Sergio Olivas's Location
Houston, Texas, United States, United States
Sergio Olivas's Contact Details
Sergio Olivas work email
- Valid
- Valid
- Valid
- Valid
Sergio Olivas personal email
n/a
About Sergio Olivas
I am a Mechanical Engineer with 15 years of experience focusing in the manufacturing industry. My objective is to obtain a position in a world-class organization which will utilize my expertise in engineering design, quality management and manufacturing. I am looking to assume increasing responsibility within a team that rewards initiative, commitment and personal productivity.
Sergio Olivas's Current Company Details
Emerson
View
Quality Manager at Emerson Automation Solutions
- Website:
- emersonindustrial.com
- Employees:
- 10
- Company phone:
- +1.314.679.8984
- Company email:
- inquiries@emerson.com
Sergio Olivas Work Experience Details
-
Quality ManagerEmerson Apr 2018 - PresentSt. Louis, Mo, Us
-
Quality ManagerEmerson Sep 2020 - Dec 2020St. Louis, Mo, Us
-
Senior Supplier Performance EngineerEmerson Jun 2018 - Aug 2020St. Louis, Mo, UsPlan, coordinate, and lead supplier evaluation and approval activities. Perform regular supplier audits to ensure compliance with Rosemount Emerson and regulatory standards.Technical liaison between suppliers, purchasing, engineering, and operations.Communicate Rosemount Emerson supplier performance expectations to suppliers.Develop quality plans, inspection plans, and material incoming verification methods.Initially qualify or disqualify suppliers utilizing the AQP process for current parts and for Supply Chain parts (ES Events, Cost Reductions, R&D etc.).Work with commodity team to development and implement supplier management programs. Establish and maintain successful relationships with suppliers, commodity team, operations, and design engineersParticipate in NPD process to help ensure design for manufacturability (DFM.) Develop and maintain department quality documentsLead drawing reviews for purchase parts in order to reduce risk , develop Procurement Specifications.Establish, monitor, and take appropriate action in response to KPI’s.Work with both global and local suppliers to ensure expectations are clear and use established quality control processes to ensure quality performance is met.
-
Sr Quality EngineerCantel Medical Jan 2017 - Jun 2018Little Falls, Nj, Us-Quality liaison for NPD for single-use endoscope valves,-Design and specify inspection and testing procedures to ensure medical devices conform to specifications and quality standards.-Investigate/analyze in-house and field failures (customer complaints) and monitor quality trends.-Led in house and customer investigations for non-conformant products.-Revamped manufacturing validation procedures to ensure all activities conform to ISO-13485 -Introduced an Incoming Inspection Procedure along with test procedures for different components (fabrication, plastic, tubing, etc.) used to manufacture medical devices.-Represent Quality Assurance on product development teams to develop Risk Management Plans.-Analyzed product data and recommended improvements for product line, led data management activities and monitored the CAPA system. -
Supplier Quality EngineerAlcon Oct 2011 - Feb 2016Geneva, Switzerland, ChLead Supplier Quality Systems audits to determine capability and compliance for incoming components.Partnered with supply chain for new supplier selection and approval activities.Work actively with suppliers for new products components development.Perform prospective supplier’s systems and technical capability evaluations and lead supplier selection process.Monitor supplier key performance indicators (KPI’s)Oversee supplier Corrective and Preventive Actions (CAPA’s) to ensure timely and thorough investigation responses.Principal liaison between suppliers and Alcon for quality and technical issues.Partnered with multiple departments to resolve production issues ranging from supplier related non-conformances and customer complaints. -
Product EngineerAlcon Mar 2009 - Oct 2011Geneva, Switzerland, ChProvide support required for the manufacturing of ophthalmic surgical devices by creating and interpreting documentation required for product assembly, inspection testing and processing.Contributed in the transfer of labor intensive assemblies to a lower cost manufacturing center. Implemented labeling requirements per EN980:2008 standards for all surgical products.Manage design initiated projects to for new or current products.Evaluated and implemented to completion supplier initiated changes for current components.-Accellent Endoscopy Juarez, Mexico
-
