Top 1 Quality control analyst Jobs in Fallbrook, Ca

QC Analyst
Novartis —Carlsbad, CA
- $70,000 - $130,000 a year
- 12 hour shift
- Data analysis skills
- Mid-level
- Bachelor's degree
- Health insurance
- 401(k) matching

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QC Analyst

Novartis -
Carlsbad, CA

Apply Now

Job Details

Full-time
$70,000 - $130,000 a year

Benefits

Health insurance
401(k) matching

Qualifications

Data integrity assurance
Data quality checks
Instrumentation troubleshooting
Laboratory equipment routine checks
Pharmaceutical regulatory compliance
Preventive action implementation
High-performance liquid chromatographs
Data analysis skills
Production deviation management
Equipment troubleshooting
Corrective and preventive actions (CAPA)
GMP
Laboratory equipment calibration
Data integrity and documentation
Bachelor's degree
Pharmaceutical company experience
Data quality monitoring
Pharmaceutical analysis
Compliance documentation
Laboratory preventive maintenance
Quality control experience within pharmaceutical industry
Cross-functional collaboration
Cross-functional communication
Pharmaceutical manufacturing facility experience
Laboratory compliance and regulatory documentation

Full Job Description

Summary

Imagine being part of a team that helps ensure every product reaching patients meets the highest standards of quality, safety, and compliance. As a QC Analyst, you will play a critical role in generating reliable analytical data that supports product release, stability programs, and continuous quality improvement. Working in a collaborative laboratory environment, you’ll apply your scientific expertise to solve complex challenges, strengthen quality operations, and help deliver medicines that make a meaningful difference for patients.

About the Role

#LI-Onsite

Location: Carlsbad, CA

Relocation Support: This role is based in Carlsbad, CA. Novartis is unable to offer relocation support: please only apply if accessible.

Shift: 4x3 12-hour shift Sunday to Tuesday, 8:00AM - 8:00PM / alternating Wednesdays, Thursday - Saturday 8:00AM - 8:00PM, (Wednesday alternating every other week). Periodic mandatory overtime may be necessary to ensure process continuity and completion.

Key Responsibilities

Perform analytical testing of products, materials, and stability samples following approved laboratory procedures.

Review and approve analytical data to support product release and ensure data integrity compliance.

Conduct High-Performance Liquid Chromatography and Ultra Performance Liquid Chromatography testing and analysis.

Support stability programs through protocol preparation, testing, evaluations, and technical reporting.

Investigate deviations, support corrective and preventive actions, and contribute to quality trend analysis.

Perform equipment calibration, maintenance, and qualification activities to ensure laboratory readiness.

Execute microbiological testing, environmental monitoring, and utility sampling to support quality operations.

Maintain accurate Good Manufacturing Practice documentation and ensure compliance with laboratory quality standards.

Essential Requirements

Bachelor's degree in chemistry, Biochemistry, Microbiology, or related scientific discipline.

Experience performing analytical testing in a United States Food and Drug Administration regulated pharmaceutical manufacturing environment.

Knowledge of Good Manufacturing Practice requirements and laboratory compliance standards.

Experience with High-Performance Liquid Chromatography and related analytical laboratory techniques.

Demonstrated experience investigating deviations and supporting corrective and preventive action activities.

Understanding of data integrity principles and compliant laboratory documentation practices.

Experience calibrating, maintaining, and troubleshooting laboratory equipment and instrumentation.

Strong communication, problem-solving, and cross-functional collaboration skills.

Desirable Requirements

Experience performing endotoxin testing, product release testing, or related analytical quality control assays.

Experience with or knowledge of Empower software

The salary for this position is expected to range between $70,000 and $130,000 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click here.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Accessibility & Reasonable Accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Division

Operations

Business Unit

Production / Manufacturing

Location

USA

State

California

Site

Carlsbad

Company / Legal Entity

U469 (FCRS = US469) AAA USA Inc.

Functional Area

Quality

Job Type

Full time

Employment Type

Regular

Shift Work

Apply Now

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