Top 62 Quality specialist Jobs in Chatsworth, Ca

Quality Assurance Specialist II
Thermo Fisher Scientific —West Hills, CA
- $66,000 - $99,000 a year
- Full-time
- Background check
- Pass drug screening
- Mid-level
- Commuter assistance
- Paid parental leave
Principal Quality Systems Specialist
MiniMed —Northridge, CA
- $121,000 - $205,000 a year
- Full-time
- Microsoft Excel
- 5 years
- Office
- Health savings account
- Employee stock purchase plan
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
Quality Control Specialist
BioTalent —Santa Clarita, CA
- $28 - $32 an hour
- Urgently hiring
- Computer literacy
- Mid-level
- 3 years
Quick Apply
Quality Specialist (Final Inspection)
Crane Aerospace & Electronics —Burbank, CA
- $25.88 - $40.76 an hour
- Full-time
- Microsoft Word
- Background check
- Microsoft Excel
- Paid holidays
- Disability insurance
9d
Quality & PI Specialist
Independent Living Systems —Glendale, CA
- $85,000 - $105,000 a year
- Full-time
- Nursing
- Mid-level
- 3 years
Principal Quality Systems Specialist - CAPA
MiniMed —Northridge, CA
- $109,000 - $205,000 a year
- Full-time
- Office
- 3 years
- Project management
- Health savings account
- Employee stock purchase plan
1d
Specialist Manufacturing – Drug Product Investigation Support
Amgen —Thousand Oaks, CA
- $107,545.40 - $145,502.60 a year
- Doctoral degree
- Mid-level
- Master's degree
- Disability insurance
- Health insurance
Experienced Aerospace Quality Specialist
Align Aerospace —Chatsworth, CA
- $34 - $37 an hour
- Full-time
- Mid-level
- 3 years
- Ability to lift 50 pounds
- Paid training
- Paid holidays
Quick Apply
14d
Quality Systems Specialist - III
Katalyst Healthcares & Life Sciences —Santa Monica, CA
- Contract
- 5 years
- Analysis skills
- Senior level
Quick Apply
Supply Chain Specialist - Quality
PBS Biotech Inc —Camarillo, CA
- $38.61 - $49.18 an hour
- Full-time
- Mid-level
- Office
- Organizational skills
Quick Apply
Quality Outreach Specialist
Los Angeles LGBT Center —Los Angeles, CA
- $31.06 - $33.24 an hour
- Full-time
- Spanish
- Medical office experience
- Mid-level
- Disability insurance
- Health insurance
Quick Apply
13d
Sales Quality & Customer Support Specialist
Cydcor —Agoura Hills, CA
- $55,000 - $60,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Electronics Quality Specialist - 2nd Shift 2:00 p.m. to 10:30 p.m
Curtiss-Wright —Santa Clarita, CA
- $25.38 - $33.85 an hour
- Full-time
- Schematics
- 5 years
- Mid-level
- Profit sharing
- Employee stock purchase plan
Quick Apply
Federal QCM and QC Professionals – CQM Required Preferred
Elite Recruiting & Consulting Services —Los Angeles, CA
- Online Application
- Construction site
- Mid-level
- Travel
Quick Apply
Federal Construction Professionals – QCM, Superintendent, PM
Elite Recruiting & Consulting Services —Los Angeles, CA
- Online Application
- OSHA
- Construction site
- Travel
Quick Apply
QA Admin Specialist
Hydraulics International —Chatsworth, CA
- $20 - $25 an hour
- Overtime
- Customer service
- Computer literacy
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Quality Control Specialist, Microbiology
Amgen —Thousand Oaks, CA
- $100,450.45 - $135,903.55 a year
- Doctoral degree
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance
Test Specialist, Self-Driving (Afternoon Shift)
Tesla —Marina del Rey, CA
- $22.80 - $39.90 an hour
- Full-time
- Mid-level
- Driving
- Travel
- Commuter assistance
- Health savings account
Sales Quality Specialist
Cydcor —Agoura Hills, CA
- $55,000 - $60,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Health insurance
- Dental insurance
Quick Apply

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Quality Assurance Specialist II

Thermo Fisher Scientific -
West Hills, CA

Apply Now

Job Details

Full-time
$66,000 - $99,000 a year

Benefits

Commuter assistance
Paid parental leave
Caregiver leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
Life insurance

