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

Competition
High
0.809029
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.

62 Director of Quality jobs in Hartford-New Haven

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

Boston, MA
Assess compliance with BSA/sanctions related regulations and established Bank policies and procedures and identify any potential and emerging BSA/sanctions/fraud risks or issues.
industry
Financial Services
experience
5 - 7 years

Andover, MA
Ownership of companys quality processes and development of strategic quality, vision, mission, goals, and objectives in conjunction with the companys strategic plan.
industry
Engineering Services
experience
11 - 15 years

New York City, NY
Maintain up-to-date standards of proficiency in the areas of accounting and auditing while keeping the Firm in compliance with quality control elements.
industry
Financial Services
experience
11 - 15 years

Tewksbury, MA
This role will develop, maintain and revise policies and procedures for pharmacy operations to prevent illegal, unethical or improper conduct.
industry
Patient Care
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

Burlington, MA
Establish and maintain a risk-based and scientific-based quality system to protect the public health and to meet AMRI' s business needs.
industry
Information Services
experience
11 - 15 years

Melville, NY
Ensures all work is performed in a safe, effective manner, and in compliance with the appropriate industry and regulatory standards, and Departmental, Plant, and Corporate quality and Behavioral Based Safety ( BBS ) goals.
industry
Business Services
experience
11 - 15 years

Lexington, MA
Ensuring that Shire has a cGMP compliant and cost efficient QRM System fully integrated into global and site business processes and continuously improved through Quality subject matter expertise.
industry
Biotech/Pharma
experience
11 - 15 years

Waltham, MA
Ability to deal with ambiguity and the corresponding capacity to make decisions or recommendations based on potentially incomplete information.
industry
Information Services
experience
11 - 15 years

$130K - $200K - Framingham, MA
Establish, develop and manage the companys quality management system (QMS) in compliance with US regulations and standards for Combination Products (Medical Devices and Biologics/Cell Therapy).
industry
Biotech/Pharma
experience
11 - 15 years

$130K - $200K - Boston, MA
Establish, develop and manage the companys quality management system (QMS) in compliance with US regulations and standards for Combination Products (Medical Devices and Biologics/Cell Therapy).
industry
Biotech/Pharma
experience
11 - 15 years

Melville, NY
Ensure compliance with all DEA controlled substance requirements Manages, tracks, and trends customer complaints Tracks and trend all site commitments Leads Quality Risk Management and Compliance Excellence programs Facilitates Site Quality Council.
industry
Business Services
experience
11 - 15 years

$130K - $200K - Holliston, MA
Establish, develop and manage the companys quality management system (QMS) in compliance with US regulations and standards for Combination Products (Medical Devices and Biologics/Cell Therapy).
industry
Biotech/Pharma
experience
11 - 15 years

$130K - $200K - Franklin, MA
Establish, develop and manage the companys quality management system (QMS) in compliance with US regulations and standards for Combination Products (Medical Devices and Biologics/Cell Therapy).
industry
Biotech/Pharma
experience
11 - 15 years

Queens, NY
Facilitate the preparation of Annual Action Plans, in support of long range strategic plans, for submission at the beginning and end of the year.
industry
Business Services
experience
Less than 5 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

Lowell, MA
Lead failure investigation and corrective action for customer related failures, and facilitate customer quality & reliability interactions.
industry
Electronics
experience
11 - 15 years

Boston, MA
Create teams and infrastructure to support automated and manual testing of the many Chewy software applications.
industry
Arts & Entertainment
experience
Not Specified

Waltham, MA
Able to lead and develop team QA professionals that will be direct reports as well as to leverage external resources to achieve robust quality oversight.
industry
Biotech/Pharma
experience
15+ years

Waltham, MA
Able to lead and develop team QA professionals that will be direct reports as well as to leverage external resources to achieve robust quality oversight.
industry
Biotech/Pharma
experience
11 - 15 years

Billerica, MA
Advanced working knowledge of QA processes and methodologies; expertise in test planning, test case management, code coverage and defect analysis.
industry
Software
experience
11 - 15 years

Waltham, MA
Drives achievement of Quality objectives through leadership of direct reports, while providing Quality oversight to GCP, GLP and GVP regulated processes throughout the business.
industry
Biotech/Pharma
experience
15+ years

Westwood, MA
Director of Quality and Education plans, directs, coordinates and evaluates operations of the quality and education departments.
industry
Misc. Healthcare
experience
11 - 15 years