| | | 20,000+ Fresh Resumes Monthly | |
|
|
| | Related Resumes Equality control specialist, receptionist / costumer service. Plantation, FL Customer Service Quality Control Hollywood, FL R D Quality Control Pembroke Pines, FL Forklift Operator Quality Control Plantation, FL Customer Service Quality Control Doral, FL Control Specialist Internal Auditor,medical veterinaria, master Miami, FL Quality Assurance Inventory Control Miami, FL |
|
Click here or scroll down to respond to this candidateGhoufrane, MaraghiStreet Address
PHONE: PHONE NUMBER AVAILABLE EMAIL:EMAIL AVAILABLEWork experienceMagic Leap: (August30 2021, Present)Quality Control SpecialistInspect/measure/report on incoming materials, in process components, and outgoing products to confirm quality performance requirementsDetermine if products can be use and if they meet client specificationsCollaborate with Operations and Engineering on quality issues troubleshooting including guiding completion of root cause and corrective actionsPeform visual microscopic and metrology inspectionOperate measurement equipments by following operating and calibration instructionsMaintain continuous and stable level of visual inspection where requiredOwn outgoing quality metric for a factory and drive 8D process for customer failuresUse and test incoming using Metrology tool tropel measurementUse of microscopic VHX testing to make sure no defects on incoming material.Use of google sheet google slides to publish and track data.perform QCP Audit to make sure control plans are followed in production floor.lead investigation with engineering team supplier quality team and production team.Use of OGP optical gaging products to inspect incoming material or investigate optical issues related to performance of camera lenses in optical frames.Access to SAP system to complete transactions and release material to productionClean Room Associate:Responsible of the calibration of Micro- dispensing machine.Operate the alignment, the inspection and the assembly of finish products.Clean maintain and proper store micro-valves used in the machine.Responsible of performing tests and validation of finish product.Attending production meeting to discuss the plan and the schedule of the day.Creating and completing S6 projects to meet lean manifacturing standarsUsing google sheets, google slide, google document to report document and update production activities.Using digital documentation, obsolete the use of hard copies documentationUse MES system for Material and production tractability.Review Edit and create Work Instructions.Participate on engineering projects by running DOE (Designed Optical E engineering).KD Pharma: (July21 2020, August12 2021)Assistant supervisorResponsible for maintaining a positive work environment.Supervise employees performance at production floor (upstream and downstream).Report any production issues (Material, Machines/ Equipments and Personal) to high management.ensure the accuracy of all production batches.Responsible of daily review of batch records and computer entry in the system used.Performing training to production personel maintain and enforce valid updated trainings.Ensure CGMP and SOP requirements are recommended and followed.Responsible of daily auditing all production work areas and enforce 5S culture.Efficiently organize and lead the production area by example and professionalism.Secure and provide efficient flow information within all departments.Ability to inform, communicate, advise and support other departments heads and managers.have understanding and knowledge needed about safety SOPs and the requirements for the position to ensure a safer working environment. All precautions and processes must be adhered to in order to maintain a high level of safety complianceMagic leap:( March2019, April 2020) (fixtures technician)Perform task with a lot of Details to support the operation manufacturing line.communicate in a professional and courteous manner among inter-department staff, staff outside of the initial department.Active Participation in Safety.Participate in writing SOPs and Work instructions and check list.Rework/Repair/clean items for production line.Responsible of performing daily PM for equipment.Preventative Maintenance Quality.Process Improvement knowledge of Lean manufacturing, 5S, work place organization.Able to do corrective maintenance, control action/plans/troubleshooting.Noven pharmaceutical: (January,2019- march,2019)Perform all the general duties and operations to manufacture the Gel Patch product.Operate machines and handle components using prescribed standard operating procedures and cGMP guidelines.Ensure the product meets the quality requirements.Complete the necessary documentation and records to maintain quality control.Operate Gel Patch manufacturing equipment; Mixing, Coat/Cut, and Packaging.Perform manual operations when automated systems are inoperable.Blend various ingredients and package the product into components required for the Gel Patch