Microbiologist

Position Title: Microbiologist - Research and Development (Evening and Weekend Shifts) We are seeking a Microbiologist with hands-on experience in Research and Development to join our team.

This role requires evening availability from 2:30 PM to 11:00 PM on Wednesday, Thursday, and Friday, and daytime availability from 10:00 AM to 7:00 PM on Saturday and Sunday.

As a member of the Microbiology team, you will play a critical role in supporting the development and commercial readiness of our products.

You will be responsible for designing, documenting, and testing instruments and consumables, executing protocols, and preparing detailed reports.

Your contributions will directly impact the success of our product lines and overall company performance.

Primary Responsibilities: + Conduct microbiological testing to support ongoing study protocols and evaluate new instruments, AST panels, and consumables + Analyze assay data daily and ensure accurate documentation + Inspect incoming consumables for quality and compliance + Process biological specimens using aseptic techniques and adhere to laboratory safety standards + Collaborate with cross-functional teams and departments to support project goals + Prepare and present reports on experimental results and failure investigations + Participate in routine laboratory operations, including experiment execution, equipment maintenance, cleaning, and standard testing procedures + Perform additional duties and contribute to departmental projects as assigned by management Experience Requirements: + Bachelor's degree in Microbiology or a related scientific discipline + Demonstrated experience in microbiological testing, data analysis, and laboratory operations + Familiarity with aseptic techniques and lab safety protocols + Proven ability to coordinate with cross-functional teams + Experience in preparing technical reports and conducting failure investigations + Comfortable working in a fast-paced, regulated laboratory environment Knowledge, Skills, and Abilities: + Strong understanding of aseptic techniques, Good Documentation Practices (GDP), and Good Laboratory Practices (GLP) + Proficiency in Microsoft Office applications, including Word, Excel, and PowerPoint + High attention to detail with a commitment to accuracy and quality + Ability to adapt to shifting priorities and work under time constraints + Strong organizational, communication, and troubleshooting skills + Capable of working independently after initial training + Familiarity with ISO 9001 and FDA Quality System Regulations is a plus Pay and Benefits The pay range for this position is $22.00 - $28.00/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 San Jose,CA.

Application Deadline This position is anticipated to close on Oct 7, 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.