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Quality Control Associate Jobs in Stratford, CT (NOW HIRING)

Advatix

Temporary Warehouse Associate

Islandia, NY · On-site

$17/hr

Fulfillment Center Operations Associate Role Description XPDEL is looking for a Fulfillment Center ... Quality control inspection of products Skills and Qualifications * Detail-oriented, reliable ...

Advatix, Inc.

Temporary Warehouse Associate

Islandia, NY · On-site

$17/hr

Fulfillment Center Operations Associate Role Description XPDEL is looking for a Fulfillment Center ... Quality control inspection of products Skills and Qualifications * Detail-oriented, reliable ...

GW Lisk Company Inc

Quality Inspector

Hauppauge, NY · On-site

$20 - $30/hr

Understand the non-conforming material process to ensure control of material. * Work and ... Associates or higher in Technical Discipline/Trade preferred * Minimum 3 years in a precision ...

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Quality Control Associate information

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$11

$26

$39

How much do quality control associate jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for quality control associate in Stratford, CT is $26.36, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $32.12 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in Stratford, CT?

The most popular types of Quality Control jobs in Stratford, CT are:

What cities near Stratford, CT are hiring for Quality Control Associate jobs?

Cities near Stratford, CT with the most Quality Control Associate job openings:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Stratford, CT as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $54,839 per year, or $26.4 per hour.

QC Environmental Monitoring Technician I (11pm-7:30am)

American Regent, Inc.

Shirley, NY • On-site

$23.61 - $25/hr

Full-time

Medical, Life, Retirement, PTO

Posted 26 days ago

American Regent rating

7.2

Company rating: 7.2 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

70th of 86 rated pharmaceutical

Job description

Nature and Scope
The Environmental Monitoring Team is responsible for the activities associated with the manufacture of safe, effective, and sterile pharmaceuticals in accordance with company SOPs, policies, and cGMPs. The Environmental Monitoring Team works in concert with the manufacturing department and plays a critical role in ensuring environmental control of the aseptic manufacturing facility. The EMT I position is primarily responsible for performing environmental monitoring activities including sample collection of water, air (viable and non-viable), compressed gas, surfaces, and personnel within the classified areas of the manufacturing facility.
Essential Duties and Responsibilities
Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time.
  • Ensure all work is performed and documented in accordance with existing company policies, procedures, Current Good Manufacturing Practices, and health and safety requirements.
  • Manage assigned daily workload to meet requirements and perform sampling as per the schedule.
  • Must complete and maintain gowning qualifications for support areas as well as the Aseptic Processing Area to work in clean rooms.
  • Perform environmental monitoring activities including sampling of air (Viable and Non-viable), compressed air and nitrogen, surface, and personnel inside the classified manufacturing areas.
  • Conduct water sampling throughout facility.
  • Complete incubation, transfer and final reading of samples if needed.
  • Record results and report deviations as per specifications.
  • Capture sampling life cycles in the LIMS software and assist with data entry for retrieval and trending from Labware LIMS.
  • Maintain accurate records of work performed in Labware LIMS and Laboratory documentation systems according to Good Documentation Practices, Standard Operating Procedures (SOPs) and policies.
  • Maintains compliance with all required SOPs and policies.
  • Communicate any discrepancies or deviations to supervision/management upon discovery.
  • Author or help data collection for assigned investigation report related to EM/PM events.
  • Perform clean room behavior and area assessments as per procedures if needed.
  • Review environmental and personnel monitoring sample results in Labware LIMS if needed.
  • Input data/results into database and conduct trend analysis.
  • Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.
  • High School Diploma or GED equivalent required. Associate degree in microbiology, biology or related scientific field preferred.
  • One year experience in academic or industry work experience in laboratory setting or manufacturing with focus on microbiology preferred.
  • Knowledge of aseptic technique preferred.
  • Must be able to maintain APA gown qualification for EM support.
  • Ability to perform basic mathematical calculations.
  • Ability to work independently and as a team with minimal supervision.
  • Organization and attention to detail.
  • Excellent communication skills (Oral and Written).
  • Working knowledge of MS-Office software and PC Skills Required.
  • Good work ethic and highly motivated.
  • Good time-management skills.
  • Ability to work in a fast-paced environment.
  • Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals.
  • Ability to work overtime, weekend and holidays as needed.

Physical Environment and Requirements
  • Physically able to wear and aseptically don cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE is essential for the health and safety of employees.
  • Employees must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly.
  • Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision.
  • Employee must be able to occasionally lift and/or move up to 25 pounds.
  • Job activities require long periods of standing and use of controlled movements as well as aseptic techniques/behaviors in the sterile filling suites.

Expected hourly range:
$23.61 - $25.00
The hourly range displayed is the minimum and maximum hourly rate for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role. Actual compensation for the role will be based on a number of different factors including but not limited to the candidate's qualifications, education, knowledge, skills and experience.
American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits.
American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.
Applicants have rights under Federal Employment Laws.
  • FMLA poster: https://www.dol.gov/whd/regs/compliance/posters/fmlaen.pdf
  • Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov)
  • Employee Polygraph Protection Act: https://www.dol.gov/whd/regs/compliance/posters/eppac.pdf

Alert: We're aware of individuals impersonating our staff to target job seekers. Please note:
• All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.
• Our recruiting process includes multiple in person and/or video interviews and assessments.
• If you are unsure about the legitimacy of a message, contact John Rossini at jrossini@americanregent.com before responding.
• We never request payment, bank information, or personal financial details during our offer process.
Your security is important to us, and we encourage you to stay vigilant when job searching.
American Regent Inc. endeavors to make https://careers.americanregent.com/ accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email hrtalentacquisition@americanregent.com.

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