Program EngineerInteger Holdings Corp. (Formerly Lake Region Medical) Sep 2006 - Mar 2009Wilmington, Massachusetts, UsDeveloped and coordinated the implementation of pFMEA’s and Control Plans for all plastic injection components used in the fabrication of medical devices.Managed engineering changes and initiated the quoting process for new tooling opportunities, engineering changes, and customer driven tool repairs.Responsible for new program implementation from Design Review to approval and qualification of plastic components used in the fabrication of medical devices.Managed cross functional teams for new programs implementation.Managed equipment and processes programs transfers for the plastic injection molding room increasing capacity, efficiency and reducing the machine hour rate by 25%. -
Component Engineer (Supplier Quality)Johnson & Johnson Nov 2004 - Sep 2006New Brunswick, Nj, UsEnsuring the constant flow of conforming components to production on a timely manner working with the second largest plastic supplier.Analyze/Monitor tooling capital for new and existing instruments.Evaluated tooling associated with each program for production capacity and capability making recommendations to the company and suppliers.Manage Design Change Plans and Engineering Changes to components in order to improve quality and reduce product costs.New tool qualifications ensuring quality through DOE’s.In charge of tool transfers between different suppliers ensuring a smooth transition from sampling stage to production.-Nypro (Plastic Injection Molding -
Manufacturing EngineerNypro Dec 2003 - Nov 2004St. Petersburg, Florida, UsEvaluated tooling associated for assigned customers for production capacity and capabilities making recommendations to the customer as necessary.Managed engineering changes, initiating quoting process for new tooling opportunitiesImplemented Single Minute Exchange Die program (SMED) in order to improve tool set-up procedures which led to a lead time reduction of 50%, increasing productivity on two 390 ton presses which are dedicated to one customer.Continuous participation in corrective actions reviews and implementation of resultant plans for improvement.Developed new procedures and manufacturing cells in order to improve efficiency and reduce head count. -
Mechanical Product EngineerPhilips Jan 2000 - Aug 2002Amsterdam, Noord-Holland, NlNew product introduction technology, Liquid Crystal Display (LCD) monitors from design center to the manufacturing plant within the assigned time frame, working closely with suppliers in order to achieve costs reductions of $150,000.Responsible of technical support of production lines and to improve line capacities and efficiencies by utilizing tools such as root cause analysis, statistical methods (SPC, CP/CPK, SE) and design of experiments (DOE).Tested, evaluated and re-specified material and parts in order to achieve a 10% cost reduction, (i.e.-molded parts, metal stamping, corrugated).In charge of generating Bill of Materials (BOM), Process and Routings for new products.Implemented engineering design changes (ECN’s) that improved product quality, reliability and efficiency while complying with customer’s specifications.Managed engineering changes, initiating quoting process for new tooling opportunities
Sergio Olivas Skills
Design Of Experiments
Capa
Quality System
Medical Devices
V&v
Iso 13485
Validation
Fda
Design For Manufacturing
Design Control
R&d
Fmea
Sergio Olivas Education Details
-
The University Of Texas At El PasoMechanical Engineering
Frequently Asked Questions about Sergio Olivas
What company does Sergio Olivas work for?
Sergio Olivas works for Emerson
What is Sergio Olivas's role at the current company?
Sergio Olivas's current role is Quality Manager at Emerson Automation Solutions.
What is Sergio Olivas's email address?
Sergio Olivas's email address is se****@****son.com
What schools did Sergio Olivas attend?
Sergio Olivas attended The University Of Texas At El Paso.
What skills is Sergio Olivas known for?
Sergio Olivas has skills like Design Of Experiments, Capa, Quality System, Medical Devices, V&v, Iso 13485, Validation, Fda, Design For Manufacturing, Design Control, R&d, Fmea.
Who are Sergio Olivas's colleagues?
Sergio Olivas's colleagues are Jason Hidalgo, Khoa Trieu, John Weet, Po-Yuan Huang, Corey Lucas, Erick Perez, Seth Dornak.
Free Chrome Extension
Find emails, phones & company data instantly
Find verified emails from LinkedIn profiles
Get direct phone numbers & mobile contacts
Access company data & employee information
Works directly on LinkedIn - no copy/paste needed
Aero Online
Your AI prospecting assistant
Select data to include:
Total price:
$0.00
0 records × $0.02 per record
Download 750 million emails and 100 million phone numbers
Access emails and phone numbers of over 750 million business users. Instantly download verified profiles using 20+ filters, including location, job title, company, function, and industry.
Start your free trial