Top 48 Associate scientist Jobs in Santa Monica Ca

QA Specialist - Cell Therapy
GTT, LLC —Santa Monica, CA
- $35 - $40 an hour
- Contract
- Bachelor of Science
- Office
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
13d
Research Associate I, Dou Lab
Cedars-Sinai —Tarzana, CA
- $25.00 - $30.46 an hour
- 8 hour shift
- Bachelor's degree
- Fair chance
- AI
14d
Clinical Research Associate I, Dou Lab
Cedars-Sinai —Los Angeles, CA
- $25.00 - $33.51 an hour
- 8 hour shift
- HIPAA
- High school diploma or GED
- Bachelor's degree
Research Associate I - Ajami Lab - Department of Neurology
Cedars-Sinai —Los Angeles, CA
- $25.00 - $30.46 an hour
- 8 hour shift
- Computer literacy
- Bachelor's degree
- Neurology
Research Associate II - Lownik Lab - Pathology
Cedars-Sinai —Los Angeles, CA
- $24.00 - $36.14 an hour
- 8 hour shift
- Mid-level
- Bachelor's degree
- Organizational skills
Research Associate II
stealth mode —Los Angeles, CA
- $75,000 - $95,000 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
4d
Research Associate I Susan Cheng Team, Heart Institute
Cedars-Sinai —Los Angeles, CA
- $25.00 - $30.46 an hour
- 8 hour shift
- Bachelor of Science
- Cleaning
- Fair chance
Associate Research Scientist, Evidence Generation
Precision Medicine Group —Los Angeles, CA
- $66,000 - $94,000 a year
- Online Application
- Remote
- Mid-level
- Master's degree
- Business development
Lab Technician, Sample Prep & LC-MS/MS
Dalton Bioanalytics —Los Angeles, CA
- $52,000 - $62,000 a year
- Part-time
- Mid-level
- Cleaning
- In-person
- 401(k)
- Life insurance
Quick Apply
4d
Precision Laboratory Technician – Microscope & Crystal Handling
RiboForge, Inc. —Los Angeles, CA
- $20 - $35 an hour
- Part-time
- Computer literacy
- Mid-level
- High school diploma or GED
- Paid training
- Health insurance
Quick Apply
3d
Research Associate III - Ajami Lab - Department of Neurology
Cedars-Sinai —Los Angeles, CA
- $54,579.20 - $92,788.80 a year
- 8 hour shift
- Microsoft Word
- Computer literacy
- Mid-level
Project Scientist - Ajami Lab - Department of Neurology
Cedars-Sinai —Los Angeles, CA
- $66,560 - $133,120 a year
- 8 hour shift
- Mid-level
- Doctor of Philosophy
- Neurology
Research Associate - Biosensing
Convergent Research —Pasadena, CA
- $65,000 - $95,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Project management
- Paid holidays
- Dental insurance
Project Scientist - Genetics Research Center - Lakhani Lab - Full-Time, On-Site
Cedars-Sinai —Los Angeles, CA
- $66,560 - $133,120 a year
- 8 hour shift
- Doctoral degree
- Mid-level
- Neurology
Associate Research Scientist, Evidence Generation
Precision AQ —Los Angeles, CA
- $66,000 - $94,000 a year
- Online Application
- Remote
- Mid-level
- Master's degree
- Business development
Quick Apply
Pharmaceutical Manufacturing Technician
Siemens Healthineers —Culver City, CA
- $46,040 - $63,305 a year
- Overtime
- Word processing
- Mid-level
- High school diploma or GED
- Paid training
- Disability insurance
Environmental Staff Scientist
Giles Engineering Associates, Inc. —Los Angeles, CA
- Email
- Clean driving record
- Mid-level
- Office
Temporary - Senior Associate, QC Stability and Reference
ImmunityBio —Culver City, CA
- $35.50 - $39.00 an hour
- Full-time
- Microsoft Excel
- Mid-level
- Bachelor's degree
- AD&D insurance
- Disability insurance
Project Scientist - Genetics Research Center - Khokha Lab - Full-Time
Cedars-Sinai —Los Angeles, CA
- $66,560 - $133,120 a year
- 8 hour shift
- Doctoral degree
- Pediatrics
- Fair chance
1d
Project Scientist Position
UCLA —Los Angeles, CA
- $96,900 - $209,000 a year
- Online Application
- Psychiatry
- University
- Doctor of Philosophy

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QA Specialist - Cell Therapy

GTT, LLC -
Santa Monica, CA

Quick Apply

Job Details

Contract
$35 - $40 an hour
13 days ago

Benefits

Health insurance
Dental insurance
401(k)
Vision insurance

Qualifications

Biology
Investigations regulatory compliance
Bachelor of Science
Preventive action implementation
Technical writing experience within manufacturing
Production deviation management
Good documentation practices (GDP)
Quality control preventive actions
Corrective and preventive actions (CAPA)
GMP
Change management
Manufacturing facility experience
Quality assurance experience within pharmaceutical industry
Compliance documentation
Regulatory/legal compliance standards in production
Cleanroom experience
Chemistry
Product quality assurance
Production batch record review
Quality control records management
Pharmaceutical manufacturing facility experience

Full Job Description

QA Specialist - Cell Therapy

Location: Santa Monica, CA

Onsite Flexibility: Onsite

Contract Details

Position Type: Contract

Contract Duration: 8 months (possible extension)

Pay Rate: $35.00–$40.00 / Hour (USD)

Shift / Schedule: 9 AM – 5 PM, Sunday–Thursday OR Monday–Friday (possible weekend work)

Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Job Summary

This role provides Quality Assurance support to an assigned area. Typically, a graduate or equivalent, this is a non-supervisory position that provides technical advice in key areas of processes and procedures. The role holder impacts directly on the value stream by ensuring efficient processes and procedures are maintained within the boundaries of regulatory compliance for relevant GxP.

