Qualifications & Experience * 5-7 years in pharmaceutical QA / GMP environment * Strong experience in: - Batch record review & product release - Deviation investigations & CAPA systems - Audit ...
Qualifications & Experience * 5-7 years in pharmaceutical QA / GMP environment * Strong experience in: - Batch record review & product release - Deviation investigations & CAPA systems - Audit ...
The specialist oversees QA and technical documents according to FDA and other applicable regulatory ... pharmaceutical quality systems experience strongly preferred;
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The specialist oversees QA and technical documents according to FDA and other applicable regulatory ... pharmaceutical quality systems experience strongly preferred;
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Quality Assurance Inspector
Santa Ana, CA · On-site
$20 - $24/hr
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 ...
Quick apply
Be Seen First
Quality Assurance Inspector
Santa Ana, CA · On-site
$20 - $24/hr
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 ...
Vice President, Quality Assurance
Irvine, CA · On-site +1
$280K - $327K/yr
Quality Assurance REPORTING TO: Chief Operating Officer LOCATION: An Ambros corporate office or ... Bachelor's degree or higher in life sciences, chemistry, pharmaceutical sciences, or related field ...
Vice President, Quality Assurance
Irvine, CA · On-site +1
$280K - $327K/yr
Quality Assurance REPORTING TO: Chief Operating Officer LOCATION: An Ambros corporate office or ... Bachelor's degree or higher in life sciences, chemistry, pharmaceutical sciences, or related field ...
As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards ... Your Role: The QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which ...
As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards ... Your Role: The QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which ...
Quality Assurance Specialist
Irvine, CA · On-site
$71K - $85K/yr
... pharmaceutical and biotechnology clients. Why Forma? Unlike large, highly layered organizations ... Requirements Job Overview/Summary The Specialist supports Quality Assurance activities regarding ...
Quality Assurance Specialist
Irvine, CA · On-site
$71K - $85K/yr
... pharmaceutical and biotechnology clients. Why Forma? Unlike large, highly layered organizations ... Requirements Job Overview/Summary The Specialist supports Quality Assurance activities regarding ...
Quality Assurance Specialist
Irvine, CA · On-site
$71K - $85K/yr
... pharmaceutical and biotechnology clients. Why Forma? Unlike large, highly layered organizations ... Requirements Job Overview/Summary The Specialist supports Quality Assurance activities regarding ...
Quick apply
Quality Assurance Specialist
Irvine, CA · On-site
$71K - $85K/yr
... pharmaceutical and biotechnology clients. Why Forma? Unlike large, highly layered organizations ... Requirements Job Overview/Summary The Specialist supports Quality Assurance activities regarding ...
(USA) Specialist, Quality Assurance
Irvine, CA · On-site
$28 - $54/hr
The (USA) Specialist, Quality Assurance is responsible for executing operational analyses to ... pharmaceuticals. By promoting compliance and ethical standards, this position contributes to ...
(USA) Specialist, Quality Assurance
Irvine, CA · On-site
$28 - $54/hr
The (USA) Specialist, Quality Assurance is responsible for executing operational analyses to ... pharmaceuticals. By promoting compliance and ethical standards, this position contributes to ...
(USA) Specialist, Quality Assurance
$28 - $54/hr
The (USA) Specialist, Quality Assurance is responsible for executing operational analyses to ... pharmaceuticals. By promoting compliance and ethical standards, this position contributes to ...
New
(USA) Specialist, Quality Assurance
$28 - $54/hr
The (USA) Specialist, Quality Assurance is responsible for executing operational analyses to ... pharmaceuticals. By promoting compliance and ethical standards, this position contributes to ...
New
Quality Assurance Inspector
Anaheim, CA · On-site
$23 - $25/hr
... QA activities and training · Monitors all aspects of production to assure adherence to cGMP and ... Supplement or Pharmaceutical industry is desirable · Working knowledge of cGMPs · General ...
Quick apply
Quality Assurance Inspector
Anaheim, CA · On-site
$23 - $25/hr
... QA activities and training · Monitors all aspects of production to assure adherence to cGMP and ... Supplement or Pharmaceutical industry is desirable · Working knowledge of cGMPs · General ...
Quality Assurance Inspector
Anaheim, CA · On-site
$23 - $25/hr
... QA activities and training · Monitors all aspects of production to assure adherence to cGMP and ... Supplement or Pharmaceutical industry is desirable · Working knowledge of cGMPs · General ...
