyze data to identify trends, assists/leads troubleshooting and root cause investigation efforts with ability to utilize recognized root cause analysis tools.
• Assist investigations into analytical and functional assays and associated equipment and during the transfer process of methods into operations.
• Clearly and accurately generate experimental protocols, draft work instruction procedures, test methods, and summarize development activities through technical summary reports.
• Support Process Validation and support Test Method Validation readiness and execution. Provides support and review in generating Validation documentation.
• Write new and edit existing Quality System documents (e.g. work instructions, standard operating procedures). Identify Continuous Improvement opportunities for the Quality System. Responsible for generating/driving corrective actions/action plans for more complex changes.
• Experience using Electronic Quality Management System (EQMS) software (Agile preferred).
• Regularly coordinate activities or lead smaller sub projects. Generate project plans, identify risk, and communicate status to stakeholders.
• Lead team execution toward project milestones according to project timelines and apply recognized project management and scheduling tools.
• Determine timelines and consistently hit deliverables and commitments.
• Exercise ability to proactively plan with the ability to navigate through ambiguity and thrive in a fast-paced, frequently changing, and evolving environment.
• Understanding of continuous improvement methodologies/principles.
• Function independently with limited guidance from supervisor as well as part of a team.
• Exercise excellent oral and written communication, interpersonal, and presentation skills with strong attention to detail.
• Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
• Support and comply with the company's Quality Management System policies and procedures.
• Maintain regular and reliable attendance.
• Ability to act with an inclusion mindset and model these behaviors for the organization.
• Ability to work nights and/or weekends, as needed.
• Ability and means to travel between local Exact Sciences location(s).
• Ability to travel 5% of working time away from work location, may include overnight/weekend travel.

Minimum Qualifications

• Bachelor's degree in life sciences or field related to the essential duties of the job.
• 4+ years of experience in the life sciences industry. Master's or Doctoral degrees may be considered in lieu of 2 years of experience.
• Proficient in MS Office Suite (Word, Excel, Outlook, PowerPoint).
• Demonstrated ability to perform the essential duties of the position with or without accommodation.
• Authorization to work in the United States without sponsorship.

Preferred Qualifications

• Proficiency with statistical analysis software and/or programing (e.g. JMP, R).
• Advanced Degree in Biology, Chemistry, or similar discipline (MS, PhD).
• Experience working within an FDA 21 CFR 820, ISO 13485, ISO12207, and/or cGMP structured environment.
• Experience developing automated liquid handling workflows on Hamilton robotic platforms.
• Experience with in-vitro diagnostic product development, design transfer, manufacturing, or product support.

Help us change lives

At Exact Sciences, we're helpingchange how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others.

Position Overview

The Senior Associate Scientist, Assay Transfer role will lead and assist a variety of design and test method transfer activities within Operations. This position is primarily responsible for assisting the transfer and implementation of analytical and functional tests used to characterize and release products in operations. Additional responsibilities include collaboration with other departments to define test method requirements and development of new methods as needed.

This position is fully onsite at our San Diego office.

Essential Duties

Include, but are not limited to, the following:

• Provide design and test method transfer support to Operations by working cross-functionally with the Production, Quality Control, Supply Chain, R&D, Systems Development, and Quality teams.
• Support test method design and transfer via test method transfer forms/plans, characterization studies, method development reports, and quality specification documents through collaboration, experiment design, study execution, data analysis, and reporting.
• Lead and assist in training and knowledge transfer of test method development and execution.

• Strong knowledge base in Molecular Biology, Biochemistry, Biotechnology, Chemistry, or a related field.
• Demonstrated proficiency in a variety of basic and intermediate laboratory skills and techniques.
• Program, operate, and troubleshoot complex instrumentation such as microplate readers, real-time and digital polymerase chain reaction ( PCR) instruments, next-generation sequencers, and liquid handling automation.
• Assist in development and characterization of intermediate to complex functional and analytical test methods with general knowledge of their use in operations and QC.
• Assist characterization of test method variability, design and coordinate execution of Measurement System Analysis (MSA) studies and determine specifications for simple measurement systems.
• Apply basic statistical techniques: assessing data normality, control charting and data trending, hypothesis testing, assessing variation, basic linear regression and model fitting, DOE, MSA, Multivariate Analysis, and ANOVA.
• Analyze data to identify trends, assists/leads troubleshooting and root cause investigation efforts with ability to utilize recognized root cause analysis tools.
• Assist investigations into analytical and functional assays and associated equipment and during the transfer process of methods into operations.

• Clearly and accurately generate experimental protocols, draft work instruction procedures, test methods, and summarize development activities through technical summary reports.
• Support Process Validation and support Test Method Validation readiness and execution. Provides support and review in generating Validation documentation.
• Write new and edit existing Quality System documents (e.g. work instructions, standard operating procedures). Identify Continuous Improvement opportunities for the Quality System. Responsible for generating/driving corrective actions/action plans for more complex changes.
• Experience using Electronic Quality Management System (EQMS) software (Agile preferred).
• Regularly coordinate activities or lead smaller sub projects. Generate project plans, identify risk, and communicate status to stakeholders.
• Lead team execution toward project milestones according to project timelines and apply recognized project management and scheduling tools.
• Determine timelines and consistently hit deliverables and commitments.
• Exercise ability to proactively plan with the ability to navigate through ambiguity and thrive in a fast-paced, frequently changing, and evolving environment.
• Understanding of continuous improvement methodologies/principles.
• Function independently with limited guidance from supervisor as well as part of a team.

• Exercise excellent oral and written communication, interpersonal, and presentation skills with strong attention to detail.
• Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
• Support and comply with the company's Quality Management System policies and procedures.
• Maintain regular and reliable attendance.
• Ability to act with an inclusion mindset and model these behaviors for the organization.
• Ability to work nights and/or weekends, as needed.
• Ability and means to travel between local Exact Sciences location(s).
• Ability to travel 5% of working time away from work location, may include overnight/weekend travel.

Minimum Qualifications

• Bachelor's degree in life sciences or field related to the essential duties of the job.
• 4+ years of experience in the life sciences industry. Master's or Doctoral degrees may be considered in lieu of 2 years of experience.
• Proficient in MS Office Suite (Word, Excel, Outlook, PowerPoint).
• Demonstrated ability to perform the essential duties of the position with or without accommodation.
• Authorization to work in the United States without sponsorship.

Preferred Qualifications

• NGS lab experience.
• Proficiency with statistical analysis software and/or programing (e.g. JMP, R).
• Advanced Degree in Biology, Chemistry, or similar discipline (MS, PhD).
• Experience working within an FDA 21 CFR 820, ISO 13485, ISO12207, and/or cGMP structured environment.
• Experience developing automated liquid handling workflows on Hamilton robotic platforms.
• Experience with in-vitro diagnostic product development, design transfer, manufacturing, or product support.

#LI-AN1

Salary Range:

$73,000.00 - $119,000.00The annual base salary shown is for this position located in US - CA - San Diego on a full-time basis. In addition, this position is bonus eligible, and is eligible to be considered for company stock at hire and on an annual basis.

Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits.

Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here .

Not ready to apply? Join our Talent Community to stay updated on the latest news and opportunities at Exact Sciences.

We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, and any other status protected by applicable local, state, or federal law.

To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub. The documents summarize important details of the law and provide key points that you have a right to know.