Relocation Assistance Eligible:

Referral Payout Eligible:

Continue growing with our family. 

Our team members make it happen. If you want to continue to grow in a new role internally and see a position that looks right for you, we encourage you to apply!

Thanks for your commitment to Tyson Foods. 

Management Level:

To feed a changing world, it takes an incredible team. From the cutting board to the board room, every Tyson Foods team member plays an important role in our success. That’s where you come in. We are hiring immediately for a Food Safety Quality Assurance General Manager role.

Setting the table for your success:

At Tyson Foods, our team members’ health and wellness is very important to us. We believe in helping our team members thrive inside and outside of the workplace. That’s why we’re committed to providing a holistic benefits package that provides support for you and your family.

We invest in our team members and their success by providing resources like BENEFITS ON DAY ONE OF EMPLOYMENT and FREE EDUCATION!

Benefits include: medical/Rx, dental, and vision coverage; 9 paid holidays; 4 weeks paid vacation upon hire, plus earned time off; 401(k) with employer match; stock purchase program; and product purchase program.  We also offer CAREER GROWTH and much more!

SUMMARY: This location is part of our Prepared Foods Division and manufactures bacon! The Food Safety Quality Assurance General Manager is responsible for the daily management of all activities of the FSQA department to include food safety programs specification adherence and product quality for products within their assigned facility. In addition, the FSQA Manager will oversee all special projects as assigned, departmental budgets, turnover and safety.

RESPONSIBILITIES:

Production Oversight:

• Manage daily production practices, including the reception of raw materials.
• Ensure pre-operational and operational sanitation standards are met.

Quality Assurance:

• Oversee finished product quality and Food Safety Systems.
• Implement and enforce Tyson FSQA policies and procedures.
• Monitor verification and documentation for compliance with government regulations.

Program Development:

• Develop, implement, and maintain HACCP, HARPC, SOP, GMP, and SSOP programs.

Product Conformity:

• Ensure finished products align with customer specifications and label requirements.
• Report product issues and audit results to relevant stakeholders.

Customer Interaction:

• Interact with customers and their agents for product showings, plant tours, and audits.
• Address initial product runs and respond to quality-related customer complaints.

Microbiological Monitoring:

• Monitor microbiological results and conduct bacterial swabs.
• Generate shelf-life environmental graphs.

Research and Development:

• Conduct research and development activities to enhance food safety and quality.

Team Management:

• Select, train, and manage FSQA Supervisors and Technicians.
• Facilitate both Food Safety and Foreign Material teams at the plant.

Audit Management:

• Complete required internal, regulatory, and customer audits.

Inventory Control:

• Manage Hold Release inventories at the plant level in SAP.

REQUIREMENTS:

• Education: Requires broad knowledge in general professional or technical field. This knowledge is normally acquired through a bachelor s degree in an academic field directly related and essential to the job.
• Experience: Minimum 3 years of prior industry experience to fully grasp regulatory, production and manufacturing concepts preferred.  Experience with FDA and USDA regulated products.  SAP Experience a plus. 
• Computer Skills:  Standard computer skills required; generating spreadsheets and developing templates for use by plant management and corporate FSQA, sales and operations.
• Communication Skills: Excellent communication skills required, both written and verbal, demonstrating the proven ability to correspond with all levels - line team members to corporate management.
• Special Skills: Must have good problem identification and problem-solving skills. Must be able to work independently yet interact with many different facets within the organization and be the plant liaison to USDA.  HACCP Certified, PCQI Certified and SQF Certified preferred.
• Supervisory: Manage crewing labor and attendance of the FSQA department.
• Travel: 3-5 plus trips per year.

Work Shift:

Tyson is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will be considered without regard to race, national origin, color, religion, age, genetics, sex, sexual orientation, gender identity, disability or veteran status.

We provide our team members and their families with paid time off; 401(k) plans; affordable health, life, dental, vision and prescription drug benefits; and more.

Are you ready for what’s next?  

Come explore opportunities within Brunswick, a global marine leader committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond.  Brunswick believes “Next Never Rests™,” and we offer a variety of exciting careers and growth opportunities within united teams defining the future of marine recreation. 

Sea Ray Tellico Operation

Vonore, TN

Job Opening: Quality Engineer

Position Overview: The Quality Engineer (QE) role is responsible to pro-actively support development, implementation, and continuous improvement of the Tellico quality management system to ensure a consistently high level of performance within the facility and market segments that we participate.  The scope of the role will include activities spanning supplier quality, internal process control, and customer feedback.  The Quality Engineer will be accountable to help drive continuous improvement through the facility by analyzing quality data, prioritizing opportunities and leading improvement activities throughout the entire operations.

Roles and Responsibilities:

• Pro-actively facilitate the development of Quality Systems to provide consistent inspection and testing to meet company standards of good sound visual quality and functional reliability.
• This role will support both internal and external quality processes.
• Improve processes to reduce common cause variability and eliminate special cause by following Problem Solving techniques such as Six Sigma (DMAIC).
• Use of structured quality improvement tools including six sigma tools is required.
• Ensure appropriate collection of quality data, analyze the data for trends, identify corrective action opportunities, and drive corrective action activities.
• Interpret basic technical drawings including characteristics such as views, title blocks, dimensioning, tolerancing, etc. Interpret specification requirements in relation to product and process characteristics.
• Assist in the development, maintenance and reporting of quality measurements and analysis. Helps determine the adequacy and accuracy of quality standards. Where standards are not available, coordinates their development.
• Promote and ensure quality activities in manufacturing and support functions to assure that Quality Metrics improve.
• Facilitate and train employee groups on process improvement and waste elimination techniques.
• Lead teams in applying structured problem-solving methodology and tools to eliminate waste.
• Some common tools required to use are: Process Map, Pareto Chart, Trend Chart, Fishbone Diagram, 5-Why Analysis, Histogram, SPC, FMEA, 5S, Correlation Analysis, Error-proofing, and Control Plans.
• Investigate, analyze, and benchmark industry practices for process validation assessments.
• Accurately maintain company records and documents in accordance with policies and procedures.
• Actively support and lead our Corrective Action processes.
• Perform special assignments as required.

