What are the responsibilities and job description for the Quality Manager position at Girouard Tool Corp?
Overview
We are seeking a dedicated and experienced Quality Manager to oversee and enhance our quality management systems. The ideal candidate will be responsible for ensuring compliance with industry standards and regulations, including FDA regulations and ISO 9001 & 13485. This role requires a strong focus on quality control, project management, and the ability to analyze data to drive continuous improvement within our organization.
Responsibilities
- Main point of contact with customers, regulatory, and government agencies on all quality-related issues and audits.
- Conduct regular quality audits to ensure compliance with internal policies and external regulations.
- Collaborate with cross-functional teams to identify areas for improvement in processes and products.
- Analyze data related to product quality and performance, providing insights for decision-making.
- Lead department in continuous improvement activities, preventative actions, root cause analysis, and corrective actions in support of the Quality System and effective operational execution.
- Manage projects related to quality initiatives, ensuring timely completion and adherence to specifications.
- Maintains and improves product quality by completing product, company, systems, compliance, and surveillance audits; investigating customer complaints, manufacturing, and training methods.
- Implement measures to improve inspection methods, equipment/tool performance, product quality, efficiency, and morale.
- Ensure full compliance with company policies and procedures.
- Ensure materials meet specifications and quality standards and are cost-efficient.
Skills
- Bachelor's degree and a minimum of 5 years of proven quality management, or a combination of education and experience.
- Strong project management skills with the ability to lead cross-functional teams effectively.
- Proficient in Microsoft Office Applications (Excel, Word, etc., Outlook, Access).
- Strong familiarity with ISO compliance.
- Training as ISO9001/AS9100 Lead Auditor/ISO 13485.
- Proven experience in statistical analysis and data analysis.
- Ability to multitask and prioritize tasks with strict deadlines.
- Proficient in analyzing data to identify trends, issues, and opportunities for improvement.
- Familiarity with FDA regulations relevant to our industry.
- Extensive experience in quality control processes and methodologies.
- Knowledge of ISO 13485 standards and their application in a manufacturing environment.
- Effective communication skills (verbal and written).
- Strong leadership and people skills.
- Excellent planning, organizational, and decision-making skills.
- Must have solid skills in leadership, presentation, communication, and customer service
- Must have experience in the manufacturing and production industry, specifically in Quality Control and injection molding.
- Must have a working knowledge of metrology equipment, usage, and calibration.
- Ability to lead, motivate, coach, and teach others.
- Experience conducting quality audits and implementing corrective actions as necessary.
Join our team as a Quality Manager where your expertise will play a crucial role in maintaining the highest standards of product quality and safety within our organization.
Job Type: Full-time
Pay: $84,014.00 - $88,844.00 per year
Benefits:
- 401(k) matching
- Health insurance
Schedule:
- Day shift
- No nights
- No weekends
Ability to Commute:
- Leominster, MA 01453 (Required)
Work Location: In person
Salary : $84,014 - $88,844