Job Title: QA Inspector I - 1st Shift FLSA Classification: Full-Time, Non-Exempt/Hourly ... Advanced vocational training or education in pharmaceutical manufacturing, industrial management or ...
Job Title: QA Inspector I - 1st Shift FLSA Classification: Full-Time, Non-Exempt/Hourly ... Advanced vocational training or education in pharmaceutical manufacturing, industrial management or ...
QA Inspector I - 1st Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 1st Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...
QA Inspector I - 1st Shift
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 1st Shift
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 3rd Shift
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 3rd Shift
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 2nd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 2nd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
$23 - $30/hr
Minimum of two(2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...
$23 - $30/hr
Minimum of two(2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 2nd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 2nd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...
$23 - $30/hr
Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...
QA Specialist
Indianapolis, IN · On-site
$21/hr
Indianapolis, IN 46221 | Contract Position About the Role Join a dynamic team as a QA Specialist supporting essential packaging operations in the pharmaceutical industry. This is an opportunity to ...
QA Specialist
Indianapolis, IN · On-site
$21/hr
Indianapolis, IN 46221 | Contract Position About the Role Join a dynamic team as a QA Specialist supporting essential packaging operations in the pharmaceutical industry. This is an opportunity to ...
Executive Director, CMC QA
Novato, CA · On-site
$294.10 - $363.30/hr
Typically 15+ years of progressive experience in pharmaceutical, biotechnology, biologics, gene ... Proven ability to lead CMC QA strategy for rapid development, rare disease, ultrarare disease ...
New
Executive Director, CMC QA
Novato, CA · On-site
$294.10 - $363.30/hr
Typically 15+ years of progressive experience in pharmaceutical, biotechnology, biologics, gene ... Proven ability to lead CMC QA strategy for rapid development, rare disease, ultrarare disease ...
New
Bachelor's degree in a science, engineering, or pharmaceutical-related field of study or equivalent experience. * Minimum 5 years' experience in pharmaceutical leadership with QA experience ...
Bachelor's degree in a science, engineering, or pharmaceutical-related field of study or equivalent experience. * Minimum 5 years' experience in pharmaceutical leadership with QA experience ...
Bachelor's degree in a science, engineering, or pharmaceutical-related field of study or equivalent experience. * Minimum 5 years' experience in pharmaceutical leadership with QA experience ...
Bachelor's degree in a science, engineering, or pharmaceutical-related field of study or equivalent experience. * Minimum 5 years' experience in pharmaceutical leadership with QA experience ...
Q.A. Supervisor
$60K - $72K/yr
Qualified candidates will have the following: * 2 to 5 years of experience in Quality Assurance in food manufacturing, pharmaceuticals, or medical devices. Experience with FDA, GMP standards.
Quick apply
Q.A. Supervisor
$60K - $72K/yr
Qualified candidates will have the following: * 2 to 5 years of experience in Quality Assurance in food manufacturing, pharmaceuticals, or medical devices. Experience with FDA, GMP standards.
Q.A. Supervisor
$60K - $72K/yr
Qualified candidates will have the following: * 2 to 5 years of experience in Quality Assurance in food manufacturing, pharmaceuticals, or medical devices. Experience with FDA, GMP standards.
Quick apply
Q.A. Supervisor
$60K - $72K/yr
Qualified candidates will have the following: * 2 to 5 years of experience in Quality Assurance in food manufacturing, pharmaceuticals, or medical devices. Experience with FDA, GMP standards.
Bachelor's degree in Life Sciences, Pharmacy, or a related health field. * 4+ years of experience in pharmaceutical manufacturing (Packaging and Labelling Operations preferred), quality assurance, or ...
Bachelor's degree in Life Sciences, Pharmacy, or a related health field. * 4+ years of experience in pharmaceutical manufacturing (Packaging and Labelling Operations preferred), quality assurance, or ...
Quality Assurance In Pharmaceutical information
See salary details
$12.98 - $15.76
9% of jobs
$17.41 is the 25th percentile. Wages below this are outliers.
$15.76 - $18.53
28% of jobs
The median wage is $19.87 / hr.
$18.53 - $21.31
29% of jobs
$23.06 is the 75th percentile. Wages above this are outliers.
$21.31 - $24.08
16% of jobs
$24.08 - $26.86
6% of jobs
$26.86 - $29.63
3% of jobs
$29.63 - $32.41
2% of jobs
$32.41 - $35.18
3% of jobs
$35.18 - $37.96
2% of jobs
$37.96 - $40.73
1% of jobs
$40.73 - $43.51
1% of jobs
$12
$23
$43
How much do quality assurance in pharmaceutical jobs pay per hour?
As of Aug 8, 2026, the average hourly pay for quality assurance in pharmaceutical in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.
Is quality assurance a good career in the pharmaceutical industry?
Quality assurance in the pharmaceutical industry is a stable and growing career, focusing on ensuring products meet safety and regulatory standards. It often requires knowledge of Good Manufacturing Practices (GMP), quality control processes, and relevant certifications, making it a vital role for maintaining product integrity and compliance.
What are some common challenges faced by quality assurance professionals in the pharmaceutical industry, and how can they be effectively managed?
