Job Market Guide: Quality Specialist jobs in Providence-New Bedford

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

27 Quality Specialist jobs in Providence-New Bedford

Waltham, MA
In this role, you will perform evaluation of internal controls, communications, risk assessments, and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards.
industry
Healthcare IT
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

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

Worcester, MA
Lead, or provide expertise within, the Data Integrity Risk Management Process for Laboratory and/or Manufacturing Systems.
industry
Biotech/Pharma
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

Lexington, MA
Work on moderate to complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.
industry
Software
experience
Less than 5 years

Manchester, NH
Works on a variety of moderate to complex projects to ensure organizational compliance, efficiency and effectiveness. Performs research, data collection, analysis and report preparation.
industry
Patient Care
experience
Less than 5 years

Lexington, MA
Work on moderate to complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.
industry
Software
experience
5 - 7 years

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

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

Lexington, MA
This position is responsible for monitoring compliance to the Shire QMS, and other established IT Corporate procedures.
industry
Software
experience
8 - 10 years

Westford, MA
Direct activities within their supply and commodity base. Oversee corrective and preventive action.
industry
Aerospace / Defense
experience
5 - 7 years

QC Specialist II

Lexington, MA
Data analysis, data trending, project and testing coordination, support of product specification management, COA generation, material specification creation, document revisions.
industry
Software
experience
Less than 5 years

Quality Specialist

Boston, MA
Developing and executing manual and automated tests to ensure functional and non-functional requirements (performance, resilience, scalability, usability, security, and corporate compliance) are satisfied.
industry
Business Services
experience
Not Specified

Lexington, MA
This is a senior individual contributor role with primary responsibility for supporting engineering and validation programs and projects, facility projects, technology transfer, and supporting any cross-site Facilities/Engineering/Validation initiatives.
industry
Software
experience
5 - 7 years

Lexington, MA
Managing QA oversight through the provision of compliance and technical input into all project phases i.e. from design through to the commissioning and qualification execution phases of the project.
industry
Software
experience
5 - 7 years

Lowell, MA
The Quality Improvement Specialist-Nursing under the supervision of the Quality Manager performs services in Regulatory Compliance according to the policies, procedures, philosophy, and objectives of the department and hospital.
industry
Patient Care
experience
Less than 5 years

Boston, MA
Experienced in implementing Agile scrum methodology developing and leading software QA programs and teams developing test metrics, test strategy, test plans, built test beds and automation infrastructure built frameworks to execute tests and analyzing results.
industry
Consulting
experience
Not Specified

QA Specialist

Lexington, MA
Responsible for establishment and continuous improvement of distribution and supply chain quality processes, driving for compliance and efficiency while allowing local flexibility.
industry
Software
experience
5 - 7 years

Lexington, MA
Develop and aid in development of solutions for minor to moderately complex problems.
industry
Software
experience
Less than 5 years

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

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

Smithfield, RI
Support of regulatory submissions and agency queries; maintain knowledge of current industry practices relative to Microbiology activities.
industry
Patient Care
experience
5 - 7 years

Boston, MA
This position is responsible for handling product complaints to ensure compliance with US and International regulatory agencies.
industry
Biotech/Pharma
experience
Less than 5 years