Job Market Guide: Director of Quality jobs in Hartford-New Haven

Competition
High
0.851879
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Director of Qualitys in Hartford-New Haven. Director of Qualitys in Hartford-New Haven have between ${} and ${} years of experience, averaging $${} years of experience.

66 Director of Quality jobs in Hartford-New Haven

$132K - $165K - Taunton, MA
Support engineering as it develops product designs and production production processes through use of quality engineering tools (FMEA, risk mitigation, verification and validation practices.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Clifton, NJ
Establish and maintain a quality assurance program ensuring compliance with medical, military and GMP specifications; direct inspection activities, test procedures, and utilization of test equipment.
industry
Manufacturing / Plastics
experience
8 - 10 years

$132K - $165K - Canton, MA
Support engineering as it develops product designs and production production processes through use of quality engineering tools (FMEA, risk mitigation, verification and validation practices.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Dir II - Quality

Merrimack, NH
Interface with customers on quality requirements and performance.2. Provide direction, supervision, and guidance to ensure alignment with policy, strategic objectives and organizational goals.
industry
Manufacturing / Diversified
experience
15+ years

Secaucus, NJ
The Director of Quality position is responsible for driving Lean/Six Sigma strategic improvements and innovative change throughout the organization.
industry
Security
experience
Not Specified

Lexington, MA
Oversight of corporate quality compliance functions including but not limited to management of complaints, audits, CAPAs, non-conformances, deviations, change management, and document management.
industry
Medical Devices & Diagnostics
experience
15+ years

Cambridge, MA
Partner with cross-functional peers to drive and enable product reliability design improvements via ongoing research, design and further development of existing products to continuously improve device reliability, quality, and customer satisfaction.
industry
Biotech/Pharma
experience
8 - 10 years

Boston, MA
Create accountability for analytic projects; ensure resources dont get stuck in doing ongoing analysis where we can more rapidly move to business-impacting decisions.
industry
Furniture & Home Goods
experience
8 - 10 years

Boston, MA
Translate the Pharma customer Quality requirements above the ISS Group Quality Manual into project plans and compliance programs.
industry
Biotech/Pharma
experience
5 - 7 years

$132K - $165K - Braintree, MA
Support engineering as it develops product designs and production production processes through use of quality engineering tools (FMEA, risk mitigation, verification and validation practices.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Bellows Falls, VT
Manage the Quality Assurance and Quality Control (Testing and Measurement) Departments; provide coaching, counseling, advice, support and motivation to the team to help them achieve quality objectives.
industry
IT Consulting/Services
experience
5 - 7 years

Hartford, CT
Reporting to top management on the effectiveness of the Quality Management System. Recommending and implement system improvements. Ensuring the Quality Management System meets the requirements of ISO 9001 and other requirements as required by contract. Managing the processes for internal and external audit and corrective and preventive action.
industry
Manufacturing / Diversified
experience
11 - 15 years

Melville, NY
Conduct regular Management Reviews, manage complaints, non-conformances and CAPAs.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Boston, MA
Manage and direct at all levels of testing- this includes unit, automation, regression, functional, performance and scalability testing.
industry
Consulting
experience
11 - 15 years

Amityville, NY
Ensures thorough investigations are performed leading to the assignment of root causes and the implementation of effective corrective/preventive actions (CAPA) to minimize the possibility of recurrence.
industry
Manufacturing / Packaging
experience
8 - 10 years

Wilmington, MA
Works with subject matter experts to ensure appropriate and comprehensive training plans are created and executed including the design of curriculums and development of content.
industry
Data Storage
experience
5 - 7 years

Andover, MA
Provide leadership for the Supplier Quality function across Diagnostic Imaging and establish a common approach and working methods to drive one Philips towards Supply Base.
industry
Energy & Environmental Services
experience
8 - 10 years

Cambridge, MA
The Director of Device Quality Engineering will lead and build a dynamic team that supports new product development across the organization.
industry
Biotech/Pharma
experience
8 - 10 years

$100K - $200K - Stratford, CT
Determine criterion for supplier quality, qualify them, and assure the quality of incoming parts.
industry
Food & Beverage
experience
8 - 10 years

Andover, MA
The QA Director will own end-to-end product and solution quality, including designing test frameworks, and tools for testing in QA and production environments, gathering a variety of data to support sophisticated quality metrics, and other quality related programs.
industry
Telecommunications
experience
5 - 7 years

Lexington, MA
Deploying the QRM Training Program and developing and training personnel and internal customers on QRM business processes.
industry
Software
experience
11 - 15 years

Merrimack, NH
The Sr. Director designs and builds a comprehensive data program as a key leader in the business and partnering with IT on mapping the architecture, creates practices for data governance, ensures accessibility, creates standardization and ownership.
industry
Software
experience
11 - 15 years

Clinton, MA
Responsible for Management Responsibilities (Management Review, Quality Objectives, Quality policy), Quality Engineering, Design Quality Assurance, Quality Systems, Supplier Quality, Complaint Management, Incoming and Finiahed product Quality, Document Control, Non-conforming Materials (MRB).
industry
Semiconductors
experience
8 - 10 years

Rensselaer, NY
Perform compliance monitoring of area operations, including trending of NOEs/EOEs, and DNFs and evaluating effectiveness of corrective actions.
industry
Biotech/Pharma
experience
11 - 15 years

Cambridge, MA
Manage the data integrity (QC) program to ensure data in regulatory filings has been verified against source data for accuracy.
industry
Business Services
experience
15+ years