Scientist II, Molecular Biology

The ideal candidate will possess strong experimental skills and a comprehensive understanding of molecular biology. They should have experience in regulated product development, specifically in CE-IVD and IVD, and will be responsible for enhancing and developing nucleic acid purification reagents and automated workflows across diverse sample types.

Responsibilities

• Perform experiments to improve and develop nucleic acid purification reagents and automated workflows for various 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 studies through analytical validation and clinical validation phases of product development.
• Design experiments, analyze data, interpret results, and summarize data to guide product development for new product introductions, sustaining programs, and 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 customer-first mindset.
• Follow ISO 9001 and other relevant requirements.

• 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 basic chemistry and molecular biology techniques including nucleic acid extractions, quantitation and characterization, PCR techniques, and reagent/buffer preparation.
• Ability to communicate results effectively and present scientific findings.
• Strong teamwork skills and a collaborative approach.

• 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 in automated platforms such as Genexus, and other similar liquid handlers is a plus.

The position involves working Monday through Friday from 8 am to 5 pm in a highly team-oriented environment. The role may include projects across other sites and organizations, providing an opportunity for dynamic and collaborative work.

Job Type & Location

This is a Contract position based out of Austin, Texas.

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 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 Austin,TX.

Application Deadline

This position is anticipated to close on Aug 31, 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.