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How much do commercial assurance associate jobs pay per year?

As of Sep 14, 2026, the average yearly pay for commercial assurance associate in the United States is $75,617.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $85,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Commercial Assurance Associate job openings in the United States as of July 2026, with employment types broken down into 70% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $75,617 per year, or $36.4 per hour.

Sr.Quality Assurance Associate

Baltimore, MD โ€ข On-site

Artech Information System LLC
Recruiting and Staffing Servicesย โ€ขย 10K+ employees

Contractor

Re-posted 3 days ago


Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

The position is critical to ensuring that Organizational, Site, and Departmental objectives and goals such as Uninterrupted Supply of Product and a Responsive Supply Chain are obtained.

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 procedures and standards.

Receives general instructions on new assignments.

Provides an independent compliance review of their peer s work prior to final management approval.

May work on problems and investigations of diverse scope where they exercise judgment within generally defined practices and policies, knowledge of CGMP, job-related experience.

They independently determine whether the product manufactured by Client meets standards and is acceptable for distribution to Client patients.

The Senior QA Associate is expected to perform their core job functions with minimal supervision and input from management.

Reviews executed commercial production records in a timely manner, ensuring that records are in compliance with GMP s and standard operating procedures.

Upon completion of review, assigns the appropriate disposition.

Functions as a subject matter expert for the QA department.

Represents QA on cross-functional department teams and serves as group leader in the absence of department manager.

Conducts, writes and performs risk assessments for investigations/deviations in collaboration with the production unit to fully understand the impact of any deviation.

With assistance from the production unit, determines root cause and assigns appropriate CAPA.

Product Complaints Contacts customers, conducts and writes investigation, trends complaints, collaborates with the production unit to fully understand the impact of the complaint, and with assistance from production unit determines/assigns appropriate CAPA Drafts or contributes to QA documentation, including investigation reports, standard operating procedures, and annual product reviews (APR)/product quality reviews (PQR). Trends Quality data.

Other duties as assigned to facilitate ongoing Client Baltimore/Gliadel production and/or operational activities including, but not limited to involving Client-Baltimore, ECL, and external partners and companies

Review Out Of Calibration report, weekly alarm trends and Labeling change controls.

Executes AQL inspections and sampling Performs Area Clearance and In Process inspections to support Gliadel production

Periodically summarizes status and progress of assigned activities as requested by supervisor.


Qualifications

BS/BA or MS in Chemistry, or closely related field required.

8+ years of senior level experience in Quality Assurance within the pharmaceutical or closely related industry. Prior supervisory experience preferred, but not required.

Demonstrated experience performing batch record review and disposition, investigating product complaints and conducting deviation investigations.

In depth knowledge of CGMPs and Regulatory Guidelines.

Strong interpersonal and communications skills (oral and written) required.

Demonstrated excellent customer service skills in dealing with external clients.

Demonstrated organizational skills.

Critical thinking and effective decision making skills with ability to identify issues requiring further attention, and ability to initiate and facilitate resolution of those issues in a timely & professional manner.

Strong attention to detail.


Additional Information

This is a time sensitive and critical position a quick response would be of great help.
Contact Information:
Sneha Shrivastava
Technical Recrutier
(973) 967 3348


Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992