Agilent's Companion Diagnostics Business (CDx) partners closely with leading pharmaceutical companies to develop, manufacture and commercialize in vitro diagnostic devices, which are a critical part of precision medicine. The CDx business serves to support the development of targeted cancer therapies. See http://www.agilent.com/en-us/dako-products for details.
Be a part of the future of Precision Medicine! Our mission is to improve the human condition by bringing the power of precision medicine to labs, partners and patients globally.
Want to build a career in a dynamic, results-focused environment? Join the team that's providing technical design support for R&D products, recommends changes and formulates techniques that enhance design for performance. Here, you'll work on technical design support assignments and provide solutions, learning continuously through ongoing training and on-the-job experience.
We are looking for a hardworking and dedicated representative level research assistant to join our CDx Research and Development Department. You will provide research support to develop accurate, robust, and precise assays. Your challenge will be to create value for Agilent through innovative ideas that either create new businesses or enhance existing ones. You will work in a cross-functional team dedicated to the design and development of CDx assays in a highly regulated environment and perform the following activities:
Responsibilities include:
Supporting Stability Research Associates in the planning, execution, and documentation of stability studies for Companion Diagnostic (CDx) assays and assays in feasibility.
Performing laboratory activities in accordance with Quality Management System (QMS), Good Laboratory Practice (GLP), and Good Documentation Practice (GDP) requirements.
Preparing, organizing, labeling, tracking, and maintaining study samples, reagents, supplies, and laboratory records.
Assisting with the execution of stability studies, including reagent stability, cut section stability, stained slide stability, and related studies.
Maintaining accurate and traceable laboratory documentation using electronic lab notebook system and controlled forms.
Recording experimental observations, collecting data, and communicating study progress, issues, and observations to the assigned Study Responsible and broader team.
Supporting multiple studies simultaneously while maintaining organization, accuracy, and attention to detail.
Following established procedures, protocols, and work instructions while recognizing and escalating discrepancies, unexpected results, or quality concerns.
Assisting with laboratory organization, inventory management, and other operational tasks that support study execution.
Collaborating with Stability team members and cross-functional partners to support project deliverables and timelines.
Contributing to continuous improvement efforts, including updates to templates, workflows, documentation tools, and knowledge repositories.
Participating in project team meetings to provide study updates and communicate laboratory observations.
May assist with data analysis, preparation of study summaries, protocol development, report generation, or presentation materials under the guidance of a Research Associate/Study Responsible.
Maintaining technical knowledge through training, scientific literature review, and participation in team learning activities.
This position is Hybrid requiring at least 3 on-site days per week, with additional on-site days as needed based on company needs.
BS/BA or MA in Biology, Biochemistry or related field
Ability to follow Quality System regulations including Design Control
Experience with immunohistochemistry and microscopy
Demonstrated problem-solving skills
Detail-oriented and organizational skills
Analytical skills and creativity
Proficient with Microsoft Office
Demonstration of excellent verbal and written communication
Ability to work both independently and within a team setting
Preferred Qualifications:
Background in biology techniques including immunohistochemistry, in situ hybridization, fluorescent techniques, protein biochemistry; cell biology and molecular biology
Background in one or more of the following: tumor biology, immunology, and histology
Experience with assay/protocol development
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least July 21, 2026 or until the job is no longer posted.
The full-time equivalent pay range for this position is $27.90 - $43.60/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations
Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email
[email protected] or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.
Occasional
Day
No End Date
R&D
