Position Details
Quality Management Specialist Apply
Job Description
Summary:
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:
Qualifications:
Skills:
Physical Requirements and Working Conditions:
Benefits:
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:
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- Works directly with third party inspectors in relation to source inspections \n
- Acts as Technical Resource for others \n
- Participates in Material Review Board \n
- Responsible for conducting and managing internal quality audits \n
- Manages Return Material Authorizations (RMA's) \n
- Manages customer complaints and corrective actions \n
- Acts as the Company liaison and main contact for customer and vendor audits \n
- Ensures that quality system requirements are maintained and reported \n
- Evaluates current ISO procedures and practices, and develops and implements improvements as needed \n
- Responsible for Internal Auditing as well as training internal auditors \n
- Develops and implements primary quality control systems consistent with standard operating procedures \n
- Manages risk register \n
- Directs and coordinates analysis of products in compliance with regulations and procedures \n
- Reviews all data generated in support of method validation and stability studies \n
- Oversees completion of appropriate documentation to support testing procedures \n
- Ensures quality/laboratory equipment is maintained in accordance with established schedules and procedures \n
- Owner of the Radiation Protection Program - managing training records and state registration of equipment \n
- Responsible for ISO training for all new employees \n
- Customer compliant paperwork \n
- Performs other related duties as assigned by management \n
Qualifications:
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- Education: Bachelor's degree in a related field. \n
- Experience: 5+ years of related experience \n
Skills:
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- Problem solving and attention to detail \n
- Customer service oriented \n
- Planning and organizing \n
- Teamwork \n
- Good Communicator \n
- Proficient in Microsoft Office Suite \n
Physical Requirements and Working Conditions:
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- Work environment is in the primarily in the office \n
- Ability to sit or stand for long periods of time \n
Benefits:
- \n
- Competitive salary commensurate on experience \n
- generous paid time off plan and 10 paid holidays \n
- 401k match up to 6% \n
- Major medical and dental insurance as well as company-paid Short Term Disability and Life Insurance \n
