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Senior Quality Assurance Associate About Us: Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility, enabling us to meet the needs of our patients and prescribers through a ...
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Be Seen First
Senior Quality Assurance Associate About Us: Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility, enabling us to meet the needs of our patients and prescribers through a ...
Quick apply
Be Seen First
Senior Quality Assurance Associate About Us: Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility, enabling us to meet the needs of our patients and prescribers through a ...
The Senior QA Associate is an individual contributor with no direct reports. Senior QA Associate receives no instruction on routine work as these asks are described in detail in established ...
The Senior QA Associate is an individual contributor with no direct reports. Senior QA Associate receives no instruction on routine work as these asks are described in detail in established ...
San Diego, CA · On-site
$30 - $33/hr
We're looking for a Senior Quality Assurance Associate who enjoys being close to the product, the process, and the people. In this role, you'll be a key contributor to ensuring our finished goods ...
San Diego, CA · On-site
$30 - $33/hr
We're looking for a Senior Quality Assurance Associate who enjoys being close to the product, the process, and the people. In this role, you'll be a key contributor to ensuring our finished goods ...
Cincinnati, OH · On-site
The position will perform QA work responsibilities in support of manufacturing and facility operations, including quality systems and projects. Functions include proactive support of change control ...
Cincinnati, OH · On-site
The position will perform QA work responsibilities in support of manufacturing and facility operations, including quality systems and projects. Functions include proactive support of change control ...
Third Party Quality Senior Associate The Third Party Quality Senior Associate will be responsible for the review and disposition of batch record documentation for Alora distributed products ...
Third Party Quality Senior Associate The Third Party Quality Senior Associate will be responsible for the review and disposition of batch record documentation for Alora distributed products ...
The position will perform QA work responsibilities in support of manufacturing and facility operations, including quality systems and projects. Functions include proactive support of change control ...
The position will perform QA work responsibilities in support of manufacturing and facility operations, including quality systems and projects. Functions include proactive support of change control ...
Paulsboro, NJ · On-site
$90K - $115K/yr
A minimum of 5 years in QA/QC/Compliance in an FDA/DEA regulated environment or a minimum of 5-7 years in API manufacturing in an FDA/DEA regulated environment is desired. * The ability to exercise ...
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Paulsboro, NJ · On-site
$90K - $115K/yr
A minimum of 5 years in QA/QC/Compliance in an FDA/DEA regulated environment or a minimum of 5-7 years in API manufacturing in an FDA/DEA regulated environment is desired. * The ability to exercise ...
Apply Early
Toano, VA · On-site
$17 - $19/hr
QUALITY ASSURANCE ASSOCIATES IN TOANO, VA! Position: Quality Assurance Associate Pay: $17.00 - $19.00 per hour (DOE) Schedule: Monday - Friday, 8:00 AM - 5:00 PM Some weekends required Benefits:
Toano, VA · On-site
$17 - $19/hr
QUALITY ASSURANCE ASSOCIATES IN TOANO, VA! Position: Quality Assurance Associate Pay: $17.00 - $19.00 per hour (DOE) Schedule: Monday - Friday, 8:00 AM - 5:00 PM Some weekends required Benefits:
$17 - $19/hr
QUALITY ASSURANCE ASSOCIATES IN TOANO, VA! Position: Quality Assurance Associate Pay: $17.00 - $19.00 per hour (DOE) Schedule: Monday - Friday, 8:00 AM - 5:00 PM Some weekends required Benefits:
Quick apply
Apply Early
$17 - $19/hr
QUALITY ASSURANCE ASSOCIATES IN TOANO, VA! Position: Quality Assurance Associate Pay: $17.00 - $19.00 per hour (DOE) Schedule: Monday - Friday, 8:00 AM - 5:00 PM Some weekends required Benefits:
Apply Early
Sheboygan Falls, WI · On-site
$26 - $46/hr
Duties will be focused on quality system development and maintenance activities, including supplier and material qualification, approval and change management. Who You Are: Minimum Qualifications:
Sheboygan Falls, WI · On-site
$26 - $46/hr
Duties will be focused on quality system development and maintenance activities, including supplier and material qualification, approval and change management. Who You Are: Minimum Qualifications:
Fishers, IN · On-site
The QA Associate will need to provide support with identifying operational and quality gaps. The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing ...
