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Pharmaceutical Qa Jobs in Riverside, CA (NOW HIRING)

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Seeking a QA Inspector familiar with the biosciences field who can check incoming and outgoing ... pharmaceutical, or biotech environment. · Computer skills including Microsoft Word, Excel, and ...

... pharmaceutical and biotechnology clients. Why Forma? Unlike large, highly layered organizations ... Requirements Job Overview/Summary The Specialist supports Quality Assurance activities regarding ...

... pharmaceutical and biotechnology clients. Why Forma? Unlike large, highly layered organizations ... Requirements Job Overview/Summary The Specialist supports Quality Assurance activities regarding ...

The (USA) Specialist, Quality Assurance is responsible for executing operational analyses to ... pharmaceuticals. By promoting compliance and ethical standards, this position contributes to ...

The (USA) Specialist, Quality Assurance is responsible for executing operational analyses to ... pharmaceuticals. By promoting compliance and ethical standards, this position contributes to ...

Onsite Stryker is hiring an Associate Manager, Quality Assurance in Irvine, CA to lead a high ... Minimum of 6+ years' experience in a Medical, Pharmaceutical, Bio-Medical/Pharma, Automotive or ...

QA Auditor

Tustin, CA · Hybrid

$103K - $129K/yr

Serves as the QA subject matter expert in the creation and revision of Raw Material Specifications ... S. degree (preferably in Life Science) and 5+ years of experience in the pharmaceutical ...

QA Auditor

Tustin, CA · On-site

$103K - $129K/yr

Serves as the QA subject matter expert in the creation and revision of Raw Material Specifications ... S. degree (preferably in Life Science) and 5+ years of experience in the pharmaceutical ...

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Pharmaceutical Qa information

See Riverside, CA salary details

$11

$48

$76

How much do pharmaceutical qa jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for pharmaceutical qa in Riverside, CA is $48.73, according to ZipRecruiter salary data. Most workers in this role earn between $31.11 and $64.71 per hour, depending on experience, location, and employer.

What is a pharmaceutical QA?

Pharmaceutical QA (Quality Assurance) professionals are responsible for ensuring that pharmaceutical products are developed, manufactured, and distributed according to industry standards and regulatory requirements. Their main goal is to maintain product quality and safety by overseeing processes, conducting audits, and implementing quality management systems. They work closely with other departments to ensure compliance with Good Manufacturing Practices (GMP) and other regulations. QA professionals also investigate quality issues, review documentation, and facilitate continuous improvement to prevent future problems.

Is pharmaceutical QA a good career?

Pharmaceutical QA (Quality Assurance) is a stable career that involves ensuring drug manufacturing processes meet regulatory standards and quality requirements. It typically requires attention to detail, knowledge of Good Manufacturing Practices (GMP), and relevant certifications. The role offers opportunities for advancement and employment in the healthcare and biotech industries.

What is the difference between Pharmaceutical Qa vs Pharmaceutical Quality Control Analyst?

AspectPharmaceutical QaPharmaceutical Quality Control Analyst
CertificationsGMP, GDP, ISO certificationsGMP, GLP, ISO certifications
Work EnvironmentQuality assurance departments, regulatory complianceLaboratories, testing facilities
Primary FocusEnsuring quality processes and complianceTesting and analyzing raw materials and products

Pharmaceutical Qa professionals focus on maintaining quality standards through audits, documentation, and compliance, while Pharmaceutical Quality Control Analysts perform laboratory testing to verify product quality. Both roles are essential in the pharmaceutical industry and often work closely to ensure products meet regulatory requirements.

What are some common challenges faced by pharmaceutical QA professionals, and how can they be addressed?

Pharmaceutical QA professionals often encounter challenges such as staying up-to-date with evolving regulatory requirements, managing complex documentation, and ensuring consistent product quality across batches. To address these issues, QA teams typically participate in regular training, implement robust quality management systems, and foster close collaboration with production, R&D, and regulatory affairs departments. Effective communication and proactive problem-solving are also key to maintaining compliance and quickly resolving quality issues as they arise.

What are the key skills and qualifications needed to thrive as a pharmaceutical QA, and why are they important?

To thrive as a Pharmaceutical QA, you need a strong background in quality assurance processes, regulatory compliance, and a relevant scientific degree such as pharmacy, chemistry, or biology. Familiarity with Good Manufacturing Practices (GMP), quality management systems (QMS), and industry-standard audit tools or certifications like ISO 9001 is essential. Attention to detail, analytical thinking, and strong communication skills help professionals excel in identifying issues and ensuring adherence to standards. These skills are crucial for maintaining product safety, meeting regulatory requirements, and upholding a company’s reputation in the pharmaceutical industry.

How to become a pharmaceutical QA?

To become a pharmaceutical QA, candidates typically need a bachelor's degree in pharmacy, chemistry, or a related field, along with knowledge of Good Manufacturing Practices (GMP) and quality assurance processes. Gaining experience through internships or entry-level roles in pharmaceutical manufacturing or quality control is also important, and professional certifications like ASQ Certified Quality Auditor can enhance prospects.
What are popular job titles related to Pharmaceutical Qa jobs in Riverside, CA? For Pharmaceutical Qa jobs in Riverside, CA, the most frequently searched job titles are:
What cities near Riverside, CA are hiring for Pharmaceutical Qa jobs? Cities near Riverside, CA with the most Pharmaceutical Qa job openings:
Infographic showing various Pharmaceutical Qa job openings in Riverside, CA as of August 2026, with employment types broken down into 85% Full Time, 4% Part Time, and 11% Contract. Highlights an 96% In-person, and 4% Hybrid job distribution, with an average salary of $101,348 per year, or $48.7 per hour.

