Top 889 Pharmaceutical Jobs in Manhattan Beach, 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
Research Technician, Automated Staining
Molecular Instruments —Los Angeles, CA
- $28 - $38 an hour
- Full-time
- No experience needed
- Mid-level
- Cleaning
- Health insurance
- Dental insurance
Quick Apply
10d
Pharmacy Clinical Systems Administrator
UCLA Health —Los Angeles, CA
- $39.93 - $69.93 an hour
- Monday to Friday
- System design
- Mid-level
- Bachelor's degree
Ambulatory Pharmacy Technician
UCLA Health —Los Angeles, CA
- $27.88 - $42.46 an hour
- Weekends as needed
- Ability to lift 50 pounds
- Ability to sit for extended periods
- Medical terminology
Quality Assurance Specialist
Cube Hub Inc —El Segundo, CA
- $40 - $43 an hour
- Weekends as needed
- Background check
- Microsoft Excel
- Pass drug screening
- Health insurance
- Dental insurance
Quick Apply
1d
Clinical Research Data Specialist I
USC —Los Angeles, CA
- $26.77 - $34.32 an hour
- Experience equivalent to degree accepted
- Associate's degree
- Medical terminology
Facilities Ops Specialist I
Kite Pharma —El Segundo, CA
- $86,275 - $111,650 a year
- Full-time
- Mid-level
- 3 years
- Databases
- Health insurance
- Dental insurance
Validation Engineer I
ImmunityBio —El Segundo, CA
- $88,200 - $98,000 a year
- Full-time
- Ability to lift 50 pounds
- Bachelor's degree
- Organizational skills
- AD&D insurance
- Disability insurance
Pharmaceutical Representative
Access Pharmaceutical —Beverly Hills, CA
- Organizational skills
- Leadership
- Communication skills
QC Lab Tech II
Kite Pharma —El Segundo, CA
- $55,930 - $72,380 a year
- Overtime
- OSHA
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
12d
Process Validation Specialist - Torrance
PolyPeptide US —Torrance, CA
- $80,000 - $100,000 a year
- Overtime
- Engineering
- Mid-level
- Analysis skills
Analyst I Business Operations
Kite Pharma —Santa Monica, CA
- $74,715 - $96,690 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Oracle
- Customer service
- Health insurance
- Dental insurance
3d
Laboratory Assistant I
Labcorp —Torrance, CA
- $17.81 - $26.12 an hour
- Overtime
- High school diploma or GED
- Fair chance
- 1 year
- Employee stock purchase plan
- Disability insurance
9d
Pharmaceutical Lab Technician
Siemens Healthineers —Culver City, CA
- $53,400 - $73,425 a year
- Overtime
- Customer service
- Word processing
- Computer literacy
- Paid training
- Disability insurance
Clinical Research Specialist I – Oncology & Clinical Research
Cedars-Sinai —Los Angeles, CA
- $31.75 - $53.98 an hour
- 8 hour shift
- Hybrid work
- Hospital
- HIPAA
- 3 years
Account Specialist, Anti Infectives - Torrance, CA
AbbVie —Torrance, CA
- $78,500 - $192,500 a year
- Full-time
- Remote
- Pass drug screening
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
Pharmaceutical Sales Specialist - R&I Primary Care - Long Beach, CA
AstraZeneca —Long Beach, CA
- Call employer
- Clean driving record
- Primary Care
- Driver's License
10h
Territory Rep – Pharmaceutical
Access Pharmaceutical —Glendale, CA
- Mid-level
- Communication skills
- Marketing
Clinical Scientist/Neuropsychological Rater
Irvine Clinical Research —Long Beach, CA
- $85,000 a year
- Full-time
- Master of Social Work
- Psychiatry
- English
- Dental insurance
- Paid time off
Quick Apply
Sr Quality Engineer I
Kite Pharma —El Segundo, CA
- $123,930 - $160,380 a year
- Full-time
- System design
- Master's degree
- High school diploma or GED
- Health insurance
- Dental insurance
12d

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Quality Control Analyst

stealth mode -
Los Angeles, CA

Quick Apply

Job Details

Full-time
$78,000 - $100,000 a year

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

pharmaceutical jobs in manhattan beach, ca

Quality Control Analyst

Research Technician, Automated Staining

Pharmacy Clinical Systems Administrator

Ambulatory Pharmacy Technician

Quality Assurance Specialist

Clinical Research Data Specialist I

Facilities Ops Specialist I

Validation Engineer I

Pharmaceutical Representative

QC Lab Tech II

Process Validation Specialist - Torrance

Analyst I Business Operations

Laboratory Assistant I

Pharmaceutical Lab Technician

Clinical Research Specialist I – Oncology & Clinical Research

Account Specialist, Anti Infectives - Torrance, CA

Pharmaceutical Sales Specialist - R&I Primary Care - Long Beach, CA

Territory Rep – Pharmaceutical

Clinical Scientist/Neuropsychological Rater

Sr Quality Engineer I

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