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Assistant Biotech Quality Control Jobs in California

QC Analyst (Pharma)

Ventura, CA · On-site

$39 - $41/hr

... * Assist with execution of the stability program, including sample pulls, submissions, inventory ... biotechnology, or life sciences laboratory environment preferred. * Knowledge of laboratory ...

Orca Bio is a commercial-stage biotechnology company redefining the transplant process by ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

Designed of exotic alloys, SVF Flow Controls serves many industries including chemical, biotech ... Process, track, and follow-through on Supplier NCRs. * Assist with ISO 9001 Compliance requirements ...

QC Lab Technician

Cerritos, CA · On-site

$20 - $22/hr

Our client is a global biotechnology and aesthetics company specializing in skincare solutions. They are seeking a QC Lab Technician to join their growing team! Title: QC Lab Technician (2 Openings ...

Quality Control Technician

CA · On-site

$25 - $27/hr

Designed of exotic alloys, SVF Flow Controls serves many industries including chemical, biotech ... Process, track, and follow-through on Supplier NCRs. * Assist with ISO 9001 Compliance requirements ...

QC DIRECTOR

Rocklin, CA · On-site

$180 - $240/hr

CPC works directly with leaders in the biotechnology and pharmaceutical industries to bring ... CPC is seeking a Director of Quality Control (QC) to fill a full‑time, on‑site role in our ...

QC Lab Supervisor

Alameda, CA · On-site

$130K - $150K/yr

... Assist with root cause analysis and implementation of CAPAs. * Review laboratory notebooks ... Comfortable in a fast-paced, dynamic biotech environment with shifting priorities. * Demonstrated ...

Minimum of 8 years of progressive Quality Control experience within a regulated pharmaceutical, biotechnology, or life sciences manufacturing environment. * Minimum of 5 years of leadership ...

Showing results 41-60

Assistant Biotech Quality Control information

What is the difference between Assistant Biotech Quality Control vs Laboratory Technician?

AspectAssistant Biotech Quality ControlLaboratory Technician
CredentialsAssociate degree or equivalent, relevant certificationsAssociate degree or diploma, technical training
Work EnvironmentBiotech labs, quality assurance settingsResearch labs, clinical or industrial labs
Employer & IndustryBiotech companies, pharmaceutical firmsResearch institutions, healthcare, manufacturing
Common TasksSample testing, data recording, quality checksSample preparation, equipment operation, data collection

Assistant Biotech Quality Control and Laboratory Technicians both work in laboratory settings, often with overlapping skills. However, quality control roles focus more on ensuring product standards and compliance, while laboratory technicians may be involved in broader research or testing tasks. Understanding these differences helps job seekers target the right roles in the biotech industry.

What are the most commonly searched types of Biotech Quality Control jobs in California? The most popular types of Biotech Quality Control jobs in California are:
What job categories do people searching Assistant Biotech Quality Control jobs in California look for? The top searched job categories for Assistant Biotech Quality Control jobs in California are:
What cities in California are hiring for Assistant Biotech Quality Control jobs? Cities in California with the most Assistant Biotech Quality Control job openings:

QC Analyst (Pharma)

Astrix Inc

Ventura, CA • On-site

$39 - $41/hr

Full-time, Contractor

Re-posted 22 days ago


Job description

Pay Rate Low: 39 | Pay Rate High: 41
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!
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