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Research Associate, Analytical Development

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Halozyme Hypercon
Full Time position
Listed on 2026-07-03
Job specializations:
  • Research/Development
    Research Scientist
Salary/Wage Range or Industry Benchmark: 58000 - 80000 USD Yearly USD 58000.00 80000.00 YEAR
Job Description & How to Apply Below

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 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 Research Associate, Analytical Development plays a key role in supporting the characterization and evaluation of drug product particulates using microscopy and spectroscopic techniques. This position executes routine analytical testing, ensures accurate data documentation in a regulated environment. Through strong attention to detail and collaboration with cross‑functional teams, this role contributes to reliable analytical results and overall advancement of the analytical program.

In

this role, you’ll have the opportunity to:
  • Perform routine analytical characterization of particles under established methods, including microscopy techniques such as flow imaging microscopy to assess particle size, concentration, identification, and morphology.
  • Execute visual inspection to assess drug product defects.
  • Operate, maintain, and perform routine troubleshooting of analytical instrumentation (e.g., microscopes), including preparation 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 qualification activities by executing assigned experiments and providing data and observations to supervising scientists.
  • 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 Chemical or Biological Engineering, Chemistry, Pharmaceutical Sciences, or a related discipline with 0–2 years of relevant industry experience.
  • Hands‑on experience with microscopy techniques. Preferably for characterization of particle.
  • Experience with spectroscopic and other biophysical techniques is a plus (e.g., FTIR, circular dichroism, analytical ultracentrifugation).
  • Experience with difficult‑to‑inspect parenteral products (e.g., suspensions, emulsions) is a plus.
  • Working knowledge of data analysis and visualization tools, including Microsoft Excel, JMP, or Graph Pad Prism. Experience with Python or R for advanced data analysis is desirable.
  • 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.
  • 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 Program and 401(k) matching.
  • Opportunities to grow in a culture that prioritizes…
Position Requirements
10+ Years work experience
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