Quality Supervisor - Medical Device Manufacturing

Location: Philadelphia
Posted on: June 23, 2025

Job Description:

Are you a Quality Supervisor who has at least 3 years of experience working as a Quality Control Inspector? Do you have experience working with ISO 13485 and ISO 9001? Do you have a Metrology and/or CNC Programmer background? Do you have a strong understanding of First Article Inspections (FAI's)? If so, please read on and apply to the Quality Supervisor - Medical Device Manufacturing job based near Philadelphia, PA. Client Details We are currently partnered up with a growing Medical Device Manufacturing company in their search to add a Quality Supervisor to the team due to growth. This Quality Supervisor will lead a team of quality inspectors and will be offered 100% employer paid medical benefits. The ideal candidate will have 3 years of experience in a Quality Control Inspector role, supervisory experience, strong understanding of FAI's, and ISO 13485 experience. If interested, please read on and apply to the Quality Supervisor - Medical Device Manufacturing job based just West of Philadelphia, PA. Description The Quality Supervisor - Medical Device Manufacturing will be responsible for the following: Assisting in maintaining ISO 9001 and 13485 Medical Device Quality Management System compliance. Perform First Article Inspections, (FAI's). FAI's must be performed in a timely manner throughout the day. No open FAIs are to remain at the end of the shift. Responsible for writing inspection plans for manufacturing cells for input into proprietary inspection software. Work with Management to develop specific and measurable goals, improvements and standards to continuously and consistently improve quality and reduce errors. Act on behalf of the customer to audit and maintain the accuracy and timely delivery of products. Make sure that roving inspections are done at all workstations on a routine daily basis and results are reported back to the machinist and cell Manager. Inspect materials, products, and equipment to find defects and implement corrections. Lead by example in performing FAI's and roving inspections. Generate Non-Conforming Reports, (NCR's), to notify employees of production errors. Make certain that those involved are trained so as to avoid a repetition of previous mistakes. Assists in the maintenance and calibration and traceability of gages and other inspection equipment. Maintain the compliance and accuracy of all data entered into system Control, maintain and keep an accurate inventory of all Inspection equipment. Observe work, and monitor measurements, data, and other indicators to ensure operators comply with processing standards. Assist employees with the interpretation of blueprints and with the analysis of parts according to those prints. Notify employees of quality related errors and how they can be corrected. Train new employees on the inspection software. Ensures that all Trainings assigned to employees in the cell are completed in a timely manner. Train new employees on the efficient and proper use of inspection tools and machines, including but not limited to, calipers, gauges, micrometers, and comparators. Guide new employees through the inspection process. Profile The ideal Quality Supervisor - Medical Device Manufacturing will have the following qualifications: 3 years of experience ideally within a Quality Control Inspection based role ISO 13485 and ISO 9001 experience Experience with CNC Programming Strong Knowledge base of Metrology Strong Knowledge base of First Article Inspections (FAI's) Supervisor experience preferred but previous mentorship would be considered Ideally a Bachelor's degree in an Engineering related field but open to Associates and/or High School Diploma's if the work experience lines up Job Offer The successful Quality Supervisor - Medical Device Manufacturing will be rewarded with the following: Base Salary of $60,000-$85,000 depending on experience Bonus 100% Employer Paid Medical Benefits PTO 401K Match Relocation Assistance 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.

Keywords: , West New York , Quality Supervisor - Medical Device Manufacturing, Engineering , Philadelphia, New Jersey