The QC Associate I will prioritize daily workload and work independently. · They will participate in the review of data, report results, and complete all required documentation and database entries.
Quick apply
The QC Associate I will prioritize daily workload and work independently. · They will participate in the review of data, report results, and complete all required documentation and database entries.
Quick apply
The QC Associate I will prioritize daily workload and work independently. · They will participate in the review of data, report results, and complete all required documentation and database entries.
Job Summary BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow ...
Job Summary BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow ...
$52K - $84K/yr
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.
$52K - $84K/yr
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.
Oceanside, CA · On-site
$52K - $84K/yr
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.
Oceanside, CA · On-site
$52K - $84K/yr
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.
Qualifications Education: BS/MS in Biology/Molecular Biology, biochemistry, chemistry or related discipline 2 to 5 years of industry experience with Functional analysis QC of molecular-biology-based ...
Qualifications Education: BS/MS in Biology/Molecular Biology, biochemistry, chemistry or related discipline 2 to 5 years of industry experience with Functional analysis QC of molecular-biology-based ...
San Diego, CA · On-site
$70K - $87K/yr
Position Summary The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor's manufacturing processes. This role ...
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San Diego, CA · On-site
$70K - $87K/yr
Position Summary The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor's manufacturing processes. This role ...
San Diego, CA · On-site
$70K - $87K/yr
Position Summary The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor's manufacturing processes. This role ...
San Diego, CA · On-site
$70K - $87K/yr
Position Summary The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor's manufacturing processes. This role ...
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
$70K - $87K/yr
Position Summary The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor's manufacturing processes. This role ...
$70K - $87K/yr
Position Summary The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor's manufacturing processes. This role ...
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Quick apply
San Diego, CA · On-site
$75K - $87K/yr
The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Job Title: QC Associate - Flow Cytometry Schedule: 9:00 AM - 5:30 PM Interview Type: In-person Requirement: Must have hands-on Flow Cytometry experience (data acquisition + analysis) Job Summary We ...
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Job Title: QC Associate - Flow Cytometry Schedule: 9:00 AM - 5:30 PM Interview Type: In-person Requirement: Must have hands-on Flow Cytometry experience (data acquisition + analysis) Job Summary We ...
Carlsbad, CA · On-site
$33 - $45/hr
The QC Associate may also support the QC department by means of executing the analysis of in-process, finished product, and stability test samples. QC personnel are responsible for compliance with QC ...
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Carlsbad, CA · On-site
$33 - $45/hr
The QC Associate may also support the QC department by means of executing the analysis of in-process, finished product, and stability test samples. QC personnel are responsible for compliance with QC ...
Carlsbad, CA · On-site
$33 - $45/hr
The QC Associate may also support the QC department by means of executing the analysis of in-process, finished product, and stability test samples. QC personnel are responsible for compliance with QC ...
Carlsbad, CA · On-site
$33 - $45/hr
The QC Associate may also support the QC department by means of executing the analysis of in-process, finished product, and stability test samples. QC personnel are responsible for compliance with QC ...
The QC Associate may also support the QC department by means of executing the analysis of in-process, finished product, and stability test samples. QC personnel are responsible for compliance with QC ...
The QC Associate may also support the QC department by means of executing the analysis of in-process, finished product, and stability test samples. QC personnel are responsible for compliance with QC ...
Oceanside, CA · On-site
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 ...
Oceanside, CA · On-site
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 ...
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 ...
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 ...
Job Summary BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow ...
Job Summary BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow ...
San Diego, CA · On-site
$40 - $60/hr
The Quality Control (QC) Associate I / II is responsible for performing analytical testing and laboratory activities that support stability, qualification/validation, and supporting release testing ...
San Diego, CA · On-site
$40 - $60/hr
The Quality Control (QC) Associate I / II is responsible for performing analytical testing and laboratory activities that support stability, qualification/validation, and supporting release testing ...
Job Summary QC Flow Associates focused on cell & tissue culture are highly motivated team members that will primarily be responsible for the preparation of primary cells and the culture of various ...
Job Summary QC Flow Associates focused on cell & tissue culture are highly motivated team members that will primarily be responsible for the preparation of primary cells and the culture of various ...
$12.14 - $14.69
3% of jobs
$14.69 - $17.24
12% of jobs
$19.50 is the 25th percentile. Wages below this are outliers.
$17.24 - $19.79
12% of jobs
$19.79 - $22.34
14% of jobs
$22.34 - $24.89
8% of jobs
The median wage is $25.53 / hr.
$24.89 - $27.45
6% of jobs
$27.45 - $30
7% of jobs
$32.23 is the 75th percentile. Wages above this are outliers.
$30 - $32.55
15% of jobs
$32.55 - $35.10
14% of jobs
$35.10 - $37.65
6% of jobs
$37.65 - $40.20
3% of jobs
$12
$26
$40
| Aspect | Quality Control Associate | Quality Assurance Technician |
|---|---|---|
| Certifications | Often requires GMP, ISO, or industry-specific quality certifications | Similar certifications, with focus on quality standards and compliance |
| Work Environment | Laboratory, manufacturing, or production settings | Laboratory, manufacturing, or quality compliance environments |
| Primary Focus | Inspecting products, testing samples, identifying defects | Developing and implementing quality systems, audits, and process improvements |
| Employer & Industry Usage | Manufacturing, pharmaceuticals, food production | Manufacturing, pharmaceuticals, food industry |
While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

Job Title: Spec 1, Quality Control
Location: San Diego California 92130
Duration:12 Months
JOB DESCRIPTION
TECHNICAL SKILLS
Must Have
Nice To Have
· Shift hours – 9-5:30pm
· Interviews video, phone or in person –in person
· Must haves on resume – hands-on Flow Cytometry experience, data acquisition and analysis included
· The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols. The QC Associate I will prioritize daily workload and work independently.
· They will participate in the review of data, report results, and complete all required documentation and database entries. QC Associate I will receive specific instructions and ongoing guidance regarding required tasks and expected results.
JOB RESPONSIBILITIE
· Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting.
· This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues
· Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures.
· Will prioritize daily workload and develop skills to work independentl
· Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures.
· Calibrate and maintain equipment. Report problems to QC Supervisor or Manager.
· Maintain logs and required documentation, as necessary.
· Prepare lab supplies, reagents, and assist with laboratory maintenance, as needed.
· Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment
· Participate in Environmental, Health & Safety programs.
· Address corrective actions whenever a hazard is identified
· Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.
· Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements.
· Participate in group or intra-department teams and projects as required.
· Participate in assigned cross-training.
· Perform other related duties and assignments, as required.
EDUCATION AND EXPERIENCE
· BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years related experience in a biotech lab environment.
· Experience in an industrial or research laboratory preferred.
· Flow Cytometry experience required
· Tissue Culture experience highly preferred.
KNOWLEDGE AND SKILLS
· Basic computer skills: MS Excel & Word.
· Knowledge of general laboratory safety
· Effective interpersonal, written and oral communication skills.
· Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs.
· Effective analytical and problem-solving skills.
Sourced by ZipRecruiter
51 - 200 Employees
Iselin, NJ, US
2018