Job Market Guide: Quality Manager jobs in MA

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Quality Managers in MA. Quality Managers in MA have between ${} and ${} years of experience, averaging $${} years of experience.

56 Quality Manager jobs in MA

Quality Manager

Burlington, MA
Strong problem solving and analytical skills are essential for identifying and resolving problems and implementing corrective action.
industry
Manufacturing / Diversified
experience
5 - 7 years

Worcester, MA
Participates in the development of global Manufacturing Quality Assurance strategy to support pharmaceuticals, biologic, device and combination products produced.
industry
Biotech/Pharma
experience
5 - 7 years

Boston, MA
Drive increased efficiency across the teams, eliminating duplication, leveraging product and technology reuse.
industry
Manufacturing / Diversified
experience
11 - 15 years

Framingham, MA
This position is responsible for managing laboratory operations and quality systems for the QCTS department.
industry
Biotech/Pharma
experience
11 - 15 years

Boston, MA
The Sr. Manager, QA will manage the development and oversight of the QMS and support the internal and external GLP and GMP activities; establish and maintain an overall Quality System to support clinical cGMP activities.
industry
Biotech/Pharma
experience
8 - 10 years

Canton, MA
This position is responsible for performing a variety of complex tasks under general guidance and in accordance with current GMP's.
industry
Biotech/Pharma
experience
5 - 7 years

$100K - $120K - Cambridge, MA
The Manager, Process and Records Management will liaise and collaborate with clients functions to facilitate business process documentation, training compliance, records management compliance, PSMF and TMF inspection readiness state at all times.
industry
Biotech/Pharma
experience
5 - 7 years

Lawrence, MA
Driving the following company metrics to further company wide continuous improvement.
industry
Consulting
experience
Less than 5 years

Cambridge, MA
Provide quality engineering support for OPM sponsored clinical trial monitoring, including select, audit, approve new clinical trial sites, provide, or assist with, the monitoring plan, provide or assist in clinical trial site readiness audits and training for regulatory health agency inspection.
industry
Medical Devices & Diagnostics
experience
15+ years

$120K - $150K - Medford, MA
Develop and maintain product quality and reliability targets and associated specifications that can be measured and tested.
industry
Consumer Goods / Miscellaneous
experience
8 - 10 years

Boston, MA
Communicate clearly and openly with internal and external stakeholders regarding progress, roadblocks and timelines.
industry
Arts & Entertainment
experience
11 - 15 years

Billerica, MA
The Senior Manager of QA/RA Sustaining will be responsible for supporting all sustaining and continuous improvement activities for Insulet products and those of Insulet and its partners. Attention to safety, efficacy, compliance, substantial equivalence, design control, change control, manufacturing, and post market activities are all essential to this role.
industry
Business Services
experience
8 - 10 years

Boston, MA
The ideal candidate has a minimum of five years of hands-on project management experience.
industry
Business Services
experience
11 - 15 years

$120K - $170K - Boston, MA
Working with cross-functional engineering teams for NPI of product; guiding company on quality objectives.
industry
Medical Devices & Diagnostics
experience
Not Specified

$100K - $120K - Boston, MA
The Manager, Process and Records Management will liaise and collaborate with clients functions to facilitate business process documentation, training compliance, records management compliance, PSMF and TMF inspection readiness state at all times.
industry
Biotech/Pharma
experience
5 - 7 years

Boston, MA
Responsible for the collection, maintenance and dissemination of federal and state laws, regulations, accrediting agency standards for example CAP, The Joint Commission (TJC), product licenses and resource materials, and the maintenance of regulatory files. Interprets policies as needed to directors and staff.
industry
Misc. Healthcare
experience
5 - 7 years

Cambridge, MA
Direct involvement in day to day operations including FMEA facilitation, Cross Functional Change management Meetings, department streamlining/improvements, site procedure education
industry
Business Services
experience
Less than 5 years

Quality Manager

$90K - $100K - Brockton, MA
Develop and implement key performance indicators (KPIs) to support productivity and cost initiatives.
industry
Manufacturing / Electronics
experience
5 - 7 years

$50K - $140K - Lexington, MA
Responsible for supporting the development, deployment, maintenance, and improvement of the Corrective Action and Preventive Action (CAPA) Management processes and procedures within Client.
industry
Biotech/Pharma
experience
5 - 7 years

$100K - $120K - Lexington, MA
The Manager, Process and Records Management will liaise and collaborate with clients functions to facilitate business process documentation, training compliance, records management compliance, PSMF and TMF inspection readiness state at all times.
industry
Biotech/Pharma
experience
5 - 7 years

$120K -$160K - Cambridge, MA
Develop test methods and inspection procedures and implement process control systems to support the development, qualification, and on-going manufacturing of products
industry
Medical Devices & Diagnostics
experience
Not Specified

Cambridge, MA
In this role, you will facilitate compliance reviews and audit of select documentation for investigation drugs and for product marketing applications respectively.
industry
Biotech/Pharma
experience
5 - 7 years

QA Manager

Agawam, MA
Supports the Quality Lead for Deviations/CAPA as a Subject Matter Expert (SME) for the Baxalta Global Event Management Systems (GEMS, Current and Legacy systems).
industry
Retail / Health & Pharmacy
experience
8 - 10 years

MA
Review and approve batch records for all labeling and packaging operations; ensure proper version control and document integrity of packaging component labeling, specifications, printed labeling artworks and other assigned labeling documents.
industry
Healthcare IT
experience
11 - 15 years