Process Engineer - #Guaymas

Chromalloy Gas Turbine Palm Beach Gardens , FL 33418

Posted 2 weeks ago

Date: 3/6/2019

Job Category: Engineering

Location: Guaymas, Mexico

Title: Process Engineer - #Guaymas

About Chromalloy:

Chromalloy is an integrated solutions provider for original equipment manufacturers, commercial airlines, militaries, oil and gas companies, and power companies, delivering innovative solutions to reduce manufacturing and operating expenses and extend the life of gas turbine engines. With locations in 11 countries, Chromalloy provides coatings, authorized repairs, castings and manufacturing overhauls, partnering with manufacturers and operators alike to provide the latest, most technologically advanced solutions.

Chromalloy is a subsidiary of Sequa Corporation. Sequa Corporation is a diversified industrial company with operations in the aerospace, metal coatings and automotive industries. Sequa is a Carlyle Group company. For additional information, visit www.sequa.com.

Description:

Currently, we are seeking qualified candidates for a opening to join our Engineering organization.

Day to Day:

Chromalloy is a global supplier of advanced repairs and services for gas turbines used in aviation and land-based applications and repairs. The company refurbishes and manufactures engine components, and designs and manufactures FAA-approved replacement parts for aircraft engines that are certified to meet or exceed the performance, reliability and durability specifications of original equipment manufacturer parts. In support of land-based vehicles, Chromalloy employs identical engineering disciplines used to produce its FAA-certified parts. Chromalloy serves commercial, military and industrial turbine engine operators worldwide.

PRIMARY DUTIES AND RESPONSIBILITIES:

  • Interacts with internal and external work groups to exchange information and resolve problems of typical scope.

  • Represents organization as prime customer contact with proven technologies.

  • Develops solutions to problems of typical scope and complexity.

  • Responsible for a significant portion of project work which must be completed in a manner which avoids serious program delays and excess expenditures.

  • Plans work schedule and defines resources for a work group.

  • Participates in project selling efforts.

  • Communicates with customer and completes/supports FAIR activities with QE's

  • Wide application of standard principles and working knowledge of related disciplines. Complex work is subject to minimal review.

  • Skilled with required technical design and analysis tools.

  • Coordinates with QE any corrective and preventative actions using technical analysis

  • Works from limited general/verbal or written direction.

  • Expresses issues and concerns to peers, supervision and management.

  • Delivers presentations to external customers.

  • Participates in supplier management and development.

  • Reviews and approves documents prepared by others.

  • Monitors work operations of some team members with well-defined tasks.

  • May interview and evaluate entry level applicants.

  • Leader of small teams.

  • Manages difficult scenarios of schedule, personnel, customer expectation and resulting business impact.

  • Leads procedures writing for established products/processes.

What you will do:

What you need to succeed:

Additional Information:

Bachelor's degree in Mechanical or Industrial Engineering required.

Experience in Aerospace Industry, with exposure to customers that Manufacture Aircraft Engines.

Knowledge of ISO/AS9102

CAD experience, including 3D modeling and generation of 2D engineering drawings (UG/NX experience is a benefit).

Knowledge on manufacturing processes: Grinding, EDM, TIG Welding and CNC programming

Knowledge of cores tools (PPAP, PFMEA, Control Plan, MSA, FAIR)

Knowledge on Times and motion studies

Improving of Health and safety conditions

Knowledge of lean manufacturing techniques, basic knowledge of Six Sigma methodology.

Proactive, supportive, and good attitude to improve current processes

Work under pressure

Ability to provide training for production operators

Bilingual: English-Spanish

Computer skills: MS Office software, ERP Software

Limitless Opportunities

Chromalloy has big plans for the future, just like you. We recognize that it takes planning and hard work to get there. So we offer challenging assignments, great teams, development and training, and exciting opportunities to enhance your skills, abilities and knowledge.

Chromalloy maintains a drug-free workplace and performs pre-employment substance abuse testing and background checks. Please note that depending on the specific position, you may be required to pass additional medical tests, background checks, and/or other requirements. These additional items are required for the company to comply with various laws and regulatory rules.

Apply only for positions for which you are qualified. If your work experience, skills and background are incompatible with the requirements of the job, you will not be considered for it.

Chromalloy is proud to be an Affirmative Action/Equal Opportunity Employer. Chromalloy participates in E-Verify. It is our policy to provide equal opportunity to all employees and applicants and to prohibit any discrimination because of race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or protected veteran status. Employees will be treated on the basis of their job-related qualifications, ability and performance. It is also our policy that sexual harassment or any other kind of harassment, including harassment based on sexual orientation, will not be tolerated. The foundation of these policies is our commitment to treat everyone fairly and equally and to have a bias-free work environment.

