Top 9 Quality control lab technician Jobs in El Cajon, Ca

QC Technologist III
Werfen —San Diego, CA
- $34 - $39 an hour
- Temporary
- ERP systems
- Data analysis skills
- Maintenance
Quality Assurance - QA Lab Technician 1st shift
Chromalloy —San Diego, CA
- $21.07 - $37.48 an hour
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Wellness program
- Paid holidays
Quick Apply
11d
Packaging Quality Lab Manager
Monster Energy —San Diego, CA
- $100,500 - $134,000 a year
- SharePoint
- Manufacturing
- Senior level
Quick Apply
5d
QC Associate I
Software Technology Inc —San Diego, CA
- 8 hour shift
- Microsoft Word
- Computer literacy
- Bachelor of Science
Quick Apply
Quality Control Associate
Software Technology Inc —San Diego, CA
- Word processing
- Computer literacy
- Bachelor of Science
Quick Apply
QC Associate
Software Technology Inc —San Diego, CA
- Computer literacy
- Bachelor of Science
- Writing skills
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
QC Associate (Flow Cytometry and Tissue Culture)
Software Technology Inc —San Diego, CA
- Computer literacy
- Bachelor of Science
- Writing skills
Quick Apply
Quality Control Associate I, Flow Cytometry (PM Shift)
Revvity —San Diego, CA
- $19.00 - $26.50 an hour
- Full-time
- Data analysis skills
- High school diploma or GED
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance

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QC Technologist III

Werfen -
San Diego, CA

Apply Now

Job Details

Temporary
$34 - $39 an hour

Qualifications

ISO standards
Maintenance
High school diploma or GED
Quality audits
FDA regulations

Full Job Description

Job Information

Number

ICIMS-2026-10510

Job function

Manufacturing

Job type

Temporary

Location

Werfen - San Diego - WBH - 6260 Sequence Drive San Diego, California 92121 United States

Country

United States

Shift

1st

About the Position

Introduction

Werfen

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.

Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

Overview

Job Summary:

The QC Lab Technologist III is responsible for the execution of a broad range of bench test procedures used in raw material qualification, the testing of finished goods prior to release, the investigations of product performance, and for conducting routine validation studies, as well as assisting with routine maintenance of the Quality Control (QC) laboratory. The QC Lab Technologist III works with cross-functional teams to resolve product performance issues and maintenance of QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards. Additionally, QC Lab Technologist III supports investigations and performs in depth analysis of the trending of finished product testing data. The QC Lab Technologist III manages basic projects independently of management.

The base hourly range for this role is currently $34.00/hr. to $39.00/hr. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs.

Responsibilities

Key Accountabilities

Essential Functions:

Perform testing of finished goods per relevant SOP.
Perform testing for product validation and process validation on new and existing products and demonstrate the ability to understand the validation. Assist with the development of validation, including feedback on testing requirements and turn around time.
Maintain proper laboratory housekeeping and supply levels in the QC laboratory, including submission of purchase requisitions and inventory adjustments and exhibiting knowledge of product usage based on planned production to ensure safety stock and continued supply.
Document all test results and maintain product release records (including electronic records).
Maintain product testing database and trending associated with product specifications as specified in laboratory SOPs.
As required, coordinate and assist with investigations and resolution of complaints, non-conforming material and product performance issues, including recommending and orga- nizing test protocols for investigation.
Perform testing of biological raw materials, including range generation or characterization. Organize and complete associated paperwork. As required, manage concentration selec- tion and release. Organize and schedule basic testing requirements with minimal supervi- sion.
Perform testing and prepare reports as required, such as environmental monitoring reports or investigation of out-of-specification results, as required.
Responsible for tracking and analyzing trends related to release testing. Ability to use analysis of trends to provide input on product issues and results.
Perform testing and assist with preparation of reports for various special projects as dee- med necessary by technical review team.
Responsible as a subject matter expertise in at least one product line.
Submit complex change orders to update procedures as required.
As required, interact independently with cross-functional teams to obtain information on testing, provide feedback and information, and demonstrate critical evaluation of testing requests. Assist the cross-functional team to investigate and resolve issues.
Exhibit ability to manage multiple projects/responsibilities with little supervision.
Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes.
Other duties as assigned.

Internal Networking/Key Relationships:

Quality Release, Research and Development, Quality Engineering, and Manufacturing Persononel.

Qualifications

Minimum Knowledge & Experience Required for the Position:

High school diploma required, Bachelor’s degree in Science or equivalent experience pre- ferred.
Work Experience:
- Without Related degree: A minimum of five (5) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required
- With Related degree: A minimum of four (4) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required
- Previous experience within a regulated medical device manufacturing or In-Vitro Diagnostic Device (IVDD) strongly preferred.
Thorough understanding of Good Laboratory Practices (GLP) required.
Practical experience with laboratory controls, internal audits, and lab training/maintenance.
Phlebotomy certification a plus.
Knowledge of FDA-GMP/QSR and ISO standards for quality.

Skills & Capabilities:

Technical Skills:

Excellent written and verbal communication skills.
Ability to work independently and as part of a team.
Proficiency with common laboratory techniques, such as pipetting and use of balances.
Proficiency with Microsoft Office suite.
Proficiency with Large Enterprise Resources Planning (ERP).
Must occasionally lift up to 25 lbs.

Competencies:

Attention to Detail: Advanced ability to pay close attention to detail is required
Accuracy: Work is accurate and completeness of records
Outstanding Performance Standards: Demonstrated ability to meet department goals
Communication: Good written and verbal communication skills
Discretion: Acts Honest, Loyal, trustworthy
Multi-Tasking: Advanced ability to Juggle Priorities, and support changing busi- ness needs. Exhibit ability to manage multiple projects/responsibilities with little supervi- sion.
Collaboration: Advanced ability to actively develop a network to bring best solutions to the team or customer
Independence: self-motivated-works under minimal supervision
Professionalism: Must demonstrate professionalism during all interactions within com- pany, customer and third parties
Takes Initiative: Serves as a role model for “Quality First” by continuously improving on what matters most to customers
Problem Solving: Promptly and effectively handles advanced issues and problems with minimal supervision or management.

Travel Requirements:

If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.

Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact [email protected] for assistance.

We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.

www.werfen.com

Apply Now

Refine Your Search

quality control lab technician jobs in el cajon, ca

QC Technologist III

Quality Assurance - QA Lab Technician 1st shift

Packaging Quality Lab Manager

QC Associate I

Quality Control Associate

QC Associate

QC Associate I [Must have ELISA or CBA Exp]

QC Associate (Flow Cytometry and Tissue Culture)

Quality Control Associate I, Flow Cytometry (PM Shift)

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