QA Compliance Lead - Afternoons

Bimeda Inc.

Pomona, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago


Job description

Job Title: QA Compliance Lead - Afternoons (2:00p.m. to 10:30p.m.)
Location:Pomona, CA (In-office)
Position Type: Full-time,
Vacancy Status:This position is vacant
AI Disclosure in Hiring:We use artificial intelligence to screen, assess and select applicants


Purpose of the Position/ Role Summary

The QA Compliance Lead is the senior-most QA Compliance resource supporting manufacturing operations and serves as the primary day-to-day quality lead.

This role ensures consistent execution of cGMP compliance activities, including batch record review, deviation investigations, CAPA oversight, and audit readiness. The Lead acts as a key partner to the QA Manager by driving quality processes, supporting regulatory readiness, and providing guidance to QA Compliance Associates.


Key Responsibilities
Own day-to-day QA compliance activities across manufacturing, ensuring timely batch review and product release in accordance with GMP standards.
QA oversight of manufacturing, including label control and issuance and in-process inspections.
Lead deviation investigations, OOS events, and non-conformances, including root cause analysis and CAPA development.
Review and approve QA documentation (batch records, deviations, CAPAs) prior to QA Manager escalation where required.
Serve as primary QA contact on the floor, providing real-time guidance to Associates, operators, and supervisors.
Conduct and support internal audits to ensure adherence to SOPs, cGMP, and regulatory requirements.
Support regulatory inspections and customer audits, including preparation, hosting support, and follow-up actions.
Monitor QA systems and quality trends, escalating risks and recommending improvements.
Support SOP and document updates to maintain compliance and operational efficiency.
Coach and mentor QA Compliance Associates on investigations, documentation, and GMP expectations.
Partner cross-functionally with Operations, QC, and other teams to drive a culture of quality and compliance.


Additional Notes:
Working conditions: warehouse and production environments. Exposure to noise, chemicals and machinery. PPE required in certain areas.
Physical demands: Walking, standing, occasional lifting (up to 50 pounds).
May require work outside regular hours or weekends.


Please note that this job description is not exhaustive, and the role holder may be required to undertake other relevant duties commensurate with the grading of the post. Activities may be subject to amendment over time as the role develops and/or priorities and requirements evolve.


Competencies Required for the Role

EFFECTIVE COMMUNICATION - Is the ability to convey information to another effectively and efficiently, to listen - help facilitate sharing of information between people. It is about understanding the emotional intention behind the information. The ability to express oneself clearly in conversations, confirm understanding, communicate using data and facts. Exhibit willingness to listen and show respect for oneself and others in interactions with others. Express oneself clearly in verbal and business writing.
FOSTERING COLLABORATION/TEAMWORK - is the ability to work jointly with others or together especially in an intellectual endeavor; the ability and desire to work cooperatively with others on a team; as a team leader, the ability to demonstrate interest, skill, and success in getting groups to learn to work together. Builds partnerships for global performance. Respects others.
ANALYTICAL THINKING/PROBLEM SOLVING - is the ability to identify the information needed to clarify a situation, seek that information from various sources and then tackle a problem by using a logical, systematic, sequential approach. Ability to identify and separate the key components of problems and situations. Ability to interpret information from a range of sources to spot patterns and trends in information and to deduce cause and effect from this.
RESULTS ORIENTATION - The ability to focus on the desired result of one's own department's work, setting challenging goals, focusing on the goals, and meeting or exceeding them.


Qualifications & Experience

  • 5-7 years in pharmaceutical QA / GMP environment
  • Strong experience in:

- Batch record review & product release

- Deviation investigations & CAPA systems

- Audit support (FDA/customer)

  • Demonstrated ability to work independently and make quality-based decisions
  • Strong technical writing and documentation skills
  • Proven ability to coach others without formal authority


What We Offer
Health Insurance (medical, dental, vision)
401(k) plan for retirement savings
Paid time off (vacation, sick leave, holidays)
Life insurance
Employee assistance program


About Bimeda
Bimeda is a leading global innovator, manufacturer and marketer of veterinary pharmaceuticals and animal health products and has over half a century's experience in providing science-driven solutions to optimize the health, wellbeing and productivity of the world's animals.


Bimeda's global innovation program sees eight state-of-the art R&D centers across four continents collaborate on an enviable product development pipeline which anticipates the ever-evolving needs of the animal health industry.


Bimeda's nine manufacturing facilities across seven countries allow the company to manufacture a broad range of preventative, curative and nutritional products including sterile injectables, vaccinations, nutritional boluses, feed additives, tablets, water-soluble powders, pastes and non-sterile liquids.


Globally, the company focuses on the development, manufacture and commercialization of quality Bimeda-branded products while also being the partner of choice for contract manufacturing and R&D services for prominent companies within the animal health industry.


More info at www.bimedacareers.com


Bimeda is an equal opportunity employer committed to fostering a diverse workforce. All qualified applicants will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.