Job Market Guide: Director of Quality jobs in New York

Competition
Avg
0.65485
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Director of Qualitys in New York. Director of Qualitys in New York have between ${} and ${} years of experience, averaging $${} years of experience.

70 Director of Quality jobs in New York

Philadelphia, PA
This person will also have in-depth knowledge of helpdesk operations and ITIL functions centered on Incident, Problem, Change and Service Level Management.
industry
Manufacturing / Diversified
experience
8 - 10 years

$150K - $190K - Livingston, NJ
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
8 - 10 years

$168K - $204K - Caldwell, NJ
In this role, the selected candidate will be responsible for managing the R&D Quality Assurance activities including all R&D related audits and associated quality system processes within the GCP, GLP and cGMP.
industry
Biotech/Pharma
experience
8 - 10 years

$105K - $130K - Bedminster, NJ
This person will be responsible for ensuring CMC QA document review and approvals are performed in a manner that supports clinical release, regulatory approval, and commercialization of the companys drug product programs.
industry
Staffing & Recruiting
experience
Not Specified

East Greenville, PA
Implement programs to establish and/or monitor stability and capability of Knoll manufacturing operations, with respect to production of Knoll product designs to required specifications.
industry
Business Services
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

RADNOR, PA
This position is responsible for technical ownership of a proprietary specialized chemical purification and production process, within a leading international chemical supplier to laboratories, biotechnology and pharmaceutical companies.
industry
Business Services
experience
8 - 10 years

QA Associate Director

New York, NY
Manage and plan work activities for a team of both employees and onshore and offshore contractors who are responsible for delivering various testing activities.
industry
Healthcare IT
experience
11 - 15 years

New York, 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
Business Services
experience
11 - 15 years

QA Associate Director

$160K - $180K - New York, NY
Manage and plan work activities for a team of both employees and onshore and offshore contractors who are responsible for delivering various testing activities.
industry
Healthcare IT
experience
11 - 15 years

West Point, PA
Responsible for driving MPS throughout the organization to enable change in the operating systems, management systems, and mindsets, behaviors and capabilities of our people to produce product at the highest quality, for the lowest cost, and in the shortest lead time.
industry
Biotech/Pharma
experience
11 - 15 years

$110K - $140K - Brooklyn, NY
In this role, the selected candidate will be responsible for providing education and consultation to internal and external constituents regarding quality and outcomes management activities.
industry
Staffing & Recruiting
experience
5 - 7 years

Exton, PA
Support Corporate and Supplier quality audit programs. Ensure that the audit programs are maintained as required by internal policies and procedures.
industry
Information Services
experience
11 - 15 years

Whitehouse Station, NJ
Responsible for driving MPS throughout the organization to enable change in the operating systems, management systems, and mindsets, behaviors and capabilities of our people to produce product at the highest quality, for the lowest cost, and in the shortest lead time.
industry
Biotech/Pharma
experience
11 - 15 years

$105K - $130K - Bedminster, NJ
This person will be responsible for ensuring CMC QA document review and approvals are performed in a manner that supports clinical release, regulatory approval, and commercialization of the companys drug product programs.
industry
Biotech/Pharma
experience
Not Specified

$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

Philadelphia, PA
Review workpapers and financial statements for compliance with professional and firm standards; 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
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

New York, NY
Searching for a Director - Quality Control.
industry
Consulting
experience
Not Specified

Philadelphia, PA
The Associate Director, Quality Systems will ensure quality and regulatory compliance requirements are identified, documented, integrated, and maintained.
industry
Medical Devices & Diagnostics
experience
8 - 10 years

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

Toms River, NJ
Responsible for the planning, implementation and monitoring of Quality, Performance Improvement, and Safety activities for a designated group of clinical, ancillary, administrative and support areas of CMC's health care system.
industry
Healthcare IT
experience
Not Specified

New Brunswick, NJ
Implement effective Quality Product Complaints processes including investigation procedures, documentation systems, tools, metrics and measurable improvements.
industry
Biotech/Pharma
experience
11 - 15 years