Quality Assurance (QA) professionals in the pharmaceutical industry often face challenges such as keeping up with evolving regulatory requirements, ensuring consistent documentation, and coordinating cross-functional teams during audits. Managing these challenges requires continuous training, strong attention to detail, and effective communication skills. Collaboration with other departments, such as production and regulatory affairs, is key to identifying issues early and maintaining compliance with Good Manufacturing Practices (GMP). Establishing clear quality procedures and staying proactive with process improvements also help QA professionals maintain high standards and reduce risks.
What are the key skills and qualifications needed to thrive as a quality assurance professional in the pharmaceutical industry?
A successful Quality Assurance professional in pharmaceuticals needs a solid background in life sciences or pharmacy, understanding of GMP regulations, and relevant QA experience. Familiarity with quality management systems (QMS), documentation software, and regulatory compliance tools is typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for excelling in this role. These skills ensure product safety, regulatory compliance, and the consistent delivery of high-quality pharmaceutical products.
What does quality assurance do in the pharmaceutical industry?
Quality assurance professionals in the pharmaceutical industry ensure that products meet safety, quality, and regulatory standards throughout the manufacturing process. They develop and implement procedures, conduct audits, and review documentation to prevent defects and ensure compliance with Good Manufacturing Practices (GMP).
What does a quality assurance professional do in the pharmaceutical industry?
A Quality Assurance (QA) professional in the pharmaceutical industry is responsible for ensuring that all products meet established standards of quality, safety, and efficacy. They develop, maintain, and monitor procedures and systems that comply with regulatory requirements such as Good Manufacturing Practices (GMP). QA professionals conduct audits, review documentation, manage deviations, and support continuous improvement to ensure that medications are safe for patients. Their work is critical in preventing errors, ensuring product consistency, and maintaining the trust of regulatory agencies and consumers.
What is the difference between Quality Assurance In Pharmaceutical vs Quality Control In Pharmaceutical?
| Aspect | Quality Assurance In Pharmaceutical | Quality Control In Pharmaceutical |
|---|---|---|
| Focus | Processes, compliance, and preventing defects | Testing and inspecting products for defects |
| Responsibilities | Developing quality systems, audits, documentation | Sampling, testing, and analyzing products |
| Credentials | GMP certifications, quality management training | Lab certifications, analytical testing skills |
| Work Environment | Office-based, quality departments, manufacturing sites | Laboratories, manufacturing facilities |
Quality Assurance In Pharmaceutical focuses on establishing and maintaining quality systems to prevent issues, while Quality Control In Pharmaceutical emphasizes testing products to identify defects. Both roles are essential in ensuring pharmaceutical safety and compliance, but they differ in scope and daily tasks.
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Job description
Job Title: QA Inspector I - 1st Shift FLSA Classification: Full-Time, Non-Exempt/Hourly Professional Work Location: Fall River, MAWork Hours: First Shift: 7:00AM - 3:30PM (May vary based on business needs)Reports To: Quality Assurance Manager PURPOSEThe purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs).JOB DESCRIPTION The Quality Assurance (QA) Inspector position is an individual contributor role and a member of the Plant Quality Team. The position reports to the Manager of QA and may be matrixed to other functional leaders within the Quality or other departments. The essential and typically expected job duties for this position include but are not limited to the following:Perform in-process testing (e.g., weight, thickness, hardness, disintegration, friability, etc.) as per manufacturing batch record instructions.Conduct room and equipment checks (where applicable) prior to each stage of manufacturing by following detailed written procedures.Execute acceptable quality limit (AQL) sampling and inspections as required.Inspect in-process and finished product samples (where applicable) for the Quality Control (QC) Lab and follow detailed documentation procedures to deliver the results to the QC Lab.Maintain records of standard weights and perform daily verification of balances.Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record.Monitor facility and product environmental operating conditions.Review of engineering records such as temperature and humidity data calibration and PM records, Pest control records and contractor related functions.Assess online batch records in terms of completeness of signatures, entries, and actual reconciliation / yields prior to initiation of next processing step.Verify the functionality of all the equipment and associated controls during the batch run.Perform applicable testing and prepare reports for customer complaints.Identify and report any non-conformances and/or discrepancies to management if applicable.Complete other duties or participate in project work as assigned by management. EDUCATION AND EXPERIENCE QUALIFICATIONSMinimum high school diploma.Advanced vocational training or education in pharmaceutical manufacturing, industrial management or related field of study from an accredited college/university is preferred.Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment.Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIESProficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP, and other business applications.Must be able to influence decision-making and facilitate completion of work toward the achievement of the business plan and goals.Effective interpersonal relationship skills and the ability to work in a team environment.Proficiency in the English language to include usage, spelling, grammar and punctuation.Must have current Good Manufacturing Practices (cGMP) knowledge.Must have strong attention-to-detail.Must be a self-starter and demonstrate initiative with seeking additional training or direction as needed.Must have strong organization and communication skills (written, verbal, and presentation).Must be detail-oriented with the ability to multitask and prioritize tasks with strict deadlines.#INDQU Salary: . Date posted: 07/28/2026