Associate Scientist - Purification Process Development

Lancesoft INC

Oceanside (CA)

On-site

USD 69,000 - 77,000

Full time

5 days ago
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Job summary

Lancesoft INC in Oceanside, CA is seeking an Associate Scientist – Purification Process Development to support purification process development during pivotal and commercial development phases. This onsite contract role focuses on high-throughput purification of upstream and cell culture samples and development of automated purification assays.

The candidate will execute experiments, operate automated liquid handlers (Tecan/Hamilton), analyze data, and collaborate across teams to improve

Qualifications

  • Master’s degree with 2+ years industry experience or Bachelor’s with 4+ years experience.
  • Hands-on experience in high-throughput purification assays.
  • Experience with automated liquid handling (Tecan/Hamilton).
  • Knowledge of chromatography (ÄKTA or plate-based).
  • Experience with filtration and downstream purification techniques.
  • Strong analytical and problem-solving skills; good communication.
  • Ability to work independently and in a fast-paced team.

Responsibilities

  • Execute high‑throughput purification workflows for upstream and cell culture samples.
  • Operate, optimize, troubleshoot, and maintain automated liquid handling platforms (Tecan/Hamilton).
  • Design and qualify purification assays and microscale purification methods.
  • Coordinate with upstream teams for timely sample processing and data delivery.
  • Document experiments and maintain electronic lab notebooks.
  • Collaborate with cross-functional teams to advance process development.

Skills

HT purification assays
Automated liquid handling
Chromatography knowledge
Filtration techniques
Data analysis & troubleshooting
Written and verbal communication
Independent & collaborative work

Education

Master's degree in Chemical Engineering/Biochemistry/Bioengineering or related, 2+ years industry
Bachelor's degree in related field, 4+ years industry

Tools

Tecan
Hamilton
ÄKTA or plate chromatography

Job description

Job Title: Associate Scientist – Purification Process Development

Location: Oceanside, CA 92056

Duration: 12 months+ contract

Pay Rate: 50$-56$/hr. On W2

Work Arrangement: Fully Onsite

Position Summary

We are seeking a highly motivated Research Associate II / Associate Scientist to support purification process development during pivotal and commercial development phases. This role focuses on high-throughput purification of upstream and cell culture samples, downstream process characterization, and the development and optimization of automated purification assays.

The ideal candidate will have strong hands‑on laboratory experience in high‑throughput purification, automated liquid handling systems, chromatography, and microscale purification techniques. The successful candidate will be responsible for executing experiments, troubleshooting automated workflows, analyzing data, and supporting process development initiatives in a collaborative research environment.

Key Responsibilities
High‑Throughput Purification and Automation
  • Execute high‑throughput purification workflows for upstream and cell culture samples.
  • Operate, optimize, troubleshoot, and maintain automated liquid handling platforms, including Tecan and Hamilton systems.
  • Develop, qualify, and optimize high‑throughput purification assays and microscale purification methods.
  • Coordinate with upstream teams to ensure timely sample processing and accurate data delivery.
Purification Process Development
  • Design and execute purification process development and characterization experiments.
  • Perform bench‑scale purification studies using chromatography, filtration, and microscale purification systems.
  • Support downstream process characterization and development activities.
  • Collect, analyze, interpret, and report experimental data while maintaining data integrity.
Documentation and Laboratory Operations
  • Prepare and maintain experimental protocols, technical reports, and electronic laboratory notebook records.
  • Support the implementation of new purification technologies, instrumentation, and workflow improvements.
  • Maintain laboratory equipment readiness and ensure proper laboratory organization.
  • Follow applicable laboratory safety procedures, training requirements, and quality and compliance standards.
Cross‑Functional Collaboration
  • Collaborate with upstream, downstream, and other cross‑functional teams on process development initiatives.
  • Communicate experimental progress, results, and technical challenges effectively.
  • Contribute to continuous improvement of purification methods and laboratory workflows.
Required Qualifications
  • Master's degree in Chemical Engineering, Biochemistry, Bioengineering, or a related discipline with at least 2 years of relevant industry experience; OR
  • Bachelor's degree in a related scientific or engineering discipline with at least 4 years of relevant industry experience.
  • Hands‑on experience developing and executing high‑throughput purification assays.
  • Experience operating automated liquid handling platforms such as Tecan or Hamilton.
  • Practical knowledge of chromatography, including ÄKTA or plate‑based chromatography systems.
  • Experience with filtration and standard downstream purification techniques.
  • Strong analytical, troubleshooting, and problem‑solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work independently and collaboratively in a fast‑paced research environment.
Preferred Qualifications
  • Experience with microscale chromatography and automated purification workflows.
  • Experience supporting biopharmaceutical process development and characterization.
  • Familiarity with electronic laboratory notebooks, experimental documentation, and data integrity practices.
  • Experience optimizing laboratory automation methods and troubleshooting instrumentation.
Work Environment

This is a fully onsite, laboratory‑based contract position in Oceanside, California. Candidates must be able to work onsite five days per week and perform hands‑on experimental laboratory activities.

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