Top 6 Quality assurance engineer iii Jobs in Connecticut

Senior Quality Assurance Scientist
Beacon Hill Staffing Group —Mansfield, CT
- $40 - $46 an hour
- Full-time
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Dental insurance
- Vision insurance
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5d
Senior Quality Engineer
Medtronic —North Haven, CT
- $98,400 - $147,600 a year
- Full-time
- Office
- Master's degree
- Bachelor's degree
- Health savings account
- Employee stock purchase plan
Microbiology Analyst III
Millstone Medical Outsourcing —Bloomfield, CT
- $30 - $34 an hour
- Full-time
- Background check
- 5 years
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
8d
Magnetic Particle Inspector level 3
Element Materials Technology —South Windsor, CT
- $70,000 - $85,000 a year
- Mid-level
- High school diploma or GED
- Associate's degree
NDT Responsible Level III/ Department Manager
Element Materials Technology —Enfield, CT
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
2d
Contractor – Nuclear Quality Engineer (NQA-1) – 2008, 2009, and 2022
Johnson Service Group Inc. —United States
- Contract
- Remote
- 5 years
- US work authorization
- Senior level
- Disability insurance
- Health insurance
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Senior Quality Engineer
Deringer-Ney Inc. —Bloomfield, CT
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QA Specialist_QA Engineer (local candidates only)
Millstone Medical Outsourcing —Bloomfield, CT
Support the collection, analysis, and trending of quality metrics. Own and manage assigned CAPAs and change controls, as assigned, though timely completion and…
$85,000 - $105,000 a year
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10d

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Senior Quality Assurance Scientist

Beacon Hill Staffing Group -
Mansfield, CT

Quick Apply

Job Details

Full-time | Contract
$40 - $46 an hour
5 days ago

Benefits

Dental insurance
Vision insurance

Qualifications

Defect resolution root cause analysis
Document control experience within pharmaceutical industry
ICH Q7
Drug regulation
FDA 21 CFR Part 11
GMP
Technical report writing
ICH Q9
Production validation processes
Bachelor's degree
Compliance documentation
ICH Q10
Regulatory/legal compliance standards in production
Biomedical regulatory compliance
Technical writing quality assurance
Test validation method
Standard operating procedures (SOPs)
Standard operating procedures drafting
Failure analysis

Full Job Description

Position Summary

We are seeking a highly skilled and experienced Senior Quality Assurance (QA) Scientist to join our client's team. In this senior-level role, you will be a key driver of product quality, regulatory compliance, and continuous improvement initiatives across the organization. You will apply deep technical expertise to design and execute quality systems and serve as a cross-functional quality partner to R&D, manufacturing, and regulatory affairs.

Key Responsibilities

Quality Systems & Compliance

Design, implement, and maintain comprehensive Quality Management Systems (QMS) in accordance with applicable regulatory standards (ISO 9001, ISO 13485, 21 CFR Part 820, or industry equivalent).
Lead and manage internal and external audits, including pre-audit preparation, execution, and CAPA follow-up.
Maintain current knowledge of applicable regulations (FDA, EU MDR, ICH, GxP) and ensure organizational compliance through proactive gap assessments.
Develop, review, and approve SOPs, work instructions, and quality documentation to ensure clarity and regulatory adherence.
Oversee change control processes, ensuring all changes are properly documented, evaluated for risk, and validated prior to implementation.

Testing, Validation & Analytical Methods

Design and execute validation protocols (IQ/OQ/PQ) for equipment, processes, software, and analytical methods.
Develop and validate test methods in compliance with relevant pharmacopeial or industry standards; perform method transfers.
Lead root cause investigation and failure analysis using structured problem-solving methodologies (8D, Ishikawa, 5-Why, FMEA).
Review and approve batch records, test results, and deviations; ensure disposition decisions are science-based and defensible.
Oversee stability programs, environmental monitoring, and in-process controls to ensure product integrity.

Cross-Functional Leadership & Continuous Improvement

Serve as the quality representative on cross-functional project teams, providing QA guidance from design through launch.
Partner with R&D, Regulatory Affairs, Manufacturing, and Supply Chain to drive quality-by-design principles.
Lead Corrective and Preventive Action (CAPA) system; track and report trends in quality metrics to senior leadership.
Mentor and coach junior QA staff, fostering a culture of quality, accountability, and continuous improvement.
Identify and implement process improvement initiatives using Lean, Six Sigma, or other quality improvement frameworks.

Qualifications

Required

Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, Engineering, or a related scientific discipline; Master's or Ph.D. preferred.
Minimum 7 years of progressive, hands-on quality assurance experience in a regulated industry (pharmaceutical, biotech, medical device, or equivalent).
In-depth knowledge of quality regulations and standards: FDA 21 CFR Parts 210/211/820, ISO 13485, ICH Q7/Q8/Q9/Q10, EU GMP Annex, or equivalent.
Proven experience designing and executing validation protocols (process, method, equipment, CSV/computer systems).
Demonstrated experience leading or supporting regulatory inspections (FDA, EMA, ISO/Notified Body) with successful outcomes.
Strong root cause analysis skills with hands-on use of tools such as FMEA, Fishbone, 5-Why, and 8D.
Experience authoring, reviewing, and approving complex quality documentation including SOPs, protocols, and technical reports.
Proficiency with quality management software (e.g., MasterControl, Veeva, TrackWise, or similar platforms).

Preferred

ASQ Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or equivalent professional certification.
Six Sigma Green Belt or Black Belt certification.
Experience with electronic batch record systems and data integrity programs (21 CFR Part 11 / Annex 11).
Prior experience with combination products or Class II/III medical devices.
Familiarity with supplier quality management and qualification programs.

Beacon Hill is an equal opportunity employer and individuals with disabilities and/or protected veterans are encouraged to apply.

California residents: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

If you would like to complete our voluntary self-identification form, please click here or copy and paste the following link into an open window in your browser: https://jobs.beaconhillstaffing.com/eeoc/

Completion of this form is voluntary and will not affect your opportunity for employment, or the terms or conditions of your employment. This form will be used for reporting purposes only and will be kept separate from all other records.

Company Profile:

Founded by industry leaders to set a new standard in search, career placement and flexible staffing, we deliver coordinated staffing solutions with unparalleled service, a commitment to project completion and success and a passion for innovation, creativity and continuous improvement.

Our niche brands offer a complete suite of staffing services to emerging growth companies and the Fortune 500 across market sectors, career specialties/disciplines and industries. Over time, office locations, specialty practice areas and service offerings will be added to address ever changing constituent needs.

Learn more about Beacon Hill and our specialty divisions, Beacon Hill Associates, Beacon Hill Financial, Beacon Hill HR, Beacon Hill Legal, Beacon Hill Life Sciences and Beacon Hill Technologies by visiting www.bhsg.com.

Benefits Information:

Beacon Hill offers a robust benefit package including, but not limited to, medical, dental, vision, and federal and state leave programs as required by applicable agency regulations to those that meet eligibility. Upon successfully being hired, details will be provided related to our benefit offerings.

We look forward to working with you!

Beacon Hill. Employing the Future™

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Refine Your Search

quality assurance engineer iii jobs in connecticut

Senior Quality Assurance Scientist

Senior Quality Engineer

Microbiology Analyst III

Magnetic Particle Inspector level 3

NDT Responsible Level III/ Department Manager

Contractor – Nuclear Quality Engineer (NQA-1) – 2008, 2009, and 2022

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