Quality Specialist
at GN Corporations
Airdrie, AB, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 15 Feb, 2025 | USD 75000 Annual | 18 Nov, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Specific duties, and responsibilities of the Quality Specialist shall include the following:
- Responsible for the organization, co-ordination, and direction of all quality related activities in accordance with customer requirements and the company Quality Program.
- Oversee the product manufacturing processes to ensure quality by supervising development of PFMEA and control plans through mistake proofing the critical failure modes.
- Review products, processes, and systems on an ongoing basis to determine where improvements can be made.
- Supervise the activities of all Quality Inspectors, Receiving Inspection and Supplier Quality Assurance.
- Work closely with all Internal Departments, Suppliers, and all Customers to ensure problem prevention and resolution.
- Responsible for the evaluation of statistical techniques and gather process relevant crucial data and develop techniques to reduce drift and control various processes.
- Assist the development and maintenance of advanced quality plans such as cost of quality programs to improve and reduce the cost of poor quality.
- Responsible for improved methods to move current quality objectives to the next level of performance.
- Determine quality metrics for all manufacturing procedures and Processes.
- Monitor the entire production cycle and perform regular inspections to identify potential malfunctions as early as possible.
- Prepare reports on defects trend analysis and propose corrective actions.
- Coordinate and manage the continual improvement process utilizing structured problem solving within the corrective and preventive action processes.
- Develop Quality Inspection Strategy by incorporating the Control Plan into the Manufacturing Inspection Reports and data collection for analysis.
- Be a core member for APQP (Advanced Product Quality Planning) activities, manage all quality related tasks during APQP stage.
- Prepare all Documents for customer requirements (included but limited to Quality Plan, PFMEA, Control Plans, SPC, MSA, Inspection Reports, Customer data packages etc.)
- PPAP submission based on customer specified submission level.
- IMDS (International Material Data System) approval and submission if required by customer.
- Conduct process capability analyses to evaluate manufacturing process performance compared to customer requirements.
Represent the Quality department for Pre-production meetings and communication open between Quality, Programs and Operations Team on the status of the process from a Quality standpoint.
- Ability to work with senior management team and implement their vision.
- Collaborate with Quality Analyst to successfully launch New Product to operations.
- Mentor and coach, the quality department to bring all resources to the level of knowledge required to effectively support the APQP and plant performance requirements.
- Assist in resolving process and product quality issues. Perform all work in accordance with quality standards and established safe work practices.
- Ensure that all findings are brought to the attention of the appropriate personnel.
- Verifies & validates processes and product conformance via Inspection Receiving, First Offs, Final Inspection, Process & Dock audits, testing.
- Identifies and records non-conformances, participates in the multidisciplinary GNs team to identify Root Cause, Corrective & Preventive Actions.
Responsibilities:
- Responsible for the organization, co-ordination, and direction of all quality related activities in accordance with customer requirements and the company Quality Program.
- Oversee the product manufacturing processes to ensure quality by supervising development of PFMEA and control plans through mistake proofing the critical failure modes.
- Review products, processes, and systems on an ongoing basis to determine where improvements can be made.
- Supervise the activities of all Quality Inspectors, Receiving Inspection and Supplier Quality Assurance.
- Work closely with all Internal Departments, Suppliers, and all Customers to ensure problem prevention and resolution.
- Responsible for the evaluation of statistical techniques and gather process relevant crucial data and develop techniques to reduce drift and control various processes.
- Assist the development and maintenance of advanced quality plans such as cost of quality programs to improve and reduce the cost of poor quality.
- Responsible for improved methods to move current quality objectives to the next level of performance.
- Determine quality metrics for all manufacturing procedures and Processes.
- Monitor the entire production cycle and perform regular inspections to identify potential malfunctions as early as possible.
- Prepare reports on defects trend analysis and propose corrective actions.
- Coordinate and manage the continual improvement process utilizing structured problem solving within the corrective and preventive action processes.
- Develop Quality Inspection Strategy by incorporating the Control Plan into the Manufacturing Inspection Reports and data collection for analysis.
- Be a core member for APQP (Advanced Product Quality Planning) activities, manage all quality related tasks during APQP stage.
- Prepare all Documents for customer requirements (included but limited to Quality Plan, PFMEA, Control Plans, SPC, MSA, Inspection Reports, Customer data packages etc.)
- PPAP submission based on customer specified submission level.
- IMDS (International Material Data System) approval and submission if required by customer.
- Conduct process capability analyses to evaluate manufacturing process performance compared to customer requirements
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Graduate
Proficient
1
Airdrie, AB, Canada