Quality Supervisor – Medical Device Manufacturing Position Available In Philadelphia, Pennsylvania

Job Description:

Are you a Quality Supervisor who has at least 3 years ofexperience working as a Quality Control Inspector? Do you haveexperience working with ISO 13485 and

ISO 9001?

Do you have aMetrology and/or CNC Programmer background? Do you have a strongunderstanding of First Article Inspections (FAI’s)? If so, pleaseread on and apply to the Quality Supervisor•Medical DeviceManufacturing job based near Philadelphia, PA. Client Details Weare currently partnered up with a growing Medical DeviceManufacturing company in their search to add a Quality Supervisorto the team due to growth. This Quality Supervisor will lead a teamof quality inspectors and will be offered 100% employer paidmedical benefits. The ideal candidate will have 3 years ofexperience in a Quality Control Inspector role, supervisoryexperience, strong understanding of FAI’s, and ISO 13485experience. If interested, please read on and apply to the QualitySupervisor•Medical Device Manufacturing job based just West ofPhiladelphia, PA. Description The Quality Supervisor•MedicalDevice Manufacturing will be responsible for the following:

Assisting in maintaining ISO 9001 and 13485 Medical Device QualityManagement System compliance. Perform First Article Inspections,(FAI’s). FAI’s must be performed in a timely manner throughout theday. No open FAIs are to remain at the end of the shift.

Responsible for writing inspection plans for manufacturing cellsfor input into proprietary inspection software. Work withManagement to develop specific and measurable goals, improvementsand standards to continuously and consistently improve quality andreduce errors. Act on behalf of the customer to audit and maintainthe accuracy and timely delivery of products. Make sure that rovinginspections are done at all workstations on a routine daily basisand results are reported back to the machinist and cell Manager.

Inspect materials, products, and equipment to find defects andimplement corrections. Lead by example in performing FAI’s androving inspections. Generate Non-Conforming Reports, (NCR’s), tonotify employees of production errors. Make certain that thoseinvolved are trained so as to avoid a repetition of previousmistakes. Assists in the maintenance and calibration andtraceability of gages and other inspection equipment. Maintain thecompliance and accuracy of all data entered into system Control,maintain and keep an accurate inventory of all Inspectionequipment. Observe work, and monitor measurements, data, and otherindicators to ensure operators comply with processing standards.

Assist employees with the interpretation of blueprints and with theanalysis of parts according to those prints. Notify employees ofquality related errors and how they can be corrected. Train newemployees on the inspection software. Ensures that all Trainingsassigned to employees in the cell are completed in a timely manner.

Train new employees on the efficient and proper use of inspectiontools and machines, including but not limited to, calipers, gauges,micrometers, and comparators. Guide new employees through theinspection process. Profile The ideal Quality Supervisor•MedicalDevice Manufacturing will have the following qualifications: 3years of experience ideally within a Quality Control Inspectionbased role ISO 13485 and

ISO 9001

experience Experience with CNCProgramming Strong Knowledge base of Metrology Strong Knowledgebase of First Article Inspections (FAI’s) Supervisor experiencepreferred but previous mentorship would be considered Ideally aBachelor’s degree in an Engineering related field but open toAssociates and/or High School Diploma’s if the work experiencelines up Job Offer The successful Quality Supervisor•MedicalDevice Manufacturing will be rewarded with the following: BaseSalary of $60,000•85,000 depending on experience Bonus 100%Employer Paid Medical Benefits

PTO 401K

Match Relocation AssistanceMPI does not discriminate on the basis of race, color, religion,sex, sexual orientation, gender identity or expression, nationalorigin, age, disability, veteran status, marital status, or basedon an individual’s status in any group or class protected byapplicable federal, state or local law. MPI encourages applicationsfrom minorities, women, the disabled, protected veterans and allother qualified applicants.