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

Competition
Avg
0.466988
Based on job seekers per open jobs
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.

24 Quality Specialist jobs in Providence-New Bedford

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

Salem, NH
The Quality Assurance Specialist supports the QA Lead and the companys quality program by auditing chemists analytical data, routine work, protocols and reports.
industry
Biotech/Pharma
experience
Less than 5 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

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

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

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

West Greenwich, RI
Quality specialist will lead the development and execution of validation strategies, ensure validation activities are performed in a consistent and controlled manner.
industry
Biotech/Pharma
experience
Less than 5 years

Bloomfield, CT
In this role, you will collaborate with source systems and downstream data consumers to remediate issues and put in place processes to monitor data quality risks.
industry
Manufacturing / Diversified
experience
8 - 10 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

QA IT Specialist

Lexington, MA
In this role, you will identify and manage continuous improvement projects that may span multiple functions or departments with the objective of achieving quality, reliability and cost improvements.
industry
Biotech/Pharma
experience
8 - 10 years

Boston, MA
In this role, the successful candidate will perform BSA/AML, sanctions, FCPA, and fraud related testing at the Enterprise level, business or support units, and bank subsidiaries.
industry
Financial 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

Smithfield, RI
In this role, the selected candidate must have a good working knowledge of electronic systems including Trackwise, LIMS, as well as electronic documentation management systems.
industry
Business Services
experience
5 - 7 years

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

Marlborough, MA
In this role, the selected candidate will be responsible for facilitating various quality system related meetings, and identifying continuous improvement opportunities impacting the capa and nce process.
industry
Business Services
experience
5 - 7 years

Quality Specialist

Andover, MA
In this role, you will have working knowledge of appropriate global medical device regulations, requirements, and standard.
industry
Energy & Environmental Services
experience
5 - 7 years

Marlborough, MA
In this role, you will participate on clinical project teams and influence and encourage clinical teams towards a state of inspection readiness at all times.
industry
Medical Devices & Diagnostics
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

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

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

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

QA Specialist

Lexington, MA
In this role, you will be responsible for inspection readiness, for hosting inspections, and for responses to inspections by, health authorities and partner and third party audits.
industry
Biotech/Pharma
experience
5 - 7 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

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