Senior Quality Manager

Full Time
Beverly, MA
Posted
Job description

We are searching for a Senior Quality Manager for an amazing client in Beverly.

Our client engineers and manufactures precision servo actuators, gearheads and gear component sets.

This is a direct hire opportunity.

The Senior Quality Manager has responsibility for leading Quality Engineering, Supplier quality, Metrology, Final Inspection, and Calibration ensuring compliance and supporting continuous improvement.

The Quality Manager will partner closely with Quality Assurance, Procurement and Operations to ensure that the quality management system is designed, established, and effectively deployed at all levels of the organization, in compliance with Harmonic Drive quality standards and applicable regulatory standards.

The Senior Quality Manager is tasked with the obligation to ensure all company products meet customer expectations and demands. Specific daily duties for this position include overseeing employee performance and inspecting products to ensure conformity throughout the machining and assembly process. Where products fail to meet quality standards, the quality manager is responsible for discarding and rejecting the product and documenting the reasons why it failed to meet the quality standards.

Essential Functions

· Deploy quality and compliance strategies for the site in line with industry quality standards and strategic direction.

· Lead problem solving and root cause analysis activities with manufacturing staff and suppliers to eliminate recurrence of non‐conformances.

· Apply systematic problem-solving methodologies in resolving quality issues.

· Be an effective member of the Leadership Team, enforce compliance and foster continuous quality improvements.

· Escalate unexpected data/trends and risks appropriately, and drive/support resolution

· Generate and present metrics for QC stability in support of management review and investigations

· Initiation and completion of necessary change controls, deviations, and engineering investigation reports

· Ensure all products are tested and released on time and in compliance with current regulatory and quality requirements.

· Assure that manufacturing processes are properly developed, qualified, and validated to ensure the highest possible quality.

· Oversee the development and implementation of quality training programs; provide expertise and guidance to managers and employees of the site.

· Establish documented methods for part inspection and evaluation.

· Supervise staff and monitoring production standards

· Monitor, communicate and work with purchasing to improve supplier quality performance.

· Manage Risk Management implementation, monitoring, and control

· Oversee completion of MRB, CAPA, FMEA, SPC, Change management, and other quality requirements

· Promote a culture of Quality and excellence

Competencies:

· Knowledge and experience with ISO 9001, AS9100, and ISO 13485 standards.

· Regulatory, legal, statutory, and other industry related environmental compliance knowledge

· Working knowledge of metrology equipment and ability to read and interpret drawings and GD&T.

· Competent leading problem solving, root cause analysis and corrective action activities.

· Strong ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations.

· Highly collaborative, with excellent organizational, communication (written and verbal), and interpersonal skills

· Application of Six Sigma / 8D methodologies to eliminate defects.

· Ability to build strong and collaborative relationships with management, peers and direct reports.

· Possess strong organizational skills and is detailed oriented.

· Able to function independently of direct supervision.

· Advanced computer skills using Microsoft Office applications, Minitab or other suitable software tools for statistical analysis.

· Possess strong conflict management and negotiation skills.

Required Education and Experience:

· B.S. in engineering, quality or related discipline required, advanced degree preferred.

· 10+ years of experience in either manufacturing production, aerospace, medical devices, or similar regulated industry environment, with 5+ years of experience in a GMP Quality Assurance function and experience managing teams

· Leads audit and inspection, preparation, resolution of audits and inspection findings and liaises with audit group and third-party inspectors through stages of the audits. Prepares report and necessary documentation (corrective and preventive actions) and provides to applicable stakeholders for internal, external and certification audits.

· Six Sigma Black Belt strongly preferred

Masis Staffing ensures peak service to its clients through our culture, experience, and ethics. We are a family-oriented, service-driven staffing firm with a sincere and responsible team dedicated to delivering custom solutions for all our client hiring needs. Our associates are the heart of every client solution and are a key asset to the continued development of our partnerships. Masis is known for the great care we take with employees and clients alike!

For information on Masis Staffing, including more information on employee benefits and our company culture, visit our website at www.masisstaffing.com.

Masis Staffing is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Job Type: Full-time

Pay: $120,000.00 - $140,000.00 per year

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Parental leave
  • Vision insurance

Schedule:

  • 8 hour shift
  • Monday to Friday

Work Location: In person

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