- Perform experiments to improve and develop nucleic acid purification reagents and automated workflows for a variety of sample types, including whole blood, plasma, FFPE, and urine.
- Conduct laboratory bench work focusing on sample preparation and sequencing to support the development of targeted sequencing assays.
- Participate in various studies through the analytical validation and clinical validation phases of product development.
- Design experiments, perform basic data analysis, interpret and summarize data to guide product development for new product introductions, sustaining programs, and/or CDx programs.
- Prioritize daily activities to ensure timely completion of tasks and projects.
- Collaborate closely with cross-functional teams including bioinformatics, engineering, product management, manufacturing, and regulatory affairs to deliver high-quality results.
- Maintain accurate and detailed lab notebooks and appropriate documentation.
- Support on-market product and manufacturing troubleshooting with a strong customer-first mindset.
- Follow ISO 9001 requirements.
- Proficient in molecular biology, sample preparation, and sequencing.
- Experience in basic chemistry and molecular biology techniques, including nucleic acid extractions, quantitation and characterization, PCR techniques, and reagent/buffer preparation.
- Team player with excellent communication and presentation skills.
- Ability to design experiments and communicate results effectively.
- Minimum 3 years of relevant experience or a Master's degree in Biology/Molecular Biology or a related field with at least 1 year of relevant experience.
- Solid knowledge of next-generation sequencing.
- Experience in IVD product development is advantageous.
- In-depth understanding of genomics and cancer biology.
- Familiarity with regulatory feedback or guidance documents to support study designs.
- Experience with automated platforms such as Genexus or similar liquid handlers is a plus.
The position operates Monday through Friday, from 8 am to 5 pm. The work environment is very team-oriented and involves collaboration on projects for other organizations across different sites.
Pay and Benefits The pay range for this position is $35.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your jobclassification 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 Austin,TX. Application Deadline This position is anticipated to close on Sep 2, 2025. 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email ... for other accommodation options.