Job Market Guide: Quality Assurance Specialist jobs in New York

Competition
Avg
0.378028
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Quality Assurance Specialists in New York. Quality Assurance Specialists in New York have between ${} and ${} years of experience, averaging $${} years of experience.

30 Quality Assurance Specialist jobs in New York

Center Valley, PA
The Environmental Monitoring/Metrology Specialist will be responsible for multiple aspects to support current Good Manufacturing Practice (cGMP) systems during manufacture of clinical material.
industry
Biotech/Pharma
experience
Less than 5 years

Piscataway, NJ
In this role you will be responsible for project evaluation and market research while showcasing an understanding of the Customer and Employee experiences.
industry
Business Services
experience
Not Specified

$45K - New York, NY
As the Quality Assurance Specialist you will lead initiative to track, oversee and manage the employer confirmation process by working closely with the Senior Account Manager as well as the Sales and Recruitment teams to ensure timely submission of employer confirmations and compliance with the New York City Department of Small Business Services policies.
industry
Education
experience
Less than 5 years

Lehigh Valley, PA
The Environmental Monitoring/Metrology Specialist will be responsible for multiple aspects to support current Good Manufacturing Practice (cGMP) systems during manufacture of clinical material.
industry
Biotech/Pharma
experience
Less than 5 years

$85K - NJ
The Quality Assurance Validation Specialist is an adept technical writer/editor and the use of desktop Office applications. The QA Validation Specialist must become familiar with site databases and proficient in the retrieval and presentation of information.
industry
Biotech/Pharma
experience
5 - 7 years

West Point, PA
In this role, you will support the development of action plans to resolve atypical events and serves as a role model to others within the organization to ensure compliance with cGMPs and regulatory requirements to support the quality, safety, efficacy, and potency of Merck products.
industry
Biotech/Pharma
experience
Less than 5 years

Pleasantville, NJ
In this role, you will be using back end analytics to increase efficiency of installation practices within the assigned markets.
industry
Business Services
experience
Less than 5 years

$85K - NJ
The Quality Assurance Validation Specialist is an adept technical writer/editor and the use of desktop Office applications.
industry
Staffing & Recruiting
experience
Not Specified

Moonachie, NJ
In this role, you will Work closely with plant to assure continued improvement of quality through communication and review of product compliance to specification.
industry
Consumer Goods / Miscellaneous
experience
5 - 7 years

West Point, PA
In this role, you will demonstrated interpersonal skills including flexibility, collaboration and inclusion skills, and ability to work in a team environment.
industry
Biotech/Pharma
experience
Not Specified

$55K - $66K - West Nyack, NY
In this role, you will develop standards of performance in accordance with The companys three phase process review.
industry
Business Services
experience
Less than 5 years

Horsham, PA
In this role, the selected candidate will participate in user acceptance testing (UAT) of new software and the subsequent software releases by providing feedback to IT on user experience, representing a non-technical user audience.
industry
Biotech/Pharma
experience
Less than 5 years

Allentown, PA
The Environmental Monitoring/Metrology Specialist will be responsible for multiple aspects to support current Good Manufacturing Practice (cGMP) systems during manufacture of clinical material.
industry
Biotech/Pharma
experience
Less than 5 years

Cherry Hill, NJ
In this role, you will provide regulatory compliance support by supporting product vision process adherence and label review.
industry
IT Consulting/Services
experience
Less than 5 years

Exton, PA
The Sr. Quality Systems Quality Assurance Associate is responsible for assisting with the day to day operations related to the Quality Standards program and data analytics within the Quality Systems department.
industry
Biotech/Pharma
experience
5 - 7 years

West Point, PA
In this role, you will be responsible for ensuring that all products managed by EQA are manufactured, packaged, analyzed, released stored, and distributed in accordance with Merck/MSD expectations and all applicable regulatory requirements.
industry
Biotech/Pharma
experience
5 - 7 years

West Point, PA
The incumbent exercises a role in monitoring and maintaining the external manufacturers/partners compliance with the FDC Act, Current Good Manufacturing Practices Regulations (domestic and foreign) and other pertinent legal requirements in accordance with Quality and Supply Agreement terms and Company Policy.
industry
Biotech/Pharma
experience
Less than 5 years

Bethlehem, PA
The Environmental Monitoring/Metrology Specialist will be responsible for multiple aspects to support current Good Manufacturing Practice (cGMP) systems during manufacture of clinical material.
industry
Biotech/Pharma
experience
Less than 5 years

Quakertown, PA
The Sr. Quality Systems Specialist to support our growing demand. The Quality Systems Specialist is tasked with ensuring product performance and consumer safety.
industry
Healthcare IT
experience
5 - 7 years

QA / QC Specialist

Hauppauge, NY
In this role, the selected candidate will ensure design meets all local, state and federal regulatory compliance; ensure compliance with all internal Quality Control processes.
industry
Engineering Services
experience
15+ years

New Haven, CT
This person is responsible for reviewing imaging data (i.e. MRI, PET, SPECT) to confirm specific protocol requirements have been met as well as ensuring technical adequacy and data integrity.
industry
Business Services
experience
5 - 7 years

$80K - $90K - NJ
In this role, you will be responsible for Validation Specialist will provide project support for the New Product launches and utilize Microsoft Project to organize site deliverables.
industry
Biotech/Pharma
experience
5 - 7 years

$80K - $90K - Somerset, NJ
Must be able to check and solve issues which effect the product validation or the regulatory state; involve in providing project support for the New Product and cross functional with multi departments.
industry
Medical Equipment
experience
5 - 7 years

Moorestown, NJ
In this position, you will execute an annual QA plan by specialty practice including identification and testing of standards based on key risk areas.
industry
Misc. Healthcare
experience
5 - 7 years

Morristown, NJ
The Sr. Quality Systems Specialist to support our growing demand. The Quality Systems Specialist is tasked with ensuring product performance and consumer safety.
industry
Healthcare IT
experience
5 - 7 years