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Vaco by Highspring

Quality Control Analyst

Shavano Park, TX · Hybrid

$21.50 - $29/hr

Quality Control Analyst (QCA) Location: San Antonio, TX Schedule: Onsite 5 days/week | 8:30 AM - 5:30 PM Duration: 6 Month Contract (Potential Extension) No sponsorship or visas available. Overview ...

Actalent

Surgical Technician

Minneapolis, MN

Familiarity with QCA or QVA measurements and associated documentation practices. * Experience operating fluoroscopy, 3D imaging, or other software-driven imaging and surgical systems is a plus.

Actalent

Surgical Technician

Minneapolis, MN · On-site

Familiarity with QCA or QVA measurements and associated documentation practices. * Experience operating fluoroscopy, 3D imaging, or other software-driven imaging and surgical systems is a plus.

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How much do qca jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for qca in the United States is $21.73, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.00 per hour, depending on experience, location, and employer.

What jobs pay 500,000 a year in the US?

For a QCA (Quality Control Analyst) or similar roles, earning $500,000 annually is uncommon and typically requires executive-level positions, extensive experience, or ownership in a business. High-paying jobs in this range are more often found in executive management, investment banking, or specialized medical fields, often involving advanced certifications and long-term career development.

What profession makes $400,000 a year?

In the field of quality control analysis (QCA), senior professionals such as quality assurance directors or managers in large corporations can earn around $400,000 annually, especially with extensive experience, advanced certifications, and leadership responsibilities. High-level roles in industries like pharmaceuticals, manufacturing, or technology tend to offer such compensation levels.

What jobs pay $10,000 a month without a degree?

Jobs such as sales managers, real estate brokers, and certain skilled trades like electricians or plumbers can earn $10,000 or more per month without a college degree, often through commissions, bonuses, or high hourly rates. Success in these roles typically depends on experience, skills, and performance rather than formal education.

What are the key skills and qualifications needed to thrive as a Quality Control Analyst (QCA), and why are they important?

To thrive as a Quality Control Analyst, you need a strong background in laboratory science, analytical techniques, and attention to detail, usually supported by a degree in chemistry, biology, or a related field. Familiarity with laboratory instruments (like HPLC, GC, or spectrophotometry), GMP regulations, and relevant certifications (such as ISO or FDA compliance) is often required. Excellent problem-solving skills, communication, and organization help QCAs work efficiently and ensure accurate reporting. These competencies are essential for maintaining product quality, regulatory compliance, and the integrity of testing processes.

What are some common challenges faced by QC Analysts (QCA) when working in a fast-paced laboratory environment?

QC Analysts often encounter tight deadlines due to production schedules and regulatory requirements, which can add pressure to deliver accurate results quickly. Adapting to frequently updated testing protocols and ensuring compliance with quality standards are also key challenges. Effective communication and collaboration with production and R&D teams are essential for troubleshooting issues and maintaining workflow. Staying organized and detail-oriented helps QC Analysts manage multiple tests and documentation efficiently, contributing to the overall success of the quality assurance process.

Is QA a difficult job?

Quality Assurance (QA) jobs can be challenging as they require attention to detail, understanding of testing processes, and knowledge of tools like test management software. The difficulty level depends on the complexity of the projects and the experience of the QA professional, but it generally involves problem-solving and continuous learning.

What are QCAs?

QCAs, or Quality Control Analysts, are professionals responsible for testing and verifying the quality of products in industries like pharmaceuticals, food, and manufacturing. They conduct laboratory tests, analyze data, and ensure that products meet regulatory and company standards. QCAs play a critical role in identifying defects, maintaining compliance, and supporting continuous improvement processes. Their work helps ensure consumer safety and product reliability.
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Qca jobs near you
Director, Commercial QCA

Director, Commercial QCA

ImmunityBio, Inc.

