1

Quality Management System Manager Jobs in Connecticut

Manager, Quality

Wallingford, CT · On-site

$91K - $150K/yr

Lead quality management system review and improvement process. * Approval of all new and updated process validations. * Collaborate with development and facilitate new product/process design and ...

Manager, Quality

Wallingford, CT · On-site

$91K - $150K/yr

Lead quality management system review and improvement process. * Approval of all new and updated process validations. * Collaborate with development and facilitate new product/process design and ...

Manager, Quality

Wallingford, CT · On-site

$92 - $151/hr

Lead quality management system review and improvement process. * Approval of all new and updated process validations. * Collaborate with development and facilitate new product/process design and ...

New

Understand elements of a Quality Management System and its development, documentation and implementation to applicable domestic and international standards and/or requirements * Understand the audit ...

Quality Manager

Wallingford, CT · On-site

$90 - $130/hr

... Management System, setting up and maintaining controls and documentation. * Partnering with site management in managing site quality operations and recommending relevant Q KPIs for follow-up of the ...

Ensure alignment of CAPA processes with global regulatory requirements21 CFR Part 820, 21 CFR Parts 210/211, ISO 13485, the FDA Quality Management System Regulation (QMSR), and the EU Medical ...

Quality Manager, Operations

Danbury, CT · On-site

$110K - $125K/yr

Summary The Manager of Quality is responsible for supporting Belimo's Integrated ... Management System, as well as overseeing functions such as Incoming Material Inspection, Warranty ...

Quality Manager, Operations

Danbury, CT · On-site

$110K - $125K/yr

Summary The Manager of Quality is responsible for supporting Belimo's Integrated ... Management System, as well as overseeing functions such as Incoming Material Inspection, Warranty ...

Quality Engineer

Torrington, CT · On-site

$70K - $90K/yr

This position is responsible for the implementing the Quality Management System under the direction of the Quality Assurance Manager to assure that all products manufactured by the organization meet ...

Quality Engineer

Torrington, CT · On-site

$70K - $90K/yr

This position is responsible for the implementing the Quality Management System under the direction of the Quality Assurance Manager to assure that all products manufactured by the organization meet ...

Quality Manager

Wallingford, CT · On-site

$90K - $120K/yr

... Management System, setting up and maintaining controls and documentation. * Partnering with site management in managing site quality operations and recommending relevant Q KPIs for follow-up of the ...

Showing results 21-40

Quality Management System Manager information

What is the difference between Quality Management System Manager vs Quality Assurance Manager?

AspectQuality Management System ManagerQuality Assurance Manager
Primary FocusDeveloping, implementing, and maintaining quality management systemsOverseeing quality assurance processes and testing
CertificationsISO 9001 Lead Auditor, CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentQuality departments, compliance teamsProduction, manufacturing, or service delivery areas
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

The Quality Management System Manager focuses on establishing and maintaining comprehensive quality systems, ensuring compliance with standards like ISO 9001. In contrast, the Quality Assurance Manager concentrates on testing, inspections, and ensuring products or services meet quality requirements. Both roles are essential for quality improvement but differ in scope and daily responsibilities.

What does a quality management system manager do?

A quality management system manager oversees the development, implementation, and maintenance of quality management systems to ensure products and services meet company standards and regulatory requirements. They analyze processes, conduct audits, and coordinate continuous improvement initiatives, often using tools like ISO standards and quality metrics. Strong leadership, communication skills, and knowledge of quality tools are essential for this role.

What is the role of a quality management system manager?

A quality management system manager oversees the development, implementation, and maintenance of quality management systems to ensure products and services meet industry standards and customer requirements. They analyze processes, conduct audits, and coordinate with teams to improve quality, often utilizing standards like ISO 9001. Strong organizational, analytical, and communication skills are essential for this role.

What are the most commonly searched types of Quality Management System jobs in Connecticut?

The most popular types of Quality Management System jobs in Connecticut are:

What cities in Connecticut are hiring for Quality Management System Manager jobs?

Cities in Connecticut with the most Quality Management System Manager job openings:

Infographic showing various Quality Management System Manager job openings in Connecticut as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 13% Part Time, 2% Temporary, and 4% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Manager, Quality

Bio-Techne

Wallingford, CT • On-site

$91K - $150K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago


Bio-Techne rating

8.4

Company rating: 8.4 out of 10

Based on 15 frontline employees who took The Breakroom Quiz


Job description

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.

Pay Range:

$91,700.00 - $150,800.00

Position Summary:

Position will manage the Quality Management System activities of Bio-Techne's Wallingford site, including but not limited to document control, training, validations, CAPA, NCMRs and deviations among others. This position will lead the qualification process related to the new processes and process improvements may also assist with the software validation process.

Key Responsibilities:

  • Manage personnel in the department providing guidance, tools and conducting performance discussions

  • Write, review & approve the following as appropriate: SOP, COA, Deviation, & Change Impact Assessment

  • Lead process to ensure compliance with Wallingford Quality Management System.

  • Leads process to solve product and process related issues and non-conformances and optimization

  • Lead process to identify and implement process improvement and optimization.

  • Lead quality management system review and improvement process.

  • Approval of all new and updated process validations.

  • Collaborate with development and facilitate new product/process design and validation

  • Follow guidelines and comply with all company safety, quality, and training procedures and regulations

  • Perform additional duties as assigned

QUALIFICATIONS

Education and Experience:

  • Bachelor's degree and 8 or more years of relevant experience

  • Or, Master's degree in a related field and 2-5 years of relevant experience

  • Demonstrated leadership capacity with 3-5 years of formal or informal leadership experience.

Knowledge, Skills, and Abilities:

  • Ability to lead a team of various skills levels and background.

  • Working knowledge of Microsoft Word and Excel is required

  • Must be able to work in a fast-faced environment where you will be required to prioritize your own work and the work of others to meet various project deadlines

  • Must be able to analyze data to make effective decisions

  • Must have good verbal and written communication skills, especially across different groups

  • Must have strong organizational skills and attention to detail

  • Must work well independently in an environment that requires strategic decision making

  • Proficient in planning, organizational, and multi-tasking skills to complete assignments in an efficient manner in a fast-paced environment.

  • Must be able to effectively train new employees

  • Must be able to effectively lead new projects, especially across different groups

  • Must stay informed of current trends and developments in area of expertise

Working Conditions:

  • Work performed in a laboratory and production environment with exposure to chemicals, reagents, and standard lab equipment.

  • Standard schedule hours with occasional variation depending on production needs.

  • Onsite work required during standard business hours.

Physical Requirements:

  • Ability to stand, walk, and perform repetitive laboratory tasks for extended periods.

  • Manual dexterity required for laboratory equipment and fine measurement techniques.

  • Ability to work at a computer for extended periods.

  • Ability to lift and handle materials weighing 5-20 lbs.


Why Join Bio-Techne:

  • We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
  • We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
  • We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
  • We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.
  • We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
  • We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

Bio-Techne is an E-Verify Employer in the United States.


All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.


To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.


This position requires work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States (e.g., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant work status). If you require a reasonable accommodation to complete an application, participate in an interview, or take part in any other stage of the recruitment process, please contact hr@bio-techne.com for assistance.


What Bio-Techne employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom