Top 1917 Program analyst Jobs in Pasadena, Ca

Quality Control Analyst
stealth mode —Los Angeles, CA
- $78,000 - $100,000 a year
- Full-time
- Mid-level
- 3 years
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
2d
Contract Instructional Designer/Trainer - Oracle Fusion HCM and ERP Systems
McCullough Management LLC —Long Beach, CA
- $50 - $75 an hour
- Urgently hiring
- Hybrid work
- Background check
- School experience
- Oracle
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Program Analyst SME - TS/SCI w/ Poly
General Dynamics Information Technology —El Segundo, CA
- $170,000 - $230,000 a year
- Bachelor of Science
- 11+ years
- Travel
- Paid time off
- 401(k) matching
Epic Interface Analyst
Elevance Health —Cerritos, CA
- $129,272 - $202,722 a year
- Contract
- Hybrid work
- Computer Science
- Bachelor of Science
- Office
- Employee stock purchase plan
- Paid holidays
12d
Chart Analyst - SCH
SCHARP —Los Angeles, CA
- $87,360 a year
- Mid-level
Quick Apply
Project Schedule Analyst III
APR Consulting Inc —Pasadena, CA
- $40 - $63 an hour
- 8 hour shift
- Office
- Master's degree
- Bachelor's degree
- Paid holidays
- Health insurance
Quick Apply
Sr. Program Analyst
General Dynamics Information Technology —California
- $93,662 - $103,500 a year
- Hybrid work
- 5 years
- Bachelor of Science
- Bachelor's degree
- Paid holidays
- 401(k) matching
Project Schedule Analyst IV
APR Consulting Inc —Pasadena, CA
- $49 - $80 an hour
- 8 hour shift
- Microsoft Excel
- 5 years
- Office
- Paid holidays
- Health insurance
Quick Apply
MSP Help Desk Engineer- Tier II
AllSafe IT —Pasadena, CA
- $30 - $36 an hour
- 8 hour shift
- Background check
- Azure
- Mid-level
- Paid holidays
- Health insurance
5d
Treasury Analyst
Parsons —Pasadena, CA
- $26.59 - $46.54 an hour
- Hybrid work
- Mid-level
- Office
- Finance
- Wellness program
- Paid holidays
Health Program Analyst I, Court Pre-Release
Heluna Health —Los Angeles, CA
- $5,943.91 - $8,575.40 a month
- Hybrid work
- Writing skills
- Mid-level
- Office
Resource Analyst II
JPL/NASA —Pasadena, CA
- $89,440 - $104,208 a year
- Full-time
- Microsoft Excel
- Research
- Mid-level
- Dental insurance
- Paid time off
Program Analyst (Public Records Specialist)
The State Bar of California —Los Angeles, CA
- $92,960 - $123,943 a year
- Full-time
- Hybrid work
- Word processing
- Writing skills
- Mid-level
Quick Apply
Compliance Analyst
UCLA Health —Los Angeles, CA
- $86,400 - $184,800 a year
- Research
- Mid-level
- 3 years
ANALYST I
CA Science Center —Los Angeles County, CA
- $3,861 - $6,276 a month
- Online Application
- Office
- Bachelor's degree
- Continuous improvement
DATA ANALYST-WORK FROM HOME
Qureos Inc —Los Angeles, CA
- $45 - $55 an hour
- Full-time
- Remote
- Computer Science
- Mid-level
- SQL
- Paid holidays
- Health insurance
7d
HEALTH PROGRAM ANALYST I/EMERGENCY APPOINTMENTS HOMELESSNESS
Los Angeles County Department of Human Resources —Los Angeles County, CA
- $87,520.32 - $117,941.52 a year
- Multiple hires
- Master's degree
- Analysis skills
- Bachelor's degree
Analyst, HMIS
Los Angeles Homeless Services Authority —Los Angeles, CA
- $70,304.00 - $92,398.47 a year
- Full-time
- Hybrid work
- Computer science
- Computer Science
- Bachelor of Science
- Paid holidays
- Disability insurance
1d
LICENSING PROGRAM ANALYST
Department of Social Services —Los Angeles County, CA
- $3,938 - $7,351 a month
- Full-time
- Hybrid work
- Writing skills
- Mid-level
- Office
- Paid holidays
- Health insurance
10d
Project Resource Analyst II
JPL/NASA —Pasadena, CA
- $89,440 - $104,208 a year
- Full-time
- Microsoft Excel
- Mid-level
- Office
- Dental insurance
- Paid time off

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program analyst jobs near pasadena, ca

Quality Control Analyst

stealth mode -
Los Angeles, CA

Quick Apply

Job Details

Full-time
$78,000 - $100,000 a year
2 days ago

Benefits

Health insurance
Dental insurance
401(k)
Vision insurance

Qualifications

Research design
Immunological assays
Design of experiments
ICH guidelines
Pharmaceutical analysis

Full Job Description

Role Description

We are a stealth-mode life sciences startup seeking a hands-on Quality Control Analyst to help build and advance our cell therapy manufacturing and quality control capabilities. This is a unique opportunity to contribute to the development of analytical methods, and quality systems that that will support our programs from early development through Phase 2 clinical studies and beyond.

