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Qc Associate Jobs in Rhode Island (NOW HIRING)

Summary The Quality Associate supports both quality assurance and quality control initiatives regarding Production and Operations to ensure that customer requirements are met, and any discrepancies ...

The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards ...

Associate degree, technical training, or quality related coursework in a related field preferred. * Experience in quality, manufacturing, engineering, inspection, or document control role required.

Quality Technician

Bristol, RI · On-site

$18.75 - $25.25/hr

... control across the S6 and S12 product lines. Executes inspection plans, contains and documents ... associate degree or technical certificate a plus Preferred Skills * Experience in start-up ...

Vault Associate Location: North Kingstown, RI Type: Contract Compensation: Pay Rate $19.00 ... Perform ongoing inspection and quality control to ensure client product accuracy * Maintain the ...

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Qc Associate information

See Rhode Island salary details

$11

$24

$37

How much do qc associate jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for qc associate in Rhode Island is $24.94, according to ZipRecruiter salary data. Most workers in this role earn between $18.12 and $30.38 per hour, depending on experience, location, and employer.

What skills and qualifications are needed to be a QC associate?

To thrive as a QC Associate, you need a background in chemistry, biology, or a related scientific field, often supported by a relevant degree or laboratory experience. Familiarity with laboratory equipment, analytical instruments (like HPLC or GC), and quality management systems (such as GMP or ISO standards) is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring accuracy and collaborating with team members. These competencies are essential for maintaining product quality, regulatory compliance, and operational efficiency in quality control environments.

What is a QC associate?

A QC (Quality Control) Associate is a professional responsible for performing tests and inspections on products, materials, or processes to ensure they meet established quality standards. They work primarily in manufacturing, pharmaceutical, biotechnology, or food industries, helping to identify defects and maintain compliance with regulatory requirements. QC Associates document their findings, report issues, and may assist in implementing corrective actions to improve product quality. Their work is critical in ensuring that only safe and effective products reach customers.

What challenges do QC associates face when ensuring product quality, and how can they be addressed?

QC Associates often encounter challenges such as tight production deadlines, handling multiple testing protocols, and maintaining accuracy under pressure. Adapting to new technologies or updated regulatory standards can also present difficulties. To address these, strong organizational skills, continuous training, and effective communication with cross-functional teams are essential. Additionally, maintaining thorough documentation and proactively identifying potential issues can help ensure consistent product quality and compliance.
What are the most commonly searched types of Qc jobs in Rhode Island? The most popular types of Qc jobs in Rhode Island are:
What are popular job titles related to Qc Associate jobs in Rhode Island? For Qc Associate jobs in Rhode Island, the most frequently searched job titles are:
What cities in Rhode Island are hiring for Qc Associate jobs? Cities in Rhode Island with the most Qc Associate job openings:
Infographic showing various Qc Associate job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $51,867 per year, or $24.9 per hour.

Quality Control Senior Associate

Aequor

West Greenwich, RI

Full-time

Posted 6 hours ago

Posted today


Job description

100% Onsite - Rhode Island Urgent backfill of AMAGJP00015468 (scrubbed resume attached) Urgent role shortlisting EOD Tuesday 7/28 Standard 8-5 local hours The role will be on-site based out of *** Rhode Island and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing the following: in-process, release and stability samples. The laboratory employs a variety of test methodologies that use sophisticated equipment including: HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing.Responsibilities include the following: • Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements • Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks • Ensures that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations • Operate laboratory equipment and instrumentation • Performs review and approval of assays, documents and records • Supports Continual Improvement initiatives • Alerts management of quality, compliance, supply and safety risks • Participate in laboratory investigations • Perform general laboratory housekeeping activities • Completes required assigned training to permit carry through of required tasks • Performs additional duties as specified by managementPreferred Qualifications • 1-2 years' experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing • Demonstrated experience in laboratory investigations, method validation, audits, QC processes • Proven ability to interpret scientific data • Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction Salary: . Date posted: 08/12/2026