Quality/Process Auditor - Manufacturing - Peabody, MA

Michael Page
Peabody, MA, US
Full-time
We are sorry. The job offer you are looking for is no longer available.

This position involves assessing and ensuring compliance with quality standards throughout the manufacturing process, utilizing various auditing techniques to identify areas for improvement.

The auditor will collaborate with cross-functional teams to implement corrective actions and enhance overall product quality and operational efficiency.

Client Details

The Client is a global leader in high-precision, sensor-based technology and critical insight solutions, focusing on enhancing process safety and performance in the plastics, oil, and gas industries.

Serving a diverse customer base worldwide, the company has over six decades of experience providing tools and services that offer visibility into polymer processes, helping customers maintain consistency across locations.

Their portfolio includes cutting-edge sensing and polymer testing equipment that delivers highly accurate data for measuring polymer rheology, pressure, and temperature.

As part of a strategic plan to aggressively expand over the next five years, the company is seeking top talent to shape the future of sustainability in plastics production.

Description

  • Responsible for managing quality systems certified to ISO 9001 and ISO 17025 standards.
  • Acted as the designated representative for all ISO certification matters.
  • Extensive experience securing and maintaining hazardous product approvals (such as explosion-proof, flame-proof, and intrinsic safety) across various global regions including North America, Europe, and Asia.
  • Led efforts to ensure compliance with regulations governing high-concern substances like ROHS, REACH, and others, while ensuring company leadership stays informed and compliant.
  • Proficient in reading and interpreting technical drawings, with exposure to 2D / 3D CAD and PCB layout a plus.
  • Dedicated to staying informed of regulatory updates and leading proactive responses to mitigate risks and ensure continued compliance.
  • Managed and maintained Controlled Document Lists (CDLs), overseeing document revisions as necessary.
  • Developed templates and procedures for product certifications, ensuring alignment with company workflows.
  • Focused on improving efficiency in product certification and audit processes.
  • Created, implemented, and tracked key performance indicators (KPIs) for quality metrics.
  • Led and coordinated internal, external, and customer audits, including those conducted by certification bodies.
  • Controlled Engineering Change Orders (ECOs) and ensured timely implementation of changes.
  • Prepared, updated, and maintained all necessary documentation for the quality system.
  • Responsible for hiring, training, and supervising a small team (2-4 employees).
  • Oversaw the company's training record management platform.
  • Travel of up to 10% may be part of the role.

Profile

  • Must be legally authorized to work in the United States.
  • Minimum of 3-5 years in quality auditing, process auditing, or related fields.
  • Bachelor's degree in Engineering, Quality Management, or a related field preferred.
  • Hold certifications such as VDA 6.3, ISO9001, or other relevant auditing certifications are a plus.
  • Strong understanding of process control, quality management systems, and regulatory standards.
  • Proficiency with tools like Six Sigma, 8D, or other continuous improvement methodologies.
  • Excellent verbal and written communication skills for report writing and collaboration with cross-functional teams.
  • Strong analytical and problem-solving abilities to identify process inefficiencies and non-compliance.

Job Offer

  • Professional Growth : The role offers the opportunity to work with advanced quality management systems and auditing standards, enhancing expertise in process control and regulatory compliance.
  • Impact : By identifying inefficiencies and driving continuous improvement, the auditor can make a tangible impact on operational performance.
  • Cross-Functional Collaboration : The role involves working with diverse teams, providing exposure to different aspects of the business, fostering leadership and communication skills.
  • Innovative Environment : The company fosters a culture of innovation and problem-solving, ideal for those who enjoy developing and refining processes in dynamic settings.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law.

MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

16 hours ago
Related jobs
Michael Page
Peabody, Massachusetts

Minimum 2 years' experience in Quality Engineering, Quality Assurance, Manufacturing Engineering, or Design Engineering. In a small company environment, tasks include QMS implementation, interacting with operations and production, ensuring quality steps are followed, analyzing product returns, and a...

Michael Page
Danvers, Massachusetts

At least 2 years of experience in Quality Engineering, Quality Assurance, Manufacturing Engineering, or Design Engineering is necessary. Manage customer complaints regarding product quality. Develop manufacturing processes based on product specifications and research. Prior experience with Quality P...

Promoted
Draper Labs
Cambridge, Massachusetts

As a Senior System Quality Engineer, you will ensure that products meet the highest quality standards. Requires 5-7 years experience in quality engineering or other engineering role. From military defense and space exploration to biomedical engineering, lives often depend on the solutions we provide...

Promoted
PanelClaw
North Andover, Massachusetts

Software Quality Assurance Analyst. Perform regular Quality Assurance (QA) activities including: direct support to developers, verifying release candidates through multiple phases of testing and communicating all findings to stakeholders in real time. Skilled in documentation review and evaluating p...

Promoted
Elektrofi Inc
Boston, Massachusetts

Reporting to the Director of Technical Quality Assurance, the Manager, Quality Operations will play a pivotal role in ensuring the quality and compliance of Elektrofi programs from development through to commercialization. This position involves closely working with the Technical Development and Int...

Promoted
Arcaea
Boston, Massachusetts

Arcaea is seeking an experienced Quality Assurance Specialist to join our team and play a critical role in developing our ingredient toolset for the beauty and personal care industry. Author, review and approve Standard Operating Procedures (SOPs), Quality Risk Assessments (QRAs), Quality Plans rela...

Promoted
Berkshire Hathaway Specialty Insurance
Boston, Massachusetts

In this role, you will actively engage and work with offshore-based consulting partners in executing our quality assurance policy and claims activities. We have an exciting, entry-level opportunity to join our Boston office as an Associate QA Analyst within the IT team. The Associate QA Analyst is e...

Promoted
Vericel Corporation
Burlington, Massachusetts

The Quality Operations (QAOps) Manager oversees the quality compliance activities associated with the day-to-day Quality Operations which includes CMO relationships. Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity ...

Promoted
Northeast Family Services
Boston, Massachusetts

Northeast Family Services is looking for an experienced Electronic Health Record Quality Assurance Specialist to join our growing team. Acts as project coordinator for all Clinical Quality related projects such as establishing KPIs, Quality Assurance Plans, monitoring, and reporting on compliance. E...

Promoted
Nanobiosym
Cambridge, Massachusetts

The CLIA (Clinical Laboratory Improvement Amendments) Quality Manager will provide quality and compliance oversight to the Nanobiosym diagnostic testing laboratory. The CLIA Quality Manager will collaborate with direct and/or delegated authority to ensure the CLIA Quality Management Systems (QMS) ar...