product.Check and weigh components to ensure compliance.Clean and maintain production room and equipment.Perform duties as trained and assigned.Maintain a clean organized work area.follow oral and written instructions listed in the SOPS, Batch records and Protocols.work in a self-direct team orientated manufacturing environment. to meet medical requirements for personal protective equipment (PPE) required for the area.Magic leap:(August 2018, December 2018)Clean room manufacturing associateResponsible for performing production and engineering support activities within a Clean Room production environment.Perform daily metrology setup, calibration and obtain data for qualification (LTS / Long Term Stability) from four different work stations on a daily basis.Responsible for performing production and engineering support activities within a Clean Room production environment.Perform post station quality checks using customized equipment to identify misalignment, measure thickness, and gaps in the parts built.Responsible of performing daily preventive maintenance and set-up of an auto-loading machine, a robot and sealing tool.Use of caliper tool, and microscopes to ensure conformance to specifications.Handle chemicals and solvents following all safety protocols.Operate a custom-made Autoloader machine in both loading and unloading of parts.Monitors process and equipment and makes necessary adjustments to maintain work instructions specifications.Identify any non-conforming product, quarantine it or scrap it using custom-tailored manufacturing execution system (MES).Report process deviations, updates and equipment malfunctioning promptly to Supervisor.Perform machine troubleshooting using company provided tools and SOP.Perform end of line, optical performance test of finished parts.Perform pack out process.ERBA DIAGNOSTICS:(September, 2013-2018)Group leader (august, 2014- January 2015)Properly executes duties described in reagent Manufacturing SOPs, batch records and protocols.Responsible to run dispensing of chemistry products (kits).Perform proper training and qualifications for production personal.Organize a group of operators setting up materials, operating equipment and completing production tasks involved in the manufacturing, dispensing, labeling, packaging, movement and /or warehousing of company products.Assist with the cleaning and calibration of production equipment, and with maintenance of a clean and safe work environment.Complete and review required Manufacturing documents in accordance with GDP, company policies and procedures.Take appropriate safety precautions and effectively utilizes required personal protective and safety equipment for the specific department in which work is been done, ensure other group members do the same.Provide primary back up for manufacturing department supervisor.Production supervisor (January, 2015-May 2018)Prepare the production orders according to the planed schedule provided by the planning department.Supervise chemistry departement reagents, botteling, packaging.Verification and creation of the labels and the batch records prior production.Secure the materials and reagent needed for the orders using Netsuite to track all the components.Assign the operators to complete the orders according to the production priorities and incoming orders.Complete and sign the line clearance prior production Run according to QA proper procedures.Review batch records and make sure all the documents are signed and complete following the Good Documentation Procedures.Provide Quality Control Laboratory with samples in order to release the finish good product.Enter the order in the system after the products are released from the QC/QA.Perform the accountability of the batch.Perform inventory adjustment to keep track with the use of Material.Submit the products to the ware house for storage or shipment.Aveva/Apotex drug delivery system (January, 2009-september, 2013) Production InspectorLead a team in the packaging room and labeling of transdermal products.Follow and enforce CGMPS and SOPS.Perform continuous quality checks to assure product meet quality.Maintain and clean packaging area and equipmentDocument packaging steps performed in the batch records.Set up and operate packaging machine Document operational parameter for packaging equipment.Perform QC inspection of units and pouched units.Perform accountability calculations.Aids in the creation of batch records, and revision of SOPS.Write discrepancy report and investigations needed.Support the training department of training and qualifying new employees.Certification:CPR.OSHA.WASTE DISPOSAL.Ergo training.Hazardous training.5S Training.Safety training.SKILLSComputer, punctuality, great communication, initiative, dependable and team player.Languages: fluent in French, Arabic and English literate in Spanish.EDUCATIONKEISER University- Pembroke pines, FL.Associates of science, 2008. Dean list: 4.0 GPA.Two years of college, Jadida Morocco (History and geography) |
