Top 15 quality control associate Jobs in camp pendleton, ca

Quality Control Associate I
Genentech —Oceanside, CA
- $52,600 - $84,000 a year
- Online Application
- Ability to walk for extended periods
- Mid-level
- 3 years
3d
Quality Control Associate II
Genentech —Oceanside, CA
- $66,200 - $110,000 a year
- Online Application
- Google Workspace
- Ability to walk for extended periods
- 5 years
- On-the-job training
2d
Research Associate II, Analytical Development & Quality Control (ADQC)
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $71,219 - $90,448 a year
- Hybrid work
- Bachelor of Science
- Mid-level
- Bachelor's degree
Quick Apply
QC Sr. Associate I (QC Lab Support LIMS Specialist)
Genentech —Oceanside, CA
- $90,100 - $167,300 a year
- Online Application
- 3 years
- Bachelor's degree
- Mentoring
Quality Control Associate I / II
Pharmaron —Carlsbad, CA
- $25 - $33 an hour
- Online Application
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
- AD&D insurance
- Disability insurance
Quick Apply
8d
Senior Associate, Quality Control, Raw Materials
Artiva Biotherapeutics —San Diego, CA
- $96,000 - $110,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
Quick Apply
Quality Assurance Associate
San Diego Sign Company/ d.b.a WS Display —Carlsbad, CA
- $20 an hour
- Full-time
- Ability to walk for extended periods
- Databases
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
4d
Clinical - QA Associate, Clinical Studies
Medvacon Life Sciences, LLC —San Diego, CA
- $33 an hour
- 8 hour shift
- Mid-level
- Math
- Associate's degree
9d
QC Associate I
Software Technology Inc —San Diego, CA
- 8 hour shift
- Microsoft Word
- Computer literacy
- Bachelor of Science
Quick Apply
QC Associate I [Must have ELISA or CBA Exp]
Software Technology Inc —San Diego, CA
- 8 hour shift
- Word processing
- Computer literacy
- Bachelor of Science
Quick Apply

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Perform incoming QA of machined parts to meet GD&T requirements of engineering drawings using calibrated metrology tools and a state-of-the-art Keyence Optical…
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Quality Control Associate II
Genentech —Oceanside, CA
This role requires technical proficiency in chemical assays and compendial testing, balancing hands-on routine and non-routine analysis with significant…
$66,200 - $110,000 a year
2d

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Quality Control Associate I

Genentech -
Oceanside, CA

Apply Now

Job Details

Full-time
$52,600 - $84,000 a year
3 days ago

Qualifications

Raw material quality management
Bachelor's degree
Pharmaceutical company experience
Quality control within pharmaceutical industry
Pharmaceutical manufacturing facility experience

Full Job Description

The Position

We are seeking a QC Associate to support direct material (raw material) testing. As a Quality Control Associate I, you will be responsible for compendial method testing, direct material (raw material), reagent preparation, and sample management for biopharmaceutical products. Additional responsibilities include equipment management and maintenance, and laboratory duties.

The Opportunity

Compliance and Quality System Adherence: Apply advanced knowledge of GMP, GDP, and Data Integrity ALCOA principles daily. Follow established safety and environmental guidelines and maintain the laboratory in an inspection-ready state (e.g.,5S implementation).
Core Compendial Testing: Execute and document routine and non-routine compendial testing, including pH, osmolality, Karl Fischer, basic wet chemistry, and other general techniques according to established procedures.
Chemical Assay Execution: Perform specialized chemical assays and analysis, collect and process data, and ensure results are reported accurately and on time.
Equipment Maintenance and Readiness: Perform daily and periodic laboratory equipment maintenance, including calibration and standardization of equipment, to ensure continuous readiness and compliance.
Technical Support and Troubleshooting: Perform basic troubleshooting of chemical assays and provide initial support for instrument issues to minimize downtime.
Materials and Inventory Management: Perform sample management and aliquoting. Manage laboratory supplies by performing inventory checks and stocking supplies as needed (e.g., preparing reagents).
Investigation and Data Review: Assist in data trending and data review for conformance to specifications. Assist with or lead laboratory investigations OOS/OOT with appropriate oversight.
Training and Cross-Functional Liaison: Train others in basic to complex laboratory and troubleshooting techniques. Serve as a liaison for daily activities and special projects within QC or cross-functionally.
Independent Execution: Demonstrate the ability to work independently with little supervision and provide support for the execution of studies and protocols as needed

Who you are

You possess a Bachelor’s degree in Chemistry, Biochemistry, or a related scientific discipline with 3-4 years of experience in pharmaceutical/biotech QC labs, including hands-on raw material testing under cGMP.

Knowledge, Skills, and Abilities

Foundational Analytical Skills: Basic knowledge in Chromatography and chemical testing assays. Includes basic equipment troubleshooting techniques and proficiency in all necessary wet chemistry methods.
GMP Execution & Compliance: Experience working in a GMP environment with the ability to read and follow Standard Operating Procedures precisely. Possesses knowledge of laboratory safety procedures and basic experience supporting quality events.
Data & Systems Proficiency: Proficiency with laboratory electronic systems, including LIMS and Microsoft Office. Working knowledge of Empower or GSMP software is preferred.
Agile Teamwork & Organization: Demonstrates excellent organizational skills and the ability to be agile and work independently in a fast-paced environment. Experience working on group projects and proficient in time management with oversight.
Quality Mindset & Communication: Excellent interpersonal, written, and verbal communication skills. Possesses a continuous improvement mindset and basic experience supporting audit or inspection activities.
Work in office and laboratory environments.

Physical & Work Environment Requirements

Must be able to stand, walk, and use laboratory equipment for extended periods.
Ability to lift up to 35 lbs and wear necessary personal protective equipment (PPE).
Work is performed in a cGMP-regulated manufacturing facility.
Work with analytical instruments that may involve exposure to hazardous chemicals (corrosive, toxic, flammable, etc)

Travel may be up to 25% during start-up laboratory activities. No more than 10% travel expected during routine operations.

Relocation benefits are not available for this posting

The expected salary range for this position based on the primary location of California is $52,600 - $84,000 Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

Benefits

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Apply Now

Refine Your Search

quality control associate jobs in camp pendleton, ca

Quality Control Associate I

Quality Control Associate II

Research Associate II, Analytical Development & Quality Control (ADQC)

QC Sr. Associate I (QC Lab Support LIMS Specialist)

Quality Control Associate I / II

Senior Associate, Quality Control, Raw Materials

Quality Assurance Associate

Clinical - QA Associate, Clinical Studies

QC Associate I

QC Associate I [Must have ELISA or CBA Exp]

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