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Quality Control Associate Jobs in Connecticut (NOW HIRING)

Boeing

Associate Quality Inspector

Enfield, CT · On-site

$41K - $58K/yr

Associate Quality Inspector Company: Boeing Distribution, Inc. Boeing Global Services (BGS ... Disposition and control of on-conforming products. Basic Qualifications (Required Skills/Experience ...

Boeing

Associate Quality Inspector

Enfield, CT · On-site

$41K - $58K/yr

Associate Quality Inspector Company: Boeing Distribution, Inc. Boeing Global Services (BGS ... Disposition and control of on-conforming products. Basic Qualifications (Required Skills/Experience ...

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Quality Control Associate information

See Connecticut salary details

$10

$24

$36

How much do quality control associate jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for quality control associate in Connecticut is $24.22, according to ZipRecruiter salary data. Most workers in this role earn between $17.60 and $29.52 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, and why are they important?

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.

Which is higher position, QA or QC?

In the context of a Quality Control Associate role, Quality Assurance (QA) is generally considered a higher-level function that focuses on preventing defects through process improvements, while Quality Control (QC) involves inspecting products to identify defects. QA roles often involve more strategic responsibilities and may require broader skills or certifications, whereas QC is more about testing and inspection tasks. The hierarchy can vary by organization, but QA typically holds a higher or more senior position than QC.

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 Connecticut? The most popular types of Quality Control jobs in Connecticut are:
What are popular job titles related to Quality Control Associate jobs in Connecticut? For Quality Control Associate jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Quality Control Associate jobs in Connecticut look for? The top searched job categories for Quality Control Associate jobs in Connecticut are:
What cities in Connecticut are hiring for Quality Control Associate jobs? Cities in Connecticut with the most Quality Control Associate job openings:
What are popular job titles related to Quality Control Associate jobs in CT? For Quality Control Associate jobs in CT, the most frequently searched job titles are:
Quality Control Associate jobs near you
Associate Director, Analytical Development and Clinical QC

Associate Director, Analytical Development and Clinical QC

Alexion Pharmaceuticals

New Haven, CT • On-site

Full-time

Posted 10 days ago

Job description

This position will play a key leadership role in Alexion's Late Stage Analytical team, which requires analytical expertise and proven success in management of development projects through the CMC lifecycle. This position will lead multiple projects in parallel and working closely with other PDCS teams, Regulatory, QA and external QC laboratories as a lead to designing the strategy of late-stage analytical activities including method transfer/validation, compendia method verification, and overall testing strategy throughout all phases of the product lifecycle. Moreover, this position will lead to authoring regulatory filing in relevant analytical sections with a focused understanding of country-specific requirements!
You will be responsible for:
  • Leading all aspects of analytical method validation, transfers, and compendia method verifications across all stages of clinical development and method life-cycle stages
  • Analytical lead for CMC programs, emphasizing late-stage programs, which may be internal or external with cross functional collaboration.
  • Analytical end-to-end strategy for key late-stage biologics programs including analytical control strategy, method lifecycle and QC testing supervision, problem resolution and inquiries, and key BLA/commercial analytical
  • Supervision of analytical QC testing, problem-solving, and data analysis are conducted for the CMC program. This provides oversight of the analytical program's health. It also helps identify potential analytical and program risks early.
  • Leading independently regulatory authoring for both medical and market-facing submissions for all markets including responses to health authority queries and requests for information

You will need to have:
  • Advanced degree (PhD or MSc) in Biochemistry, Analytical Chemistry, Molecular Biology, Pharmaceutical Sciences, or related field with 8-12+ years of progressive experience in biologics analytical development across clinical and commercial stages
  • Validated first-hand expert knowledge and technical proficiency with monoclonal antibodies, bispecifics, fusion proteins.
  • Technical expertise in chromatography (e.g., SEC, RP, IEX), capillary electrophoresis (CE-SDS, cIEF), spectroscopy (UV/Vis, fluorescence, CD), bioassays (binding, potency), and residuals/impurities testing (HCP, DNA, residual Protein A)
  • Compendia method experience emphasizing USP, EP and JP compliance
  • Strong written and verbal skills for clear reports, regulatory submissions, and presentations to technical and non-technical collaborators
  • Demonstrated success in method development, qualification/validation (per ICH Q2), transfer to QC/CMOs, and continued verification for commercial control strategies.
  • Strong command of ICH (Q5E, Q6B, Q8-Q12), USP/EP, FDA/EMA expectations for biologics, GMP/GLP compliance, and authoring/reviewing CTD Module 3, IND/IMPD, BLA/MAA analytical sections and responses to agency queries.
  • Proficiency with GxP compliant documentation, ALCOA+ data integrity principles, OOS/OOT handling, deviation/CAPA management, and audit readiness
  • Ability to define critical quality attributes (CQAs), build specifications, and implement control approaches aligned with Quality by Build (QbB)

We would prefer you to have:
  • Experience in microbiology assays (e.g., required day of harvest, bioburden, endotoxin, sterility, and CCIT)
  • Background in analytical method development and sound scientific understanding of Critical Quality Attributes/QbD/DOE principles as well as statistical data analysis and relevant tools
  • Experience leading all aspects of CDMO/CRO analytical activities including routine testing oversight, troubleshooting and investigations and method qualification, validation, and transfer.
  • Experience in country specific compendia requirements and knowledge of CHP
  • Experience leading ICH stability programs (Q1), shelf-life modeling, and projections and related statistical approaches.
  • Experience in extended characterization and comparability including forced degradation studies for process comparability.
  • Familiarity with LIMS, ELN, Chromatography Data Systems, data visualization, and automation/robotics in analytical workflows
  • Expertise with AI tools and statistical software, for example JMP
  • Track record of building, mentoring, and developing high-performing teams; resource planning, and performance management

The duties of this role are generally conducted in a lab environment. As is typical of a lab-based role, employees will work comfortably in a controlled environment with and around biological, infectious, and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.
When we put unexpected teams in the same room, we ignite ambitious thinking with the power to encourage life-changing medicines! In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.
Join us in our outstanding and ambitious world.
Why AstraZeneca:
Here, courage, curiosity, and collaboration fuel a relentless focus on transforming cancer outcomes, powered by a pipeline that fuses cutting-edge science with advanced technology. You will work in an environment where unexpected teams come together to spark bold ideas, backed by meaningful investment and a clear path from discovery to impact. We value kindness alongside ambition, and we empower leaders at every level to ask sharp questions, take smart risks, and turn data into decisions that help patients sooner.
Date Posted
01-May-2026
Closing Date
30-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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