Research Associate

Actalent Inc

  • Carlsbad, CA
  • 3 days ago
  • $27–$31 Per Hour

Highlights

We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Numbers & Facts

LocationCarlsbad, CA
Salary$27–$31 Per Hour

Description

Research Associate - Molecular Diagnostics & IVD Development

Position Summary

We are seeking a highly motivated Research Associate to support the development of next-generation in vitro diagnostic (IVD) products and molecular diagnostic assays. In this role, you will work closely with Scientists, Senior Scientists, and Engineers to design, execute, and optimize experiments focused on DNA- and RNA-based detection technologies.

The ideal candidate brings strong hands-on laboratory experience in molecular biology techniques, including PCR-based assays, nucleic acid extraction, and assay development. This position offers the opportunity to contribute directly to innovative diagnostic solutions that improve healthcare outcomes and global health initiatives.

Key Responsibilities

  • Support product development activities for molecular diagnostic and IVD programs under the guidance of Senior scientific staff.
  • Design, execute, and optimize experiments to evaluate assay performance on both benchtop platforms and integrated disposable devices.
  • Develop and improve DNA- and RNA-based assays to meet analytical performance, sensitivity, specificity, and reliability targets.
  • Analyze experimental data, draw meaningful conclusions, and recommend next steps to advance project objectives.
  • Troubleshoot assay, reagent, and device-related performance issues using a data-driven and scientific approach.
  • Maintain accurate experimental records and comply with Good Documentation Practices (GDP) to ensure traceability and reproducibility.
  • Prepare technical reports, summaries, graphs, and presentations to communicate findings to cross-functional teams.
  • Collaborate with scientists and engineers to integrate assays into automated device platforms.
  • Perform routine molecular biology, microbiology, and sample preparation procedures while adhering to laboratory safety and aseptic practices.
  • Manage multiple projects and priorities in a fast-paced product development environment.
  • Contribute innovative ideas that enhance assay performance, workflow efficiency, and product design.

Required Qualifications

Education

  • Bachelor"s or Master"s degree in Molecular Biology, Biology, Biochemistry, Microbiology, Biotechnology, or a related Life Sciences discipline.

Experience

  • Minimum 2 years of hands-on laboratory experience in molecular biology, assay development, or diagnostic product development.
  • Experience designing, executing, and analyzing laboratory experiments independently.
  • Proven ability to document, organize, and communicate scientific results effectively.

Technical Skills

  • Strong understanding of molecular biology, biochemistry, microbiology, immunology, or related scientific disciplines.

  • Hands-on experience with:

  • PCR, qPCR, and/or digital PCR

  • Nucleic acid extraction and sample preparation

  • DNA and RNA assay development

  • Bacterial culture and microbiology techniques

  • Laboratory instrumentation and data analysis software

  • Proficiency with Microsoft Office applications, especially Excel, Word, and PowerPoint.

Core Competencies

  • Strong analytical thinking and problem-solving skills.
  • Ability to troubleshoot complex technical challenges.
  • Excellent organizational and time-management abilities.
  • Effective verbal and written communication skills.
  • Demonstrated ability to work both independently and collaboratively within multidisciplinary teams.

Preferred Qualifications

  • Experience supporting IVD or medical device product development programs.
  • Familiarity with assay optimization, validation, and verification activities.
  • Experience with automated workflows, microfluidics, or disposable diagnostic devices.
  • Knowledge of spectrophotometry, buffer formulation, and reagent development.
  • Experience presenting scientific findings to technical and non-technical audiences.
  • Exposure to regulated environments, including design control or quality system processes.
  • Passion for advancing molecular diagnostics and improving global health outcomes.

Job Type & Location

This is a Contract position based out of Carlsbad, CA.

Pay and Benefits

The pay range for this position is $27.00 - $31.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Carlsbad,CA.

Application Deadline

This position is anticipated to close on Aug 11, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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