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Temporary Variant Scientist Jobs in California (NOW HIRING)

Temporary Variant Scientist information

What is the difference between Temporary Variant Scientist vs Temporary Quality Control Analyst?

AspectTemporary Variant ScientistTemporary Quality Control Analyst
Required CredentialsBachelor's or Master's in Life Sciences, relevant certificationsBachelor's in Life Sciences or related field, certifications may be preferred
Work EnvironmentLaboratories, R&D settings, pharmaceutical or biotech companiesLaboratories, manufacturing facilities, quality assurance departments
Employer & Industry UsagePharmaceutical, biotech, and research organizationsManufacturing, pharmaceutical, and biotech industries
Common Search & ComparisonYesYes

The Temporary Variant Scientist and Temporary Quality Control Analyst roles both operate within laboratory and industry settings, often in pharmaceutical or biotech companies. The Variant Scientist focuses on analyzing genetic or product variants during research and development, requiring specialized scientific knowledge. In contrast, the Quality Control Analyst primarily ensures product quality through testing and compliance. While their credentials and work environments overlap, their core responsibilities differ, making each role distinct in the industry.

How much do Temporary Variant Scientists make?

Temporary Variant Scientists typically earn between $25 and $50 per hour, depending on experience, location, and the complexity of the projects. They often work in laboratory or research settings, requiring knowledge of genetic analysis and laboratory techniques.

How to become a temporary variant scientist?

To become a temporary variant scientist, typically a bachelor's degree in biology, chemistry, or a related field is required, along with experience in laboratory research and data analysis. Strong knowledge of virology, genetics, or microbiology, along with proficiency in scientific tools and techniques, is essential; some roles may require advanced degrees or certifications. Flexibility and the ability to work in fast-paced environments are also important for temporary positions.

What are the most commonly searched types of Variant Scientist jobs in California?

The most popular types of Variant Scientist jobs in California are:

What cities in California are hiring for Temporary Variant Scientist jobs?

Cities in California with the most Temporary Variant Scientist job openings:

Infographic showing various Temporary Variant Scientist job openings in California as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 79% Full Time, 14% Part Time, and 5% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Sr. Scientist, Pharmaceutical Development

San Diego, CA

Actalent
Business Management Consulting • 5 - 10K employees

$43/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New


Job description

Scientist, Pharmaceutical DevelopmentAbout the Role

We are seeking a highly motivated Scientist, Pharmaceutical Development to support biologics drug product development through hands-on laboratory experimentation, formulation development, physicochemical characterization, and analytical testing. This role offers the opportunity to contribute to the advancement of innovative biologic therapies while collaborating with cross-functional teams in a fast-paced pharmaceutical development environment.

The successful candidate will independently execute analytical studies, interpret and present scientific data, support method development initiatives, maintain laboratory instrumentation, and contribute to clinical and technology transfer activities.

Key Responsibilities
  • Perform analytical testing using HPLC, UPLC, and iCiEF techniques to support biologics characterization and development activities.
  • Prepare samples, reagents, buffers, and standards for routine and experimental testing.
  • Conduct physicochemical and protein characterization studies to evaluate product quality and stability.
  • Analyze experimental data and prepare technical reports, protocols, study summaries, and presentations.
  • Maintain accurate laboratory records and documentation in accordance with GMP and regulatory expectations.
  • Support analytical method development, optimization, qualification, and troubleshooting activities.
  • Collaborate with Analytical Development, Manufacturing, Quality, Project Management, and external partners to support drug product development programs.
  • Assist with technology transfer activities and clinical manufacturing support.
  • Maintain, calibrate, and troubleshoot laboratory equipment to ensure efficient laboratory operations.
  • Manage multiple projects and priorities while meeting development timelines.
Required QualificationsEducation & Experience
  • Bachelor's degree in Biotechnology, Biochemistry, Pharmaceutical Sciences, Chemistry, or a related scientific discipline with 4+ years of relevant industry experience; OR
  • Master's degree in a related field with 2+ years of relevant industry experience.
Technical Skills
  • Hands-on experience operating and executing methods utilizing HPLC/UPLC platforms.
  • Experience with biologics and protein characterization techniques, including:
    • Size Exclusion Chromatography (SEC)
    • Reverse Phase (RP)
    • Hydrophobic Interaction Chromatography (HIC)
    • Ion Exchange Chromatography (IEX/CEX)
    • Charged Aerosol Detection (CAD)
    • CE-SDS
    • Charge Variant Analysis
    • Particle Characterization
  • Experience with Imaged Capillary Isoelectric Focusing (iCiEF) and related charge variant characterization methods.
  • Working knowledge of biologics, protein chemistry, and analytical development principles.
  • Strong technical writing skills, including preparation of SOPs, protocols, reports, and study plans.
Preferred Qualifications
  • Experience working in a regulated pharmaceutical, biotechnology, or biologics development environment.
  • Familiarity with GMP documentation practices and regulatory expectations.
  • Strong organizational, problem-solving, and project management skills.
  • Ability to work independently while effectively collaborating with multidisciplinary teams.
  • Experience supporting multiple concurrent drug development programs.
Work Environment
  • Fully onsite laboratory position.
  • Monday through Friday, approximately 8:00 AM – 5:00 PM.
  • Collaborative environment working closely with Analytical Development, Manufacturing, Quality, Project Management, and external stakeholders.
  • Fast-paced setting supporting biologics development and clinical manufacturing activities.
  • Contract assignment anticipated to last approximately 5 to 7 months.
  • Two-stage interview process.
Why this position?

This is an excellent opportunity to contribute to cutting-edge biologics development while gaining exposure to analytical characterization, formulation development, technology transfer, and clinical manufacturing support. You will work alongside experienced scientific professionals and have a direct impact on advancing innovative therapies from development to clinical application.

Job Type & Location

This is a Contract position based out of San Diego, CA.

Pay and Benefits

The pay range for this position is $43.00 - $43.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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 Diego,CA.

Application Deadline

This position is anticipated to close on Sep 16, 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 withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment 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 thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall 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 applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

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Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Industry

Business management consulting

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

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