Job Market Guide: Quality Specialist jobs in Hartford-New Haven

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Quality Specialists in Hartford-New Haven. Quality Specialists in Hartford-New Haven have between ${} and ${} years of experience, averaging $${} years of experience.

40 Quality Specialist jobs in Hartford-New Haven

Devens, MA
In this role, the selected candidate will perform documentation review and support of all products frozen, stored, or shipped in the Cryogenics Facility; inspect consumables and raw materials per SOPs and material specifications.
industry
Biotech/Pharma
experience
5 - 7 years

Rensselaer, NY
Possess excellent interpersonal, written and oral communication skills with the ability to utilize active listening skills to understand concerns or reasoning in order to be responsive, gain trust and build strategic relationships.
industry
Biotech/Pharma
experience
Less than 5 years

West Greenwich, RI
To provide quality control support for cell-culture manufacturing contamination control program, and quality oversight of the environmental monitoring, utilities, and water programs. This position will work cross-functionally with site manufacturing, facility & engineering and quality, to monitor and drive continuous improvement. Further, they will work with respective global networks to represent site quality control.
industry
Biotech/Pharma
experience
5 - 7 years

Waltham, MA
In this role, the selected candidate will work on problems of diverse scope where analysis of data requires evaluation of identifiable factors; networks with senior internal and external personnel in own area of expertise.
industry
Healthcare IT
experience
5 - 7 years

Boston, MA
In this role, the selected candidate will participate and represent DFCI Imaging on multidisciplinary, inter-departmental, and/or inter-institutional process improvement projects.
industry
Education
experience
5 - 7 years

Rensselaer, NY
Responsible for supporting the work of Industrial Operations and Product Supply through the use of quality risk management (QRM).
industry
Biotech/Pharma
experience
Less than 5 years

Smithfield, RI
Manage day to day activities in the lab across Microbiology functional groups. Can lead the team and be a key decision maker in the absence of Microbiology management.
industry
Business Services
experience
5 - 7 years

New York, NY
Validate the pre-production and post-production design and functionality for ab testing.
industry
Business Services
experience
5 - 7 years

Cambridge, MA
Responsible for providing quality oversight to the change management system for change controls; this includes providing plan creation oversight, verifying that changes adhere to SOPs and regulatory compliance.
industry
Biotech/Pharma
experience
5 - 7 years

Andover, MA
Responsible for the review and approval of all documentation related to commercial manufacturing to ensure timely review and disposition of high quality batches/lots.
industry
Biotech/Pharma
experience
11 - 15 years

QA Specialist

Rensselaer, NY
Possess excellent interpersonal, written and oral communication skills with the ability to utilize active listening skills to understand concerns or reasoning in order to be responsive, gain trust and build strategic relationships.
industry
Healthcare IT
experience
Less than 5 years

West Greenwich, RI
Responsible for providing quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current good manufacturing.
industry
Biotech/Pharma
experience
5 - 7 years

Lexington, MA
In this role, you will support activities for product and material specification management, inspection support, investigation leads, operational excellence leads, document revisions, initiating/completing quality systems, provide technical support and trouble shooting, method/equipment validation and method projects activities.
industry
Software
experience
8 - 10 years

Westbury, NY
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

Billerica, MA
This position supports Marketing, Commercial, Medical Affairs, Purchasing, and Quality Assurance in the review, control, and implementation of advertising, labeling, clinical publication, and vendor control for Insulet Corporation.
industry
Business Services
experience
Less than 5 years

Rensselaer, NY
Work with management to ensure a training program exists within QA & Ops inclusive of training plans, needs analysis, training design, development and delivery, and training effectiveness evaluation.
industry
Healthcare IT
experience
Less than 5 years

QA Specialist, Product

New York, NY
Obtain a detailed understanding of the behavior of (and issues affecting) the SHOWTIME standalone streaming service and Showtime Anytime across all platforms.
industry
Business Services
experience
Less than 5 years

Rensselaer, NY
The Sr. CMC Regulatory Sciences Specialist (Product Quality Reviews) is responsible for overseeing the activities associated with the preparation, review and/or approval of product quality reviews (PQR) or other documents, as required.
industry
Biotech/Pharma
experience
5 - 7 years

Marlborough, MA
In this role, you will plans, schedules, and conducts external quality audits to assure that BSC clinical investigations comply with all applicable regulatory requirements and BSC policies and procedures.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Rensselaer, NY
The Associate Quality Systems Specialist provides oversight of Quality Management System (QMS) implementation and use. The main objective is to ensure good health of the system through the monitoring of process performance, reviewing records, reporting metrics, and leading or participating continuous improvement initiatives.
industry
Biotech/Pharma
experience
Less than 5 years

Sr QC Specialist

Lexington, MA
In addition the position will support activities for product and material specification management, inspection support, investigation leads, operational excellence leads, document revisions, initiating/completing quality systems, provide technical support and trouble shooting, method/equipment validation and method projects activities.
industry
Biotech/Pharma
experience
8 - 10 years

Mansfield, MA
Monitor and support consistent execution of MITG training process and quality training programs.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

New York, NY
Execute a wide range of quality assurance test procedures for various ad products in order to ensure that specified standards and end-user requirements have been met.
industry
New Media
experience
Not Specified

QC Sr. Specialist

Devens, MA
Perform method transfer or routine testing and data review of raw materials samples and, in-process, batch release and stability samples of Bulk Drug Substance in a cGMP compliant environment.
industry
Biotech/Pharma
experience
5 - 7 years