Top 259 Qc analyst Jobs

QC Analyst (Pharma)
Astrix Technology Group —Ventura, CA
- $39 - $41 an hour
- Full-time
- Mid-level
- Bachelor's degree
- Organizational skills
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QC Analyst
System One —Orangeburg, NY
- $21 - $23 an hour
- Contract
- Bachelor's degree
- Critical & Intensive Care
- Cleaning
- Health insurance
- Dental insurance
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13d
QC Lab Analyst
Astrix Technology Group —Cincinnati, OH
- $25 an hour
- Contract
- Mid-level
- Databases
- Math
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Quality Control Analyst
System One —Vienna, VA
- $40 - $60 an hour
- Contract
- Hybrid work
- Background check
- Research
- Mid-level
- Health insurance
- Dental insurance
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6d
QC Analyst- 2nd Shift
Nesco Resource, LLC —Troy, NY
- $23 - $25 an hour
- Contract
- Bachelor of Science
- High school diploma or GED
- Bachelor's degree
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QC Analyst
Validation & Engineering Group —Manatí, PR
- Full-time
- Bachelor's degree
- 1 year
- Entry level
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Quality Engineer/Data Analyst
ESTIS MANAGEMENT LLC —Midland, TX
- 5 years
- Bachelor of Science
- Engineering
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QC Analyst II, 2nd Shift
Piramal Pharma Solutions —Sellersville, PA
- Full-time
- Bachelor's degree
- US work authorization
- In-person
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Quality Control Analyst
Lenox Executive Search —Lexington, MA
- $38 an hour
- Full-time
- Maintenance
- Microsoft Office
- Bachelor's degree
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5d
Quality Lab Analyst
Givaudan —East Hanover, NJ
- $24 - $25 an hour
- 12 hour shift
- Computer literacy
- Data analysis skills
- English
- Health insurance
- Dental insurance
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Quality Control Analyst - II
Rensselaer, NY Client —Rensselaer, NY
- $63,000 - $79,000 a year
- 12 hour shift
- Background check
- Mid-level
- 3 years
- Paid training
- Paid holidays
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Associate Quality Control Analyst (Part Time)
DraftKings —Raleigh, NC
- $17 an hour
- Part-time
- Analysis skills
- APIs
- Communication skills
Quality Control Analyst
Zillion Technologies —Winchester, VA
- $24 an hour
- Full-time
- Hybrid work
- Word processing
- Research
- Mid-level
- Disability insurance
- Health insurance
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7d
FAA Quality Analyst
TAD PGS, Inc —Torrance, CA
- $27 an hour
- Contract
- Writing skills
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
7d
Quality Control Analyst
Corvant —Lithia Springs, GA
- Full-time
- Construction site
- Ability to walk for extended periods
- Engineering
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Quality Control Analyst
Corvant —Covington, GA
- Full-time
- Construction site
- Ability to walk for extended periods
- Engineering
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Quality Control Analyst
Corvant —Madison, MS
- Full-time
- Construction site
- Ability to walk for extended periods
- Engineering
Quick Apply
Sentinel - Principal Configuration Analyst - Audit - 18011*
Northrop Grumman —Huntsville, AL
- $89,900 - $134,900 a year
- Overtime
- Up to 50% travel
- 5 years
- Master's degree
- Paid holidays
- Disability insurance
7d
QA Analyst I (2nd Shift)
The Marzetti Company —Columbus, OH
- Overtime
- Bachelor's degree
- Computer skills
- Ability to stand for extended periods
Quality Control Analyst
VITALITY WORKS INC —Albuquerque, NM
- $24 - $28 an hour
- Full-time
- Microsoft Outlook
- Bachelor of Science
- Mid-level
- Health savings account
- AD&D insurance
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QC Analyst (Pharma)

Astrix Technology Group -
Ventura, CA

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Job Details

Full-time | Contract
$39 - $41 an hour

Qualifications

Laboratory sample storage
Data integrity assurance
Biology
Biotechnology
Stability testing
Biochemistry
Laboratory inventory control
Biological sample management
Investigations regulatory compliance
Quality records maintenance
Laboratory equipment routine checks
Stability studies in drug product development
Shipping coordination
Pharmaceutical laboratory environment
Pharmaceutical regulatory compliance
Labeling
Good documentation practices (GDP)
Mid-level
Laboratory test results documentation
Laboratory equipment calibration
Bachelor's degree in biology
Manufacturing standard operating procedures
Laboratory quality control records management
Bachelor's degree
Quality assurance standard operating procedures
Pharmaceutical company experience
Pharmaceutical analysis
Laboratory standard operating procedures
Compliance documentation
Bachelor's degree in pharmaceutical sciences

Full Job Description

Our client, a global CDMO, offering products and services across the drug development spectrum is looking for a skilled QC Analyst to join their team in Camarillo, CA!

Location: Ventura County, CA
Pay rate: $39- $41/hr.
Job type: 6-month contract (possibility of extension or conversion)

Position Summary
The QC Analyst is responsible for supporting routine laboratory testing, sample management, stability program activities, and quality system requirements within a cGMP-regulated environment. This role ensures accurate testing, documentation, and data integrity while collaborating cross-functionally to support product quality and operational timelines.

Key Responsibilities

Perform routine QC laboratory testing using analytical techniques including pH, Osmolality, and FT-IR for in-process, finished product, and stability samples.
Support sample management activities including sample receipt, login, labeling, tracking, storage, inventory control, and shipment coordination.
Assist with execution of the stability program, including sample pulls, submissions, inventory management, tracking, and documentation activities.
Maintain accurate and complete documentation in compliance with cGMP, ALCOA+, data integrity requirements, and company procedures.
Record and review laboratory data in notebooks, worksheets, logbooks, and electronic systems, ensuring records remain audit-ready at all times.
Participate in laboratory investigations related to out-of-specification (OOS) results, deviations, invalid assays, and other quality events.
Support laboratory maintenance activities including equipment calibration, routine housekeeping, inventory management, and inspection readiness.
Collaborate with Quality Assurance (QA), Manufacturing, Stability, Microbiology, and external testing laboratories to ensure timely completion of testing and operational objectives.
Follow approved Standard Operating Procedures (SOPs), test methods, and GMP laboratory procedures with minimal supervision.

Qualifications

Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline preferred.
1-3 years of experience working in a cGMP-regulated pharmaceutical, biotechnology, or life sciences laboratory environment preferred.
Knowledge of laboratory analytical techniques, quality systems, data integrity principles, and regulatory requirements.
Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
Excellent attention to detail, documentation practices, and problem-solving abilities.
Effective communication and teamwork skills with the ability to work cross-functionally.
Proficiency with laboratory documentation systems and Microsoft Office applications.

Note: This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

INDBH
#LI-AH1

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