Fishers, IN · On-site
The QA Associate will need to provide support with identifying operational and quality gaps. The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing ...
Bristol, PA · On-site
The Senior Associate, QA Operations is responsible for providing quality oversight of GMP manufacturing and development activities through direct quality presence on the manufacturing floor and ...
Bristol, PA · On-site
The Senior Associate, QA Operations is responsible for providing quality oversight of GMP manufacturing and development activities through direct quality presence on the manufacturing floor and ...
$20.45 - $24.92/hr
We are currently seeking a Quality Assurance Associate to join our team on Second Shift . Shift times run Monday - Thursday from 3:00pm - 1:20 am. Reporting to the QA Coordinator, the Quality ...
$20.45 - $24.92/hr
We are currently seeking a Quality Assurance Associate to join our team on Second Shift . Shift times run Monday - Thursday from 3:00pm - 1:20 am. Reporting to the QA Coordinator, the Quality ...
Sheboygan Falls, WI · On-site
$26 - $46/hr
Duties will be focused on quality system development and maintenance activities, including supplier and material qualification, approval and change management. Who You Are: Minimum Qualifications:
Sheboygan Falls, WI · On-site
$26 - $46/hr
Duties will be focused on quality system development and maintenance activities, including supplier and material qualification, approval and change management. Who You Are: Minimum Qualifications:
Sheboygan Falls, WI · On-site
$46/hr
Duties will be focused on quality system development and maintenance activities, including supplier and material qualification, approval and change management. Who You Are: Minimum Qualifications:
Sheboygan Falls, WI · On-site
$46/hr
Duties will be focused on quality system development and maintenance activities, including supplier and material qualification, approval and change management. Who You Are: Minimum Qualifications:
Quality Assurance Associate works under the supervision of the Quality Management Representative or their designee and is responsible for ensuring compliance to the requirements of the corporate ...
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Quality Assurance Associate works under the supervision of the Quality Management Representative or their designee and is responsible for ensuring compliance to the requirements of the corporate ...
Columbia, SC · On-site
$26.60/hr
The Quality Assurance Associate II is responsible for maintaining all training of a QAA I in addition to the review of controlled documents (both executed and unexecuted) in accordance with ...
Columbia, SC · On-site
$26.60/hr
The Quality Assurance Associate II is responsible for maintaining all training of a QAA I in addition to the review of controlled documents (both executed and unexecuted) in accordance with ...
Quality Assurance Associate Location: Onsite - Henderson, NV Salary: $50,700 and eligible for over time About PSI Join Us at PSI - Where You Belong, Grow, and Thrive! At PSI, we believe that ...
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Quality Assurance Associate Location: Onsite - Henderson, NV Salary: $50,700 and eligible for over time About PSI Join Us at PSI - Where You Belong, Grow, and Thrive! At PSI, we believe that ...
Winchester, KY · On-site
$21 - $22.94/hr
Manage quality status of WIP and finished good materials on physical inventory and in inventory system (JD Edwards) Other assignments as needed within the scope of QA Associate training curriculum ...
Winchester, KY · On-site
$21 - $22.94/hr
Manage quality status of WIP and finished good materials on physical inventory and in inventory system (JD Edwards) Other assignments as needed within the scope of QA Associate training curriculum ...
Augusta, GA · On-site
Quality Assurance Associate Location: Augusta, GA, 30901 Position Overview We are seeking a detail-oriented and proactive Quality Assurance Associate to join our team in Augusta, GA. The ideal ...
Augusta, GA · On-site
Quality Assurance Associate Location: Augusta, GA, 30901 Position Overview We are seeking a detail-oriented and proactive Quality Assurance Associate to join our team in Augusta, GA. The ideal ...