In this highly collaborative role, you will contribute to process development, quality science, analytical development, and clinical translation, You will help develop and execute analytical testing strategies, establish scalable QC processes, and generate high-quality data that ensure product quality and process control throughout the manufacturing lifecycle. Working closely with Process Development, Bioanalytical, Quality Assurance, and external manufacturing partners, you will play a critical role in advancing innovative cell therapies toward the clinic.

This position is ideal for a scientist who enjoys hands-on laboratory work, solving complex technical challenges, and building scalable processes in a fast-paced startup environment. If you're energized by high-impact science at the intersection of biology, engineering, and clinical translation, and are excited to help build something from the ground up, we’d love to hear from you!

Key Responsibilities

QC Method Development & Qualification

Serve as a key in-lab contributor for qualifying analytical methods that support GMP manufacturing and clinical lot release.
Execute and support the design of well-controlled method development, optimization, and qualification/validation studies for potency, purity, identity, and safety attributes.
Qualify critical process analytics and release assays, including cell-based potency assays, flow cytometry panels, ELISA, qPCR, and imaging-based analyses relevant to ocular cell therapy products.
Author and review method protocols, validation reports, SOPs, specifications, and Certificates of Analysis (CoAs) in compliance with GMP documentation standards.
Maintain accurate and detailed records of all experimental plans, raw data, and analytical documentation.

QC Testing, Lot Release & Stability

Perform and/or oversee in-process, release, and stability testing of clinical-phase materials manufactured internally and through external partners.
Review and approve QC data packages and lot release documentation for clinical manufacturing programs.
Design and manage stability studies, including tracking, trending, and reporting to inform shelf-life strategy and regulatory submissions.
Identify out-of-trend (OOT) or out-of-specification (OOS) results; lead investigations including root cause analysis and CAPA development.

Analytics, Data Integrity & Reporting

Apply statistical tools and data analytics to evaluate method performance, trending, and process control data across manufacturing campaigns.
Author and contribute to CMC sections of regulatory submissions, including analytical methods, specifications, and QC data summaries.
Ensure QC data systems align with applicable data integrity requirements, including 21 CFR Part 11 expectations.
Collaborate with external CMOs and contract testing laboratories; represent QC in technical meetings, conduct method transfers, and perform on-site oversight visits as needed.

Qualifications:

Master’s or Bachelor’s degree in cell biology, biochemistry, analytical chemistry, pharmaceutical sciences, or a related scientific discipline
Minimum 3 years of hands-on experience in analytical method development and qualification for cell therapy, biologics, or gene therapy products.
Proficiency with assay platforms relevant to cell therapy QC; flow cytometry, cell-based potency assays, qPCR, ELISA, microscopy, and/or imaging analysis.
Demonstrated ability to design experiments, analyze complex datasets, and translate findings into actionable QC decisions.
Working knowledge of ICH guidelines and FDA/EMA expectations for advanced therapy medicinal products.
Ability to work independently while collaborating effectively across scientific and technical teams

Preferred Experience or Qualifications:

3+ years of biotech or pharmaceutical experience, with a strong preference for cell therapy or biologics manufacturing environments.
Experience in ocular biologics or ophthalmic cell therapy programs.
Experience developing or executing QC programs for iPSC-derived or primary cell therapy products.
Familiarity with GMP documentation practices, including SOPs, batch records, specifications and deviation/CAPA reporting.
Familiarity with automated imaging workflows or high-content analysis platforms for cell characterization.
Experience applying Design of Experiments (DoE) methodology to method optimization or process analytics.
Experience with tech transfer of analytical methods from research-grade to GMP-grade environments.
Proficiency with statistical software (e.g. JMP, Minitab) for QC data trending and method validation analysis.
Familiarity with electronic quality management systems (e.g. Veeva, MasterControl) and 21 CFR Part 11 compliance.

Why Join Us

As an early member of our team, you will have the opportunity to directly influence the development of innovative cell therapy technologies and help establish the quality foundation of a growing biotechnology company. Your work will play a critical role in advancing programs toward clinical milestones while collaborating with a team of scientists and innovators committed to making a meaningful impact for patients.

The annual base salary we expect to pay is $78,000-$100,000. Individual pay decision depends on various factors such as responsibility of role, job duties/requirements, and relevant experience and skills.

We are an equal opportunity employer.

We do not discriminate on the basis of race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any characteristic protected under applicable law.

Pay: $78,000.00 - $100,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

program analyst jobs in pasadena, ca

Quality Control Analyst

Contract Instructional Designer/Trainer - Oracle Fusion HCM and ERP Systems

Program Analyst SME - TS/SCI w/ Poly

Epic Interface Analyst

Chart Analyst - SCH

Project Schedule Analyst III

Sr. Program Analyst

Project Schedule Analyst IV

MSP Help Desk Engineer- Tier II

Treasury Analyst

Health Program Analyst I, Court Pre-Release

Resource Analyst II

Program Analyst (Public Records Specialist)

Compliance Analyst

ANALYST I

DATA ANALYST-WORK FROM HOME

HEALTH PROGRAM ANALYST I/EMERGENCY APPOINTMENTS HOMELESSNESS

Analyst, HMIS

LICENSING PROGRAM ANALYST

Project Resource Analyst II

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