Supplier Quality Engineer II Fresenius USA Manufacturing Inc. a Fresenius Medical Care N.A. company Lexington MA (Remote)
Job Duties:
Responsible for assuring End-to-End quality and sustainability with allocated supply base validating and releasing components and supporting the definition and implementation of supplier quality functional excellence initiatives. Specific duties include:
- Interfacing directly with suppliers to follow up on quality and performance issues managing Supplier Corrective Action Requests.
- Performing on-site and remote supplier quality audits for new suppliers participating in supplier approval process.
- Documenting and following up on audit results and required actions to be addressed by the supplier.
- Tracking analyzing and reporting on supplier performance metrics to stakeholders within quality logistics and manufacturing management using the appropriate software tools.
- Performing problem analysis process and machine capability studies as required and determining and proposing statistical process controls for appropriate suppliers processes.
- Collaborating with stakeholders to define deliverables meeting user needs and acceptance criteria.
- Ensuring documentation is aligned with corporate standards including FMEA DFMEA Manufacturing Process Characterization / PFMEA product life cycles.
- Performing gap analysis of Design Control Quality System determined changes required to close gaps and implement changes.
- Preparing Supplier Corrective Action Reports (SCARs) and Supplier Nonconformance Reports (SNCs) interfacing with both internal customers and the supply base to ensure effective actions are taken to reach closure.
- Execute Supplied Part Approval Process including providing supplier with required deliverables then reviewing and approving these deliverables.
- Review and update Supplier Quality SOPs using Quality tools and principles.
Requirements:
Position requires either a Bachelors degree (or an equivalent foreign degree) in Industrial Engineering Pharmaceutical Engineering Pharmacy or a related life sciences field and 5 years of experience as a Quality Engineer working in the medical device or pharmaceutical sector or alternatively a Masters degree(or an equivalent foreign degree) in Industrial Engineering Pharmaceutical Engineering Pharmacy or a related life science field and 3 years of experience as a Quality Engineer working in the medical device or pharmaceutical sector. Must also have had 3 years of experience (which can have been gained concurrently with either of the primary experience requirements above) working with the following:
- Performing on-site and remote supplier quality audits and participating in the supplier selection and approval process;
- Tracking analyzing and reporting supplier performance metrics to internal stakeholders within quality logistics and manufacturing management using the appropriate software tools;
- Maintaining Risk Management files including Hazard analysis Design FMEA Use FMEA and Process FMEA for assigned product families;
- Utilizing Root Cause Analysis concepts to investigate issues and implement Corrective and Preventive actions including effectiveness checks.
- Performing Design of Experiments (DoE) using Minitab and analyzing various process parameters with the use of statistical tools (SPC) such as Gage R & R Gage linearity and Bias study interaction plot process capability study to optimize the blending and compression process.
This position requires approximately 10% domestic and international travel.
This is a telecommuting position working from home. May reside anywhere in the United States.
Salary is $163030 - $171181 per year for a 40-hour work week.
EOE disability/veterans
Supplier Quality Engineer II Fresenius USA Manufacturing Inc. a Fresenius Medical Care N.A. company Lexington MA (Remote) Job Duties:Responsible for assuring End-to-End quality and sustainability with allocated supply base validating and releasing components and supporting the definition and impleme...
Supplier Quality Engineer II Fresenius USA Manufacturing Inc. a Fresenius Medical Care N.A. company Lexington MA (Remote)
Job Duties:
Responsible for assuring End-to-End quality and sustainability with allocated supply base validating and releasing components and supporting the definition and implementation of supplier quality functional excellence initiatives. Specific duties include:
- Interfacing directly with suppliers to follow up on quality and performance issues managing Supplier Corrective Action Requests.
- Performing on-site and remote supplier quality audits for new suppliers participating in supplier approval process.
- Documenting and following up on audit results and required actions to be addressed by the supplier.
- Tracking analyzing and reporting on supplier performance metrics to stakeholders within quality logistics and manufacturing management using the appropriate software tools.
- Performing problem analysis process and machine capability studies as required and determining and proposing statistical process controls for appropriate suppliers processes.
- Collaborating with stakeholders to define deliverables meeting user needs and acceptance criteria.
- Ensuring documentation is aligned with corporate standards including FMEA DFMEA Manufacturing Process Characterization / PFMEA product life cycles.
- Performing gap analysis of Design Control Quality System determined changes required to close gaps and implement changes.
- Preparing Supplier Corrective Action Reports (SCARs) and Supplier Nonconformance Reports (SNCs) interfacing with both internal customers and the supply base to ensure effective actions are taken to reach closure.
- Execute Supplied Part Approval Process including providing supplier with required deliverables then reviewing and approving these deliverables.
- Review and update Supplier Quality SOPs using Quality tools and principles.
Requirements:
Position requires either a Bachelors degree (or an equivalent foreign degree) in Industrial Engineering Pharmaceutical Engineering Pharmacy or a related life sciences field and 5 years of experience as a Quality Engineer working in the medical device or pharmaceutical sector or alternatively a Masters degree(or an equivalent foreign degree) in Industrial Engineering Pharmaceutical Engineering Pharmacy or a related life science field and 3 years of experience as a Quality Engineer working in the medical device or pharmaceutical sector. Must also have had 3 years of experience (which can have been gained concurrently with either of the primary experience requirements above) working with the following:
- Performing on-site and remote supplier quality audits and participating in the supplier selection and approval process;
- Tracking analyzing and reporting supplier performance metrics to internal stakeholders within quality logistics and manufacturing management using the appropriate software tools;
- Maintaining Risk Management files including Hazard analysis Design FMEA Use FMEA and Process FMEA for assigned product families;
- Utilizing Root Cause Analysis concepts to investigate issues and implement Corrective and Preventive actions including effectiveness checks.
- Performing Design of Experiments (DoE) using Minitab and analyzing various process parameters with the use of statistical tools (SPC) such as Gage R & R Gage linearity and Bias study interaction plot process capability study to optimize the blending and compression process.
This position requires approximately 10% domestic and international travel.
This is a telecommuting position working from home. May reside anywhere in the United States.
Salary is $163030 - $171181 per year for a 40-hour work week.
EOE disability/veterans
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