At the client's Oncology R&D division, the team follows the science to explore and innovate, working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. The organization has the potential to grow its pipeline and positively impact the lives of billions of patients around the world, built around a passion for science and now fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.

The Specialist, Quality ensures compliance with the quality system's procedures and assessments. This unique role is accountable for routine Quality Assurance responsibilities related to the production and disposition of products manufactured and tested on behalf of the client. This role is based in Tarzana, CA, and reports to the Manager, QA.

Key Responsibilities

Provide quality assurance support across technical operations functions (i.e., Manufacturing, Facilities & Engineering, Supply Chain, Quality Control, Analytical Development, Product Development/Manufacturing Sciences & Technology) within the organization to ensure compliance with the quality manual and maintain collaborative quality relationships.

Lead deviations and laboratory investigations related to GMP manufacturing and analytical testing, respectively, with cross-functional owners. Determine corrective/preventative actions (CAPA) and Verification of Effectiveness (VoE) and drive on-time implementation and closure.

Work with appropriate partners to manage change controls in a phase-appropriate manner for clinical stage products that support quality risk management (i.e., New Product Introduction, New Facility, & Manufacturing Process Change Controls).

Provide ILT training for annual GMP/GDP, Quality Manual, Quality Risk Management, Deviation/CAPA, and Change Control.

Work with QA doc control to ensure accurate issuance of batch record documentation (i.e., lot/media batch records and in-process/QC/final product labels) to manufacturing.

Review routine manufacturing batch documentation and quality control data for in-process and finished products to support disposition and lot closure.

Perform approval of equipment alarm acknowledgements, equipment activation, and PM/Calibration schedules in computerized asset and alarm management system(s).

Review routine material release documentation for the quality release of raw materials used for manufacturing and quality control testing.

Required Skills

Knowledge of and ability to apply GMP in conformance with US standards.

Proficient in cGMP regulations, quality systems, and regulatory requirements.

Experience writing, evaluating, and closing investigations, CAPAs, and change control.

Ability to adapt best practices for stage-appropriate products.

Education Requirements

MA/MS in Biology, Chemistry, Microbiology, Engineering, or a related field is required, OR a BA/BS with 2+ years, an Associate's degree with 4+ years, or a High School diploma with 5+ years of Quality Assurance or GMP experience.

Required Experience

2–4 years of Cell Therapy experience.

Work Environment / Physical Requirements

In-person working environment; on average, a minimum of three days per week from the office.

Possible weekend work depending on schedule assignment (Sunday–Thursday OR Monday–Friday schedule).

Important Notes

Interview Process: 2 rounds — 1st Teams Interview (30 minutes), 2nd Teams Interview (30 minutes).

Candidates must have direct QA responsibilities; Quality Control (QC) experience is not equivalent to the QA experience required for this role.

Role requires hands-on experience with batch record review, batch disposition, deviation management (from a QA reviewer perspective), change controls, and GMP documentation review.

Product complaint experience alone is not sufficient; the role requires manufacturing QA experience supporting batch review and product disposition.

Candidates should be prepared to explain in detail: how they handled deviations, how they manage batch record reviews, and what they look for during on-the-floor support.

The Specialist position is expected to be filled by someone with approximately 2–3 years of directly relevant QA experience who can contribute with minimal training.

Benefits

Medical, Vision, and Dental Insurance Plans

401k Retirement Fund

About the Client

This client is a leading biopharmaceutical and life sciences organization operating across strategic locations including the greater Los Angeles area and the Mid-Atlantic region. With a strong focus on Oncology R&D, the organization employs thousands of professionals — including quality assurance specialists, cell therapy scientists, R&D researchers, and manufacturing operations personnel — who collaborate to advance the next generation of life-changing medicines. The company's pipeline spans innovative cell therapy programs and other complex disease areas, reflecting a commitment to scientific excellence and regulatory rigor that positions it among the top-tier biopharma organizations in the industry.

About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number: 26-06896 Industry: Manufacturing & Operations

#LI-GTT #LI-Onsite

Pay: $35.00 - $40.00 per hour

Benefits:

401(k)
Dental insurance
Health insurance
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

associate scientist jobs in santa monica ca

QA Specialist - Cell Therapy

Research Associate I, Dou Lab

Clinical Research Associate I, Dou Lab

Research Associate I - Ajami Lab - Department of Neurology

Research Associate II - Lownik Lab - Pathology

Research Associate II

Research Associate I Susan Cheng Team, Heart Institute

Associate Research Scientist, Evidence Generation

Lab Technician, Sample Prep & LC-MS/MS

Precision Laboratory Technician – Microscope & Crystal Handling

Research Associate III - Ajami Lab - Department of Neurology

Project Scientist - Ajami Lab - Department of Neurology

Research Associate - Biosensing

Project Scientist - Genetics Research Center - Lakhani Lab - Full-Time, On-Site

Associate Research Scientist, Evidence Generation

Pharmaceutical Manufacturing Technician

Environmental Staff Scientist

Temporary - Senior Associate, QC Stability and Reference

Project Scientist - Genetics Research Center - Khokha Lab - Full-Time

Project Scientist Position

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