Culver City, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

Job description

Company Overview
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease.
Why ImmunityBio?
• ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
• Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
• Work with a collaborative team with the ability to work across different areas of the company.
• Ability to join a growing company with professional development opportunities.
Position Summary
The Director, Commercial QCA is responsible for the design, planning, implementation, and operation control of quality control programs to ensure product reliability, quality, efficacy, and compliance to applicable state, federal, and country-specific regulations including cGMPs and internal standards for manufacturing, materials and finished products related to the commercial N-803 program and all other QCA programs that are advancing to the commercial stage..
Essential Functions
  • Ensure the compliant (in line with all relevant guidance), efficient operations of Quality Control Analytical by overseeing all laboratory testing (in house and outsourced In Process, Lot Release, and Stability).
  • Transfer, review, and approve methods and documentation including product specifications; protocols, SOPs, reporting of testing, analytical method development and validation and stability studies.
  • Ownership and oversight of all assay trending programs
  • Design and implement methods to increase efficiencies and productivity, and to improve knowledge of product safety, purity, efficacy, potency, and stability. Design and implement strategies to transfer methods into QCA groups.
  • Ensure QCA decisions align with Quality System, GMP and regulatory requirements.
  • Provide budgets for current and future operations including strategy and plans for laboratory relocations and new laboratory implementation.
  • Develop and mentor the Analytical Quality Control staff to perform at a commercial level of compliance.
  • Oversee the performance of designated staff. Responsibilities include interviewing, hiring and training employees, planning, assigning and directing work; appraising performance; rewarding and disciplining employees, addressing complaints and resolving problems.
  • Performs ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities.

Education & Experience
  • Bachelor's degree in biology, chemistry, or other scientific related field with 15 years of related quality experience with 8+ years at the management level required; or
  • Master's degree in biology, chemistry, or other scientific related field with 10 years of related quality experience with 8+ years at the management level required; or
  • Ph.D. in biology, chemistry, or other scientific related field with 8+ years of related quality experience with 8+ years at the management level required
  • Extensive experience with assay qualification, validation, and transfer activities required
  • Experience for a FDA PLI, Surveillance, or other inspection, with an acceptable outcome required
  • Experience with a start-up pharmaceutical company preferred

Knowledge, Skills, & Abilities
  • Thorough understanding of biologics manufacturing processes, including cell culture, purification, and analytical characterization techniques. Understanding of cell therapy processes is desirable
  • Proven track record of successfully leading QC teams, driving quality initiatives, and managing regulatory inspections
  • Strong organizational skills, attention to detail, and ability to prioritize and manage multiple projects simultaneously
  • Excellent communication skills, with the ability to effectively interact with cross-functional teams, senior management, and external entities
  • In-depth knowledge in analytical method development and validation, and statistical quality control.
  • In-depth knowledge of GMPs, SOPs and pharmaceutical regulations.
  • Ability to use sound scientific judgment in management of the facility and processes to prevent regulatory action.
  • Understanding of GMPs and an ability to interpret and enforce regulatory requirements.
  • Ability to communicate professionally, knowledgeably, and efficiently with a wide range of employees and with all internal and external customers, both in writing and verbally.
  • Ability to work with contractors and suppliers, ensuring compliance with company standards and contractor systems.
  • Ability to define problems, collect data, establish facts and draw valid conclusions.
  • Demonstrated track record in managing a staff and establishing a clear, strategic direction.
  • Ability to develop a high-morale organization with leaders, teams, and groups, and appropriately staff the QC department to meet business needs.
  • Ability to analyze and interpret complex, scientific documents, including problem solving.
  • Ability to multi-task and prioritize with excellent project management skills.

Working Environment / Physical Environment
  • This role will work on site
  • Flexibility in working schedule, i.e., off-hours, second shift and weekends as needed
  • Performs work in the lab as needed to supervisor staff and oversee quality control programs
  • Must be able to gown PPE as needed to enter lab settings

This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.
$215,000 (entry-level qualifications) to $236,500 (highly experienced) annually
The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.
ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO) includes: 11 Holidays • Exempt Employees are eligible for Unlimited PTO • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day • We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.
At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

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