Senior QA Manager Salary in Arcola, Mississippi

(Hiring Immediately) Part/Full-Time Security Officer Jobs Available in Arcola, MS. No Experience Required.

Title : Supplier Quality Engineer Location: Cleveland, MS. ONSITE. Duration: 6 months with the possibility of extension/conversion Need help with remediation efforts and to backfill one other team member Transitioning from paper based process to electronic system (Trackwise). Makes sure all assessments are completed - There are 180 records in process Trackwise is ideal, Any other similar Electronic based supplier process system would work 3-5 years in supplier process Experience in change control, Assessments. Onsite 5 days a week. Willing to look at relocation candidates Pharma industry is highly preferred but willing to look at candidates from any manufacturing industry Possibility for extension but conversion is not possible at this time Bachelor's degree is critical Interview process - Interview with Blossom and one other team managers. Virtual interview Responsibilities: • Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485 and ISO 9000

The Assembler will work on production equipment, not automated, such as RF Sealer and will assist the production areas in various tasks including sorting, counting, 6S activities, replenishing supplies, organizing stock, hanging blades, and assignments. May serve as a backup to other positions at the direction of management; other duties as assigned. Duties and Responsibilities Work on non-automated equipment such as RF Sealer and other kitting functions Perform work per work instructions and area metrics Keep work area clean by disposing empty boxes and cardboard, as well as keeping material Inform proper personnel of material shortage Train others in all areas Adhere to all safety requirements in the work area Practice 6S Knowledge, Skills and Abilities Understand and follow verbal and written instructions Basic math skills Work well with others Education and Experience Requirements High school diploma or equivalent Physical and Weight Lifting Demands The physical and weight lifting

Akkodis is seeking a Supplier Quality Engineer for a contract position with a client located in Cleveland, OH. The successful candidate will play a pivotal role in Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485 and ISO 9000. You will also work with suppliers to find solutions to identified problems/ Pay/Salary Range: $50.00/hr - $57.00/hr Supplier Quality Engineer job responsibilities include: • Create written reports and communicate the results clearly and effectively to the auditee and Baxter management. • Manage and insure timely implementation of supplier Corrective Action Reports (SCARs). • Provide engineering support for nonconforming material (NMR) and Return Material Authorization (RMA) issues. • Remediate Supplier files to support current and business development activity related to acquisition of new QUALIFICATIONS: • B.S Degree in Engineering required • Five years qualifying experience, including previous experience with qual

Job Description: Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485 and ISO 9000. Works with suppliers to find solutions to identified problems. Create written reports and communicate the results clearly and effectively to the auditee and management. Manage and insure timely implementation of supplier Corrective Action Reports (SCARs). Provide engineering support for nonconforming material (NMR) and Return Material Authorization (RMA) issues. Remediate Supplier files to support current and business development activity related to acquisition of new businesses. Remediate SNC Process, Verify supplier files are maintained and documented appropriately. Provide supplier metrics to management. Lead the supplier approval process by assessing manufacturing, Quality Systems capabilities and risks. Develop Improvement plans for Critical to quality suppliers. Manages personnel to maintain and reduce the Incoming Inspection cycle time. Establishes prob

Responsibilities: Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485 and ISO 9000. Works with suppliers to find solutions to identified problems. Create written reports and communicate the results clearly and effectively to the auditee and Baxter management. Manage and insure timely implementation of supplier Corrective Action Reports (SCARs). Provide engineering support for nonconforming material (NMR) and Return Material Authorization (RMA) issues. Remediate Supplier files to support current and business development activity related to acquisition of new businesses. Remediate SNC Process, Verify supplier files are maintained and documented appropriately. Provide supplier metrics to management. Lead the supplier approval process by assessing manufacturing, Quality Systems capabilities and risks. Develop Improvement plans for Critical to quality suppliers. Manages personnel to maintain and reduce the Incoming Inspection cycle time. Establis