Quality Management Specialist role owning and improving the quality management system for an industrial valve manufacturer, ensuring components and fittings meet standards, customer specs and production goals. You’ll lead audits, corrective actions, RMAs and act as the main liaison for customer/vendor inspections. Standout perks include tuition reimbursement and a clean, safe, climate-controlled facility with modern equipment.
- Tuition reimbursement program
- 401k match up to 6%
- Generous PTO and 10 holidays
CPV Manufacturing, an industrial valve manufacturer located in Kennett Square, PA, is looking for a Quality Management Specialist to join our team. This position develops implements and manages quality systems designed to ensure conformity in the manufacture of valve components and pipe/tube fittings consistent with established standards, customer specifications and production goals. We offer a tuition reimbursement program, a clean, safe, climate-controlled facility with modern equipment and much more! Other benefits include a comprehensive medical and dental plan, matching 401k, generous PTO program and 10 paid holidays.
Essential Duties and Responsibilities:
- Works directly with third party inspectors in relation to source inspections
- Acts as Technical Resource for others
- Participates in Material Review Board
- Responsible for conducting and managing internal quality audits
- Manages Return Material Authorizations (RMA's)
- Manages customer complaints and corrective actions
- Acts as the Company liaison and main contact for customer and vendor audits
- Ensures that quality system requirements are maintained and reported
- Evaluates current ISO procedures and practices, and develops and implements improvements as needed
- Responsible for Internal Auditing as well as training internal auditors
- Develops and implements primary quality control systems consistent with standard operating procedures
- Manages risk register
- Directs and coordinates analysis of products in compliance with regulations and procedures
- Reviews all data generated in support of method validation and stability studies
- Oversees completion of appropriate documentation to support testing procedures
- Ensures quality/laboratory equipment is maintained in accordance with established schedules and procedures
- Owner of the Radiation Protection Program - managing training records and state registration of equipment
- Responsible for ISO training for all new employees
- Customer compliant paperwork
- Performs other related duties as assigned by management
Qualifications
- Education: Bachelor's degree in a related field.
Experience
5+ years of related experience
Skills
- Problem solving and attention to detail
- Customer service oriented
- Planning and organizing
- Teamwork
- Good Communicator
- Proficient in Microsoft Office Suite
Physical Requirements and Working Conditions:
- Work environment is in the primarily in the office
- Ability to sit or stand for long periods of time
Benefits
- Competitive salary commensurate on experience
- generous paid time off plan and 10 paid holidays
- 401k match up to 6%
- Major medical and dental insurance as well as company-paid Short Term Disability and Life Insurance