Senior Research Associate, Analytical Development

Description

Welcome to an inspired career.

At Halozyme Hypercon, a wholly-owned subsidiary of Halozyme Therapeutics, Inc., we are reinventing the patient experience and building the future of drug delivery. We are passionate about the important work we do and constantly strive to do more. We embrace transformation and work hard to innovate for the future. We do this together, as One Team - we rise by lifting others up and believe in the power of working together for the collective win.

That's why we need you-to help us make a significant impact by taking on increasingly complex challenges, leaping beyond the status quo, advancing our mission and making our One Team culture thrive.

Join us as Senior Research Associate, Analytical Development and you'll be part of a culture that welcomes diversity, thinks differently to solve problems, works collaboratively as one team, and delivers meaningful innovations that impact people's lives.

How you will make an impact

The Senior Research Associate, Analytical Development plays a critical role in generating high-quality analytical data to support the characterization and development of biologic products. This role executes and supports a wide range of analytical methods, including chromatographic and electrophoretic techniques, while ensuring accuracy, compliance, and data integrity in a regulated laboratory environment. Through strong technical execution, attention to detail, and collaboration with cross-functional teams, this position contributes to method development, troubleshooting, and overall advancement of the analytical program.

In this role, you'll have the opportunity to:

* Perform routine and non-routine analytical characterization of biologics under established or developing methods, including HPLC/UPLC techniques such as Size Exclusion Chromatography (SEC) to assess aggregation and purity.

* Execute capillary isoelectric focusing (cIEF) assays to evaluate charge heterogeneity and assess product consistency, following approved methods or protocols under senior staff guidance.

* Execute and support quantitative analytical assays for surfactants and other stabilizing excipients, including sample preparation, data acquisition, and preliminary data processing.

* Perform selected microbiological assays (e.g., endotoxin testing) in accordance with approved SOPs to support product characterization and release activities.

* Operate, maintain, and perform routine troubleshooting of analytical instrumentation (e.g., HPLC/UPLC systems), including preparation of mobile phases, columns, reagents, and standards.

* Accurately document experimental procedures, observations, and results in electronic laboratory notebooks in compliance with Good Laboratory Practice (GLP) and data integrity requirements.

* Perform routine laboratory activities such as buffer formulation, reagent preparation, pipetting, and sample handling with a high degree of accuracy and attention to detail.

* Support method development, optimization, and qualification activities by executing assigned experiments and providing data and observations to supervising scientists.

* Assist with investigations of analytical issues or out?of?specification / out?of?trend results by executing defined experiments and compiling data, under the direction of senior staff.

* Collaborate with Analytical Development colleagues and cross?functional partners (e.g., Process Development, Formulation Development, Manufacturing) to support analytical testing needs.

* Ensure laboratory safety compliance, proper instrument calibration, and adherence to standard operating procedures (SOPs).

Requirements

To succeed in this role, you'll need:

* Bachelor's degree in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related discipline with 2-4 years of relevant industry experience, or Master's degree with 0-2 years of relevant experience.

* Hands-on experience with analytical techniques such as SEC, cIEF, and chromatographic quantitation assays is preferred.

* Experience operating chromatographic systems (HPLC/UPLC) and familiarity with chromatography data systems such as Waters Empower and/or Thermo Chromeleon.

* Working knowledge of data analysis and visualization tools, including Microsoft Excel, JMP, and Graph Pad Prism.

* Demonstrated ability to accurately document experimental work using electronic laboratory notebooks (ELN).

* Knowledge of GLP principles, data integrity expectations, and regulated laboratory practices.

* Ability to follow detailed experimental protocols and execute work independently within defined objectives and timelines.

* Strong organizational skills, attention to detail, and ability to work effectively in a collaborative laboratory environment.

* Effective written and verbal communication skills for reporting data and experimental observations to supervising scientists.

Travel:
May be required up to 5% of your time.

In return, we offer you:

* Full and comprehensive benefit program, including an Employee Stock Purchase…