Qualifications

Optimizing workflow processes
Statistics
Computer operation
Defect resolution root cause analysis
Safety protocol adherence
Technical documentation
ISO standards
Spreadsheets
Project management experience in manufacturing
Production validation processes
Bachelor's degree
Quality risk management
Automated systems
Quality control problem-solving
Presentation preparation
Biomedical regulatory compliance
Productivity software
Continuous process improvement (CPI)
Manufacturing company experience
Technical Proficiency
Failure analysis
Analytics

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

The Quality Assurance team is responsible for reviewing equipment validations, process validations, change control, technical transfers, and new product initiatives for RUO and IVD TDX HLA Typing kits and reagents. Validation work includes the ability to perform risk assessments to identify the extent of validation required. The QA Specialist II position requires the ability to write/review protocols and write/review reports for validation and new design processes. The application of risk assessment methodology is required for this
position in order to support a fast-paced Change Control system while maintaining all IVD Compliance Requirements, where applicable. Technical Transfer activities include reviewing protocols and reports along with cross functional collaboration during the design control process in order to develop robust
manufacturing processes, QC methods, and documentation to support the DMR. The QA Specialist II may sit on Core Teams or assist the Core Team in developing processes and transferring knowledge between
different teams. This position is constantly cross functional in nature and requires independent thought and schedule adherence, under moderate levels of guidance.

Location: West Hills, CA. Relocation assistance is NOT provided.

Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.

Key Responsibilities:

Review validation projects, protocols, and reports in support of equipment and process validation.
Write and review protocols and reports.
Review IQ/OQ protocols and reports.
Assist in Risk Assessment exercises in support of validation activities.
Collaborate with R&D, Product Development Manager, Technical Operations, and Operations to
ensure successful process development and technical transfers.
Coordinate validation activities/reviews in support of assigned validation projects working closely
Subject Matter Experts.
Recommend approval or failure of validation studies.
Maintain knowledge and comprehensive understanding of relevant Medical Device regulations and current interpretations affecting equipment, product and process validation.
Act as a resource to other departments for product and process knowledge.
Able to work independently, with guidance from the Quality Assurance team.
Ability to learn new products and technology.
Able to successfully lead a project involving a peer group.
Lead and/or participate in product related team meetings and/or performance reviews, as needed.
Assist with QA department functions as needed. (Specific duties may vary and will be documented in department records, job assignments and/or project action items).
Perform computer operations for data entry and provide tracing/trending reports.
Additional support of routine QA department standard operating procedures (SOPs) is also
expected when necessary.
Exhibits a high level of quality (right the first time), integrity (do what you say you are going to do), and cross functional behavior (always stay above the line).

Minimum Requirements:

Bachelor’s degree in Biology, Chemistry, or other similar Life Science field.
3+ years relevant experience in Quality regulated environment
Detailed knowledge of ISO and GMP regulations which govern a medical device and diagnostics manufacturing
Able to create presentations, work with spreadsheets, prepare reports and write procedures utilizing MS Word, Excel and PowerPoint software applications.
Consistently demonstrated validation proficiency, with knowledge of equipment qualification (IQ/OQ/PQ), process validation, and computer/automation systems.
Good analytical skills, with an ability to use scientific knowledge and statistical methods to identify root causes of process and product failures.
Strong project management and organizational skills.
Demonstrated technical skills in process validation & concepts with an emphasis on implementation.
Excellent verbal and written communication skills.
Previous experience in problem solving methodology.
Possess a continuous process improvement mindset with the ability to effectively lead and manage change.
Performs all job duties in a safe manner, consistent with the Code of Ethics and the Thermo Fisher Scientific 4-I core values of Integrity, Intensity, Innovation, and Involvement.
Performs other duties as assigned

Compensation and Benefits

The salary range estimated for this position based in California is $66,000.00–$99,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Apply Now

Refine Your Search

quality specialist jobs in chatsworth, ca

Quality Assurance Specialist II

Principal Quality Systems Specialist

Quality Specialist II, Product Release and Label Management

Quality Control Specialist

Quality Specialist (Final Inspection)

Quality & PI Specialist

Principal Quality Systems Specialist - CAPA

Specialist Manufacturing – Drug Product Investigation Support

Experienced Aerospace Quality Specialist

Quality Systems Specialist - III

Supply Chain Specialist - Quality

Quality Outreach Specialist

Sales Quality & Customer Support Specialist

Electronics Quality Specialist - 2nd Shift 2:00 p.m. to 10:30 p.m

Federal QCM and QC Professionals – CQM Required Preferred

Federal Construction Professionals – QCM, Superintendent, PM

QA Admin Specialist

Quality Control Specialist, Microbiology

Test Specialist, Self-Driving (Afternoon Shift)

Sales Quality Specialist

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