.. chance to make a difference in the lives of patients Key responsibilities: Administer radiation therapy to patients as prescribed by a radiation oncologist Maintain accurate records of treatment sessions and patient progress Monitor and assess patient reactions to radiation therapy Collaborate with the .. read more
Job Description
Job Description
JOB SUMMARY This position is primarily responsible for performing receiving, first piece, in-process and final inspection or test on a wide variety of parts and document results. Indicate inspection status, maintain product traceability and non-conforming material control. Participate in internal audits, statistical process control and assist control of process documentation, records, and equipment calibration.
ESSENTIAL RESPONSIBILITIES Inspect, measure and/or test incoming parts, production first piece, in-process and final product, record results and notify appropriate personnel. Indicate inspection status of parts with assigned labels and stamps. Maintain product identification and traceability. Control non-conforming product in accordance with documented procedures and verify timely corrective and preventative action. Protect product during handling and storage in the performance of work. Monitor factory environmental conditions, record data and alert adverse conditions. Assist with distribution and control of process documentation and quality records. Assist with control of measuring and test equipment calibration. Participate in internal quality audits to verify compliance with documented procedures and specifications, record results and verify audit corrective action. Assist with statistical methods of verifying and controlling process capability. Provide input when required to quality planning for specific projects and products. Provide leadership to production personnel on quality issues. Comply with and reinforce the requirements of the Cirtec Quality System Manual and Standard Operating Procedures, ISO 9002, FDA Quality System Regulations, and other customer standards. Follow Occupational Safety and Health regulations, including laser safety practices. Other agreed duties within the Quality Department consistent with training, qualification, and experience. Provide Quality Support for the disposition of discrepant material. Provide leadership to production personnel in relation to quality. Provide Quality Control support to Manufacturing & Engineering. Reliable, consistent, and punctual attendance is an essential function of the job. Complies with company, quality, and safety standards, policies, and procedures. Other duties as assigned.
This is not a remote position. An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
QUALIFICATIONS High school diploma or General Education Degree (GED) is required. 1+ years’ experience in medical device industry and manufacturing required. Certificate/s of training related to this field of work (medical or quality assurance). 3 years’ experience as a Quality Control Inspector. Proven experience in inspection and documenting results. Able to demonstrate competence in interpreting technical drawings & specifications. Proficient in the use of microscopes, measuring and test equipment. Must be able to read, write and speak fluent English. Able to check dimensions, squareness, hole locations, surface relationships, finish material defects and mechanical strength of product following appropriate training. Have experience in the use of PC’s and Microsoft Office software applications. Brooklyn Park Additional Qualifications: · Prefer experience and familiarity with operations such as cleanroom manufacturing, swiss machining, milling, stamping, laser cutting, laser welding, coiling, crimping, swaging, adhesive bonding/backfill, liquid silicone & thermoplastic injection molding, annealing, and general mechanical assembly.
WORKING ENVIRONMENT Work is performed in a manufacturing environment. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.
EEO STATEMENT Cirtec Medical Corporation is an Equal Opportunity
Minority/Female/Individuals
with
Disabilities/Protected
Veteran and Affirmative Action Employer Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.
#J-18808-Ljbffr
Job Description
JOB SUMMARY This position is primarily responsible for performing receiving, first piece, in-process and final inspection or test on a wide variety of parts and document results. Indicate inspection status, maintain product traceability and non-conforming material control. Participate in internal audits, statistical process control and assist control of process documentation, records, and equipment calibration.
ESSENTIAL RESPONSIBILITIES Inspect, measure and/or test incoming parts, production first piece, in-process and final product, record results and notify appropriate personnel. Indicate inspection status of parts with assigned labels and stamps. Maintain product identification and traceability. Control non-conforming product in accordance with documented procedures and verify timely corrective and preventative action. Protect product during handling and storage in the performance of work. Monitor factory environmental conditions, record data and alert adverse conditions. Assist with distribution and control of process documentation and quality records. Assist with control of measuring and test equipment calibration. Participate in internal quality audits to verify compliance with documented procedures and specifications, record results and verify audit corrective action. Assist with statistical methods of verifying and controlling process capability. Provide input when required to quality planning for specific projects and products. Provide leadership to production personnel on quality issues. Comply with and reinforce the requirements of the Cirtec Quality System Manual and Standard Operating Procedures, ISO 9002, FDA Quality System Regulations, and other customer standards. Follow Occupational Safety and Health regulations, including laser safety practices. Other agreed duties within the Quality Department consistent with training, qualification, and experience. Provide Quality Support for the disposition of discrepant material. Provide leadership to production personnel in relation to quality. Provide Quality Control support to Manufacturing & Engineering. Reliable, consistent, and punctual attendance is an essential function of the job. Complies with company, quality, and safety standards, policies, and procedures. Other duties as assigned.
This is not a remote position. An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
QUALIFICATIONS High school diploma or General Education Degree (GED) is required. 1+ years’ experience in medical device industry and manufacturing required. Certificate/s of training related to this field of work (medical or quality assurance). 3 years’ experience as a Quality Control Inspector. Proven experience in inspection and documenting results. Able to demonstrate competence in interpreting technical drawings & specifications. Proficient in the use of microscopes, measuring and test equipment. Must be able to read, write and speak fluent English. Able to check dimensions, squareness, hole locations, surface relationships, finish material defects and mechanical strength of product following appropriate training. Have experience in the use of PC’s and Microsoft Office software applications. Brooklyn Park Additional Qualifications: · Prefer experience and familiarity with operations such as cleanroom manufacturing, swiss machining, milling, stamping, laser cutting, laser welding, coiling, crimping, swaging, adhesive bonding/backfill, liquid silicone & thermoplastic injection molding, annealing, and general mechanical assembly.
WORKING ENVIRONMENT Work is performed in a manufacturing environment. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.
EEO STATEMENT Cirtec Medical Corporation is an Equal Opportunity
Minority/Female/Individuals
with
Disabilities/Protected
Veteran and Affirmative Action Employer Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.
#J-18808-Ljbffr