If you are a qualified individual with a disability or a disabled veteran and need a reasonable accommodation to use or access our online system or need to apply in an alternate way, please contact the Human Resources department at the individual business unit or annex. The telephone number for a specific business unit or annex can be found at Chromalloy Locations.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Senior Quality Engineer

Johnson & Johnson

Posted 5 days ago

VIEW JOBS 3/22/2019 12:00:00 AM 2019-06-20T00:00 DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, provides one of the most comprehensive orthopedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit www.depuysynthes.com. As a Senior Quality Engineer you will maintain a leadership of Quality and Compliance related projects. Leadership role for the development, implementation and maintenance of Quality System requirements on assigned areas of Manufacturing, Supplier management, Process Validation and New Products Introduction. Areas of responsibility may include: Non-conforming product, CAPA, Calibration Systems, Supplier Auditing, Sterility, Measuring techniques, tools and gages, Training, Statistical Support, Quality Planning, Experimental Protocols, Facilitation of Root Cause analysis, Risk Assessment and Complaint Investigation. Additional Responsibilities: * Areas of responsibility may include: non-conforming product, CAPA, calibration systems, supplier auditing, sterility assurance, and improving measuring techniques, design of gages, training, statistical support, quality planning, experimental protocols, and facilitation of root cause analysis, risk assessment and complaint investigation * Demonstrate ability to act as a technical reference. Lead, plan and implement special projects including continuous improvement activities, new technologies to support inspection and testing, statistical applications and periodic status reporting in assigned areas of responsibility. * Organize meetings and activities to provide guidance to other quality engineers, technicians or inspectors on reaching established goals. * Provide training and support to Quality Engineers on assigned areas. * Know and follow all laws and policies that apply to one's job and maintain the highest levels of professionalism, ethics and compliance at all times. * Diligently participate in our compliance program- related activities as denoted by your supervisor or our Chief Compliance Officer * Be a member of the Material Review Board (MRB). * Communicate and resolve quality issues and apply root cause analysis to drive corrective and preventive actions. * Work on continuous improvement activities. These may include participating in, and/or leading Quality Improvement Teams. * Provide quality reports and review trending on assigned areas of responsibility. * Conduct failure investigations and problem analysis regarding customer complaints, stock evaluations, supplier quality issues, calibration out of tolerance conditions, and CAPAs (internal or audit CAPAs). * Review and approve documents and drawings for manufacturing and product development (DCOs, MCs). * Support to Engineering, Manufacturing, Materials, Inspection, Distribution and/or Product Development Groups in order to assure quality and compliance of products. * Participate on cross- functional project teams. * Design gauging and develop tools and techniques to measure product parameters to assure product complies with engineering drawings. * Recommend, acquire and validate the necessary tools, equipment and technologies to support inspection and testing activities. * Develop and document Quality Plans to support product acceptance activities. * Facilitate creation of risk management documents. * Ensure compliance issues are addressed for product activities. * Participate on design reviews and risk analysis for product changes. * Provide process validation program oversight to ensure adequacy of validation activities and documentation in terms of regulatory compliance and technical/statistical soundness. * Review, assess and evaluate validation protocols (IQ, OQ, PQ) for compliance to procedures and regulations, statistical validity and approval. * Provide guidance to others for the generation of clear, concise and defendable protocols and reports. * Assist in determination of the need for validation. * Generate and/or maintain internal validation master plans as required. * Manage process monitoring activities including tracking, data collection and analysis, corrective action, and reporting. * Manage supplier validation activities including supplier assessment, protocol development, and generation of supplier validation master plan(s). * Lead continuous improvement activities for the validation program to ensure efficiency, effectiveness and compliance. * Coordinate and participate on supplier audits and technical assessments. * Assist purchasing with identification and qualification of suppliers and alternate manufacturing locations. * Administrate Supplier Management Program and measures effectiveness. * Manage Supplier CAPA activities including root cause analysis, definition of corrective actions and verification of actions. * Coordinate Quality Plans and inspection/test methods between suppliers and Synthes. * Visit suppliers for the purpose of quality issues investigation and capability analysis. * Assist purchasing in resolution of supplier complaints Qualifications * A minimum of a Bachelor's degree in Sciences, Business, Engineering or related technical field is required * A minimum five (5) years relevant experience in Quality, Manufacturing or Product Development Engineering is required * Experience managing multiple projects/requirements in a fast-paced environment is required * Experience working in the medical device/diagnostic/pharmaceutical OR a regulated industry is required * Knowledge of FDA's QSR and ISO regulations is preferred * Root Cause Analysis experience is preferred * Working knowledge of Geometric Dimensioning and Tolerancing, Blueprint Reading, Basic Metrology, Gage design, Design/Process FMEA and Quality Plan Development is preferred * Knowledge of Gage Repeatability and Reproducibility, Statistical Process Control, Process Capability and Design of Experiments is preferred * Certification in ASQ Certified Quality Engineer, Lean Manufacturing and/or Six Sigma certification is preferred * Knowledge of Manufacturing materials and removal processes (machining, sheet metal, electro polishing, passivation, hard coating, cleaning, adonization, etc.) is preferred * This position will be located in Palm Beach Gardens, FL and may require up to 25% travel including potential international travel Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Primary Location United States-Florida-Palm Beach Gardens- Organization Depuy Orthopaedics. Inc. (6029) Job Function Quality (Eng) Requisition ID 6509190204 Johnson & Johnson Palm Beach Gardens FL

Process Engineer - #Guaymas

Chromalloy Gas Turbine