Quick apply
Quality Assurance Inspector
Anaheim, CA · On-site
$23 - $25/hr
... QA activities and training · Monitors all aspects of production to assure adherence to cGMP and ... Supplement or Pharmaceutical industry is desirable · Working knowledge of cGMPs · General ...
Associate Manager, Quality Assurance
Irvine, CA · On-site
$118K - $196K/yr
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 ...
Associate Manager, Quality Assurance
Irvine, CA · On-site
$118K - $196K/yr
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 ...
Corporate Quality Assurance Manager
Irvine, CA · On-site
$125K - $160K/yr
... Pharmaceutical, biotechnology, or medical device manufacturing in critical aseptic (sterile) environments, or o Quality Assurance leadership within cleanroom laundry operations. · Demonstrated ...
Quick apply
Corporate Quality Assurance Manager
Irvine, CA · On-site
$125K - $160K/yr
... Pharmaceutical, biotechnology, or medical device manufacturing in critical aseptic (sterile) environments, or o Quality Assurance leadership within cleanroom laundry operations. · Demonstrated ...
As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards ... The Quality Assurance (QA) Operations Supervisor is a critical, hands-on leadership role ...
As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards ... The Quality Assurance (QA) Operations Supervisor is a critical, hands-on leadership role ...
Manager III, Quality Assurance (Product Release) Company ... B. Braun US Pharmaceutical Manufacturing LLC Job Posting Location: Irvine, California, United ...
Manager III, Quality Assurance (Product Release) Company ... B. Braun US Pharmaceutical Manufacturing LLC Job Posting Location: Irvine, California, United ...
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 · 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 ...
The QA Manager partners cross-functionally with Operations, Maintenance, Supply Chain, Product ... S. We operate over 2,200 stores, 1,732 pharmacies, 405 fuel centers, 22 distribution facilities ...
The QA Manager partners cross-functionally with Operations, Maintenance, Supply Chain, Product ... S. We operate over 2,200 stores, 1,732 pharmacies, 405 fuel centers, 22 distribution facilities ...
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 ...
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 ...
Quality Assurance Auditor/Inspector
Corona, CA · On-site
$18 - $23/hr
... the Quality Assurance Auditor/Inspector is primarily responsible for auditing manufacturing ... pharmaceutical industry • Experience with GMP regulations and Good Documentation Practices • ...
Quality Assurance Auditor/Inspector
Corona, CA · On-site
$18 - $23/hr
... the Quality Assurance Auditor/Inspector is primarily responsible for auditing manufacturing ... pharmaceutical industry • Experience with GMP regulations and Good Documentation Practices • ...
Quality Assurance Auditor/Inspector
$18 - $23/hr
... Quality Assurance Auditor/Inspector is primarily responsible for auditing manufacturing ... dietary supplement or pharmaceutical industry Experience with GMP regulations and Good ...
Quality Assurance Auditor/Inspector
$18 - $23/hr
... Quality Assurance Auditor/Inspector is primarily responsible for auditing manufacturing ... dietary supplement or pharmaceutical industry Experience with GMP regulations and Good ...
Pharmaceutical Qa information
See Riverside, CA salary details
$11.29 - $17.19
4% of jobs
$17.19 - $23.10
12% of jobs
$23.10 - $29
7% of jobs
$31.58 is the 25th percentile. Wages below this are outliers.
$29 - $34.90
4% of jobs
$34.90 - $40.81
6% of jobs
$40.81 - $46.71
7% of jobs
The median wage is $50.90 / hr.
$46.71 - $52.62
13% of jobs
$52.62 - $58.52
13% of jobs
$62.58 is the 75th percentile. Wages above this are outliers.
$58.52 - $64.43
13% of jobs
$64.43 - $70.33
15% of jobs
$70.33 - $76.24
6% of jobs
$11
$48
$76
How much do pharmaceutical qa jobs pay per hour?
What is a pharmaceutical QA?
Is pharmaceutical QA a good career?
What is the difference between Pharmaceutical Qa vs Pharmaceutical Quality Control Analyst?
| Aspect | Pharmaceutical Qa | Pharmaceutical Quality Control Analyst |
|---|---|---|
| Certifications | GMP, GDP, ISO certifications | GMP, GLP, ISO certifications |
| Work Environment | Quality assurance departments, regulatory compliance | Laboratories, testing facilities |
| Primary Focus | Ensuring quality processes and compliance | Testing 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?
What are the key skills and qualifications needed to thrive as a pharmaceutical QA, and why are they important?
How to become a pharmaceutical QA?

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.