Top 7 Biotechnology quality assurance Jobs in Los Angeles Ca

Supervisor, Quality Control
Kite Pharma —El Segundo, CA
- $107,185 - $138,710 a year
- Full-time
- 5 years
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
12d
Quality Specialist II, Product Release and Label Management
Thermo Fisher Scientific —West Hills, CA
- $66,000 - $99,000 a year
- Full-time
- Mid-level
- 3 years
- Analysis skills
- Commuter assistance
- Paid parental leave
QA/QC Director
ProcessHQ, Inc. —Glendale, CA
- $100,000 - $200,000 a year
- Full-time
- Management
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Senior Manager, Clinical and PV Quality Assurance (Inspection Readiness and Management)
Arrowhead Pharmaceuticals —Los Angeles, CA
- $145,000 - $170,000 a year
- Office
- 8 years
- Bachelor's degree
1d
Validation Specialist
Katalyst Healthcares & Life Sciences —Los Angeles, CA
- Contract
- 5 years
- Engineering
- English
Quick Apply
Temporary - Senior Associate, QC Stability and Reference
ImmunityBio —Culver City, CA
- $35.50 - $39.00 an hour
- Full-time
- Microsoft Excel
- Mid-level
- Bachelor's degree
- AD&D insurance
- Disability insurance
11d
Manager, Clinical Quality System Documents
Arrowhead Pharmaceuticals —Los Angeles, CA
- $120,000 - $145,000 a year
- Microsoft Word
- 5 years
- Bachelor of Science
1d

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Quality Assurance Specialist
GIT America Inc. —Irvine, CA
Bachelor’s degree in automotive/mechanical engineering degree is a plus. US citizenship preferred for port entry. 401K plan with company matching.
$50,000 - $60,000 a year
Quick Apply
Quality Inspector - Aerospace
Sourcing HR Solutions —Valencia, CA
Your keen eye for detail, technical expertise, and commitment to excellence will contribute significantly to maintaining the highest levels of safety,…
$26 - $36 an hour
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PSC Biotech —Columbus, OH
Minimum of 3 years of experience in computerized system validation, automation software, and manufacturing systems within regulated life science industries (i.e…

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Supervisor, Quality Control

Kite Pharma -
El Segundo, CA

Apply Now

Job Details

Full-time
$107,185 - $138,710 a year
12 days ago

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
Life insurance

Qualifications

Practicing in a sourcing or procurement role
Biotechnology
Raw material quality management
Immunological assays
Operations management
Laboratory procurement
Laboratory equipment maintenance
Team leadership
Managing laboratory operations teams
Immunological laboratory techniques
5 years
Bachelor of Science
Production deviation management
Routine inspections
Corrective and preventive actions (CAPA)
FDA 21 CFR Part 11
GMP
Mid-level
Flow cytometers
Quality reports
High school diploma or GED
Team development
ICH guidelines
Laboratory reports
Supervising experience
Laboratory quality control records management
Bachelor's degree
Pharmaceutical company experience
Scientific protocols
Team training

Full Job Description

Job Description

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Job Description

**Shift: Wednesday-Saturday, 12:00pm-10:30pm**

Specific Responsibilities (including but are not limited to):

Lead a team of high-performing individuals, with particular focus on individual development in support of greater team achievement.
Drive a culture of Operational Excellence in the group.
Supervise Analytical QC testing and various other support activities performed in the Analytical QC Lab.
Review of records, generation of CoAs for product release. Complete routine record review of test data and related documents for in-process testing, drug substance and drug product release.
Responsible for overseeing on-time completion of training for the group.
Monitor GMP systems currently in place to ensure compliance with documented policies.
Expectation includes a hands-on, collaborative approach to problem solving, planning, and people-management.
Participate in and support development and implementation of Operational Excellence initiatives to enhance laboratory and staff efficiencies.
Participate and/or lead daily and weekly team meetings.
Work with internal and external resources to maintain analytical equipment in an optimal state.
Oversee purchase and qualification of equipment, materials and media required for routine testing and reagent qualification.
Responsible for OOS, lab and protocol deviations, and corrective action plan implementation when necessary.
Provides input and support in the development, revision and review of SOPs, protocols and reports.
Participate in inspections by both internal and external stakeholders as needed.

Basic Qualifications:

MA / MS Degree with 3+ years of analytical and/or cGMP operations and/or quality experience OR
BA/BS Degree with 5+ years of analytical and/or cGMP operations and/or quality experience OR
High School Degree with 9+ years of analytical and/or cGMP operations and/or quality experience

Preferred Qualifications:

Experience supervising/managing analytical labs within the biotechnology or pharmaceutical industry.
Demonstrated guidance and overseeing skills, including establishing direction and goals, and guiding implementation while fostering a team-based environment.
Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environment.

Experience in any of the following analytical techniques, Flow Cytometry, PCR, ELISA, cell viability measurement.
Familiarity with FDA, EU and ICH guidelines.
Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211), Quality Control, GMPs, GLP.
Comfortable in a fast-pace company environment with minimal direction and able to adjust workload based on changing priorities.
Ability to think critically and demonstrate troubleshooting/problem solving skills.
Excellent skills in Microsoft Office, data analysis software, and other related applications.

The salary range for this position is: $107,185.00 - $138,710.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Kite Pharma Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Apply Now

Refine Your Search

biotechnology quality assurance jobs in los angeles ca

Supervisor, Quality Control

Quality Specialist II, Product Release and Label Management

QA/QC Director

Senior Manager, Clinical and PV Quality Assurance (Inspection Readiness and Management)

Validation Specialist

Temporary - Senior Associate, QC Stability and Reference

Manager, Clinical Quality System Documents

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