Job Market Guide: Quality Assurance Manager jobs in Springfield-Holyoke

Competition
High
0.758003
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Quality Assurance Managers in Springfield-Holyoke. Quality Assurance Managers in Springfield-Holyoke have between ${} and ${} years of experience, averaging $${} years of experience.

48 Quality Assurance Manager jobs in Springfield-Holyoke

Boston, MA
Establish and maintain company compliance to ISO-9001 and ISO-13485 and ensure inspection standards to meet IPC and J-Standard required by customers.
industry
Consumer Electronics
experience
8 - 10 years

Cambridge, MA
Provide QA support to ensure data is generated, documented (recorded), and reported in compliance with Good Clinical Practice and the applicable requirements
industry
Biotech/Pharma
experience
8 - 10 years

Cambridge, MA
Manage the implementation, qualification, validation and transfer of analytical methods.
industry
Misc. Healthcare
experience
8 - 10 years

Haverhill, MA
Responsible for ensuring that defined processes and outputs deliver the high quality chemical solutions for the electronics industry with specific focus on the semiconductor segment from incoming QC, in-process QC and outgoing QC for the final products.
industry
Life Sciences & Research
experience
8 - 10 years

Boston, MA
The Quality Assurance Manager works with numerous development and business teams to help ensure the correct business functionality, client and technology requirements, and industry standards are tested within the envisioned solution.
industry
Financial Services
experience
8 - 10 years

Cambridge, MA
Act as Research and Development Pharmacovigilance Quality Assurance function in the respective region. Ensure that system audits are conducted, communicating any critical compliance risks noted from these activities to senior management, and ensuring that corrective actions are implemented.
industry
Biotech/Pharma
experience
8 - 10 years

$100K - $130K - Newburyport, MA
The Senior Quality Assurance Manager will plan, direct and coordinate the development, application, and maintenance of all quality systems for inspecting incoming product, raw material, in-process material and products thru to a finished product in conformance with ISO 13485 standards.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Cambridge, MA
Act as Research and Development Pharmacovigilance Quality Assurance function in the respective region. Ensure that system audits are conducted, communicating any critical compliance risks noted from these activities to senior management, and ensuring that corrective actions are implemented.
industry
Biotech/Pharma
experience
8 - 10 years

East Greenwich, RI
lead efforts to develop, document, and implement applicable QA processes and procedures to provide more effective quality methods within the group in support of providing quality products.
industry
Apparel & Footwear
experience
5 - 7 years

Lowell, MA
Leading the global team on quality assessment of the workforce ready release, primary stakeholder in making go/no-go decision.
industry
Business Services
experience
11 - 15 years

Beverly, MA
Manage, review and update documentation for quality control protocols.
industry
Biotech/Pharma
experience
5 - 7 years

Boston, MA
Ensures Departmental files including Media Lab are current and documentation is complete and in compliance with all requirements.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Manager of QA

Boston, MA
Demonstrate passion for the continuous improvement of processes and methodologies used in the development of software solutions.
industry
Business Services
experience
5 - 7 years

Bridgeport, CT
In this role, the selected candidate will oversee the maintenance of clinical records and files to comply with Conditions of Participation (COPs), using measurements, as licensure, certification, and accreditation results.
industry
Misc. Healthcare
experience
Less than 5 years

Waltham, MA
Review and Document Control support. Responsible for Labeling reviews, Complaint trending and other metrics with reporting May have some customer interaction.
industry
Biotech/Pharma
experience
5 - 7 years

$105K - $135K - Wellesley, MA
As the Quality Assurance Manager, you will be responsible for a site wide transition from TS 16949 to IAFT 16949. The position will report directly to the Corporate Director of Quality. Other roles and responsibilities of the role include:
industry
Automotive
experience
Less than 5 years

Manchester, NH
Work closely with Manufacturing Engineer to assure clear work instructions are available and understood throughout the production departments.
industry
Telecommunications
experience
5 - 7 years

Boston, MA
Conducting and coordinating quality reviews over audit work papers, audit methodologies and other division processes.
industry
Business Services
experience
5 - 7 years

Cambridge, MA
Monitor compliance issues identified across clinical programs. Analyze audit program results, quality issues, and quality investigations in order to optimize global operations and overall global state of compliance.
industry
Biotech/Pharma
experience
5 - 7 years

Haverhill, MA
Responsible for ensuring that defined processes and outputs deliver the high quality chemical solutions for the electronics industry with specific focus on the semiconductor segment from incoming QC, in-process QC and outgoing QC for the final products. Conduct analytical equipment qualification and laboratory relevant computerized system validation support validation of cleaning procedures.
industry
Business Services
experience
8 - 10 years

Rensselaer, NY
The Manager, Quality Assurance, is responsible for providing professional expertise and leadership in the Quality function. The Manager is responsible, along with the Head of Quality Assurance, for ensuring that all manufactured materials are in accordance with the Companys quality assurance program and quality/reliability standards to satisfy cGMP regulatory requirements and customer specifications and expectations.
industry
Information Services
experience
5 - 7 years

Beverly, MA
Review and Document Control support. Responsible for Labeling reviews, Complaint trending and other metrics with reporting May have some customer interaction.
industry
Biotech/Pharma
experience
5 - 7 years

Cambridge, MA
Evaluate, develop, implement, and manage processes to support the VBD (Vaccine Business Division) GMP Quality Control (QC) organization. This role partners with global colleagues to provide leadership and ensure there is a compliant, efficient and scalable processes throughout the VBD organization.
industry
Biotech/Pharma
experience
11 - 15 years