$29K - $38.5K
17% of jobs
$44.1K is the 25th percentile. Wages below this are outliers.
$38.5K - $47.9K
14% of jobs
$47.9K - $57.4K
4% of jobs
$57.4K - $66.8K
14% of jobs
The median wage is $68.1K / yr.
$66.8K - $76.3K
12% of jobs
$76.3K - $85.7K
9% of jobs
$90.7K is the 75th percentile. Wages above this are outliers.
$85.7K - $95.2K
11% of jobs
$95.2K - $104.6K
9% of jobs
$104.6K - $114.1K
6% of jobs
$114.1K - $123.5K
3% of jobs
$123.5K - $133K
1% of jobs
$29K
$74.2K
$133K
| Aspect | Senior Qa Associate | Quality Assurance Tester |
|---|---|---|
| Required Credentials | Bachelor's degree in Computer Science or related field; experience in QA | High school diploma or equivalent; some technical training or certifications preferred |
| Work Environment | Collaborates with cross-functional teams; involved in planning and oversight | Primarily executes test cases; reports bugs and issues |
| Employer & Industry Usage | Used in software development, technology companies, and IT services | Common in software firms, startups, and quality-focused organizations |
| Search & Comparison Intent | Often compared for experience level and responsibilities | Compared for entry-level or mid-level QA roles |
The Senior Qa Associate typically has more experience, responsibilities in planning, and oversight in quality assurance processes, whereas a Quality Assurance Tester focuses on executing tests and identifying bugs. The senior role often involves collaboration with development teams and strategic planning, making it suitable for professionals with more experience in QA.

Full-time
Medical, Dental, Vision, Retirement
Posted 14 days ago
Leads internal and external audits and participates in external audits involving regulatory agencies.
Coordinates with production to write and review GMP documents including standard operating procedures, protocols, risk assessments, and reports.
Oversees complaint intake process and assists production with completing complaints, investigations, and deviations.
Senior Quality Assurance Associate
About Us:
Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility, enabling us to meet the needs of our patients and prescribers through a variety of office use products including but not limited to injectables, pellets, and topicals. Being a member of the Carie Boyd team means prioritizing patient needs, dedication to quality, and the drive to continue to scale our innovative business in new and diverse ways.
Job Description
The Senior Quality Assurance Associate provides guidance on interpretation of regulatory requirements, leads internal and external audits, and coordinates with production to write and review GMP documents.
Responsibilities
· Under the direction of the Quality Director, the Senior QA Associate will assist with the overall development, implementation, and management of the Quality Management System (QMS)
· Coordinates with production to write standard operating procedures, protocols, risk assessments, reports, and other GMP documents
· Ensures standard operating procedures are written and implemented in compliance with the company’s policies, government regulations, and industry best practices
· Oversees complaint intake process, and assists production with completing complaints, investigations, and deviations in a timely manner
· Writes Annual Product Review (APR) reports and ensures maintenance to established review periods
· Creates raw material and finished product specifications, ensuring adherence to USP/NF Monographs and other regulatory requirements
· Performs risk assessments and vendor evaluation activities as part of Vendor Qualification
· Performs internal/external audits and participates in external audits involving regulatory agencies
· Evaluates and recommends alternative auditing procedures for continuous improvement
· Performs GMP document review, as needed
· Assist Quality Management with other QA duties, as needed
Qualifications:
· Bachelor’s degree or higher in a life science or related discipline or 4 + years in GMP pharmaceutical manufacturing, 503b outsourcing facility, or cosmetic manufacturing.
· Strong working knowledge of cGMP and GDP
· 2 or more years of experience with technical writing
· Strong documentation skills
Confidentiality
The employee must maintain the confidentiality of company information and, pursuant to State and Federal Law (including the Health Insurance Portability and Accountability (HIPAA) Act of 1996), protected health information.
EOE/ADA
Carie Boyd Pharmaceuticals is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, Carie Boyd Pharmaceuticals will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer.
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Health care and social assistance
11 - 50 Employees
Hurst, TX, US
1965