Sr Associate Immunology Scientist

ACTalent; Thousand Oaks (CA); On-site; USD 31,000 - 44,000; Full time

Benefits offered by this job

Medical, dental & vision benefits

401(k) Retirement Plan

Paid time off (PTO)

Job summary

Actalent is seeking a Senior Associate, Bioanalytical Sciences for a 100% onsite role in Thousand Oaks, CA. You will plan and execute immunoassays such as ELISA within a regulated GxP environment, document results meticulously, and collaborate across an interdisciplinary team to drive bioanalytical studies forward.

The role emphasizes strong pipetting skills, data analysis, and adherence to GMP/GLP practices, with standard 9-to-5 hours in a lab setting.

Qualifications

• Requires a Bachelor's degree in Life Sciences or closely related field.
• At least 3 years of lab-based research experience under GxP regulations.
• Hands-on experience with ELISA and other immunoassays.
• Strong pipetting technique and ability to handle biological samples.
• Regulated bioanalysis experience with focus on quality and compliance.
• Proficient in Good Documentation Practices and record-keeping.

Responsibilities

• Plan, perform, and optimize immunoassays (ELISA and others) in a GMP/GLP lab.
• Participate in method development and validation activities.
• Prepare and analyze biological samples with sensitive pipetting.
• Analyze and interpret experimental data; propose solutions to problems.
• Document procedures and results following GxP; maintain electronic records.
• Operate specialized lab equipment and data collection systems.
• Communicate findings via reports, records, and presentations.
• Collaborate with colleagues in a highly interactive R&D environment.
• Ensure compliance with GMP, GLP, and GxP regulations.

Skills

ELISA & immunoassays

Pipetting technique

Data analysis & interpretation

Good Documentation Practices

GxP compliance (GMP/GLP)

Verbal & written English communication

Team collaboration

Laboratory technique automation

Education

Bachelor's degree in Life Sciences

Tools

Automated liquid handling platforms

Job description

Job Title: Senior Associate, Bioanalytical Sciences

Job Description

This onsite, lab-based role offers the opportunity to contribute to cutting-edge bioanalytical research within a regulated GxP environment. As a Senior Associate in the Bioanalytical Sciences group, you will plan and execute immunoassays, organize and analyze data, and help solve technical problems related to regulated bioanalysis. You will work closely with a collaborative team, applying strong documentation practices, quality-focused thinking, and excellent pipetting skills to support bioanalytical studies.

Responsibilities

• Plan, perform, and optimize immunoassays, including ELISA and other relevant formats, in a regulated GxP laboratory environment.
• Participate in method development and validation activities to ensure robust and reliable bioanalytical assays.
• Prepare and analyze biological samples with strong pipetting technique and attention to detail.
• Organize, analyze, and interpret your own experimental data, drawing meaningful conclusions and proposing solutions to technical problems.
• Apply Good Documentation Practices to record experimental procedures, observations, and results accurately and comprehensively.
• Operate specialized laboratory equipment and use computer systems to collect, process, and manage experimental data.
• Communicate experimental findings clearly through written reports, electronic records, and verbal presentations.
• Collaborate effectively with colleagues in a highly interactive research and development environment, contributing to team goals and shared projects.
• Adhere to GMP, GLP, and broader GxP regulations in all laboratory activities, ensuring quality-focused and compliant bioanalysis.
• Support continuous improvement of laboratory workflows, documentation standards, and assay performance through proactive problem-solving.

Essential Skills

• Bachelor's degree in Life Sciences or a closely related discipline.
• Minimum of 3 years of laboratory-based research experience in academic or industrial settings under GxP regulations.
• Hands-on experience and knowledge in ELISA and other immunoassays.
• Strong pipetting technique and experience preparing and handling biological samples.
• Demonstrated regulated bioanalysis experience with a focus on quality and compliance.
• Proficiency in Good Documentation Practices and strong record-keeping skills.
• Ability to operate specialized laboratory equipment used in bioanalytical assays.
• Good computer skills for data collection, analysis, and documentation.
• Effective verbal and written English communication skills.
• Excellent interpersonal skills and ability to work in a collaborative team environment.

Additional Skills & Qualifications

• Experience working within GMP and GLP laboratory environments.
• Knowledge and experience in performing a range of immunoassays, especially ELISA.
• Experience with automation systems, such as automated liquid handling platforms.
• Strong organizational skills and the ability to manage multiple experiments and datasets simultaneously.
• Detail-oriented, creative, and highly motivated approach to scientific problem-solving.
• Ability to work effectively in a highly collaborative research and development environment.
• Quality-focused mindset with an emphasis on accuracy, reliability, and regulatory compliance.

Work Environment

This is a 100% onsite, lab-based position with a standard schedule of 9:00 a.m. to 5:00 p.m. You will work in a regulated GxP bioanalytical laboratory that follows GMP and GLP standards, using specialized equipment and computer systems to perform immunoassays such as ELISA and related techniques. The environment is highly collaborative, research- and development-focused, and emphasizes quality, documentation accuracy, and compliance. Laboratory attire appropriate for a GxP setting, including use of standard personal protective equipment, is required while performing experimental work.

Job Type & Location

This is a Contract position based out of Thousand Oaks, CA.

Pay And Benefits

The pay range for this position is $27.00 - $27.00/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)

Job Type & Location

This is a Contract position based out of Thousand Oaks, CA.

Application Deadline

This position is anticipated to close on Nov 13, 2026.

Workplace Type

This is a fully onsite position in Thousand Oaks,CA.

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 [e-mail] 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.