EDUCATION REQUIREMENTS:

• Bachelor’s degree in a related engineering field required although consideration will be given to individuals with commensurate marine experience

• Must be willing to complete additional advanced education/training courses as required.

PREFERRED QUALIFICATIONS/SKILLS:

• At least 3-5 years in a Quality or Manufacturing Engineering position required. Preferred time spent working in the marine industry.
• Hold a Six Sigma Green Belt or Black Belt or ability to acquire.
• ASQ Certified Quality Engineer certification (or equivalent) or ability to acquire.
• Must have working knowledge of CAR methodology, computer literate, root cause analysis, be able to apply inspection data for process control, process capability assessment, ISO quality systems, and SPC.
• Microsoft Word, Excel, PowerPoint, Project, Visio. Statistical software.
• Thorough knowledge of statistical process control, teaching skills, blueprint analysis, quality concepts, basic and advanced quality tools, and problem-solving techniques.
• Ability to lead, teach and motivate a team.
• Able to work a flexible work schedule when required.
• Organizational skills necessary to successfully manage multiple projects simultaneously.
• Ability to get along with diverse personalities while remaining tactful, professional, and flexible.
• Good written and oral communication to communicate with all levels of the organization.

Next is Now!  
We value growth and development, recognizing that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and inspiration. Therefore, we encourage people from all backgrounds to apply to our positions. Please let us know if you require accommodations during the interview process. 

Equal Opportunity Employer: Minorities/Women/Protected Veterans/Disabled

EEO is The Law - click here for more information

Brunswick and Workday Privacy Policies

Brunswick does not accept applications, inquiries or solicitations from unapproved staffing agencies or vendors. For help, please contact our support team at: hrsharedservices@brunswick.com or 866-278-6942.

All job offers will come to you via the candidate portal you create when applying through a posted position through https:///www.brunswick.com/careers.  If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at 866-278-6942 or HRSharedServices@brunswick.com.

Ihre Aufgabe

• Wahrnehmen der Product Center Verantwortlichkeiten für die Produktgrupp ‚PD-Lösungen‘
• Überwachungsaktivitäten der übergeordneten Produktqualität (über alle Standorte z.B. mittels globaler Besprechungen)
• Aufbereitung von Daten zu spezifischen Qualitätsereignissen
• Koordinieren der Kommunikation mit den internen und externen Interessenvertretern im Fall eines Qualitätsereignisses
• Aufbereiten von Reklamationsstatistiken (z.B. zur Unterstützung von PMS Aktivitäten)
• Mitarbeit an der globalen Harmonisierung von qualitätsbezogenen Prozessen und Testmethoden
• Schnittstelle zu den Qualitätseinheiten der relevanten Werke, zum Value Stream sowie anderen unternehmensweiten Funktionen
• Unterstützung der regulatorischen Funktionen zur Wahrung der Produktqualität/-konformität
• Unterstützung CAPA Management im Bereich Product Center Sterile Fluids
• Management globaler Änderungsprojekte mit regulatorischem Hintergrund

Ihr Profil

• Abgeschlossenes Studium (mind. Bachelor) im technischen oder naturwissenschaftlichen Bereich
• Erfahrung in einem Regulatory Affairs- oder Qualitätsumfeld im Arzneimittelbereich oder im medizinischen Bereich wünschenswert
• Kenntnisse im Bereich von Medizinprodukte- und Arzneimittelregelwerken (MDD, MDR, GMP, etc.) sowie Qualitätsmanagement- und Risikomanagementstandards (z. B. ISO13485, ISO14971, FDA 21 CDR §820, etc.) wünschenswert
• Sehr gute Englischkenntnisse in Wort und Schrift
• Sorgfalt, Eigeninitiative, Teamfähigkeit und Kommunikationsstärke runden Ihr Profil ab

Are you ready for what’s next?  

Come explore opportunities within Brunswick, a global marine leader committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond.  Brunswick believes “Next Never Rests™,” and we offer a variety of exciting careers and growth opportunities within united teams defining the future of marine recreation. 

Summary of Position: This 3rd shift position works with the V6/V8/V10 outboard assembly product lines and reports to the Quality Engineering Manager.  The main role of this position will be to maintain quality assurance procedures, practices, and standard evaluation methods, that will ensure product quality and integrity, and will minimize process variation.

Primary Duties and Responsibilities:

• Work individually or collaboratively to reduce manufacturing process or product variation, using laboratory instruments and equipment, along with root cause corrective action methods
• Lead or assist in formal problem-solving projects including completion of corrective action requests
• Look up engineering drawings on computers, read and understand tolerances and key product features
• Perform basic dimensional inspections of parts utilizing calipers, micrometers, and other hand-held gauges
• Recommend design changes or improvements in production methods through FMEA or other methods as appropriate
• Work with engineers, technicians, and operators to assist with training as required
• Support manufacturing's non-conforming material process as required, and identify scrap reduction opportunities
• Organize and assist in resolving quality spills, including part sorts, containment activities, and creating quality alerts
• Create visual aids to support operator instructions
• Perform internal process, product, and ISO audits as directed, to ensure assembly conformance to requirements
• Contribute to deviations, FMEAs, and other quality documents in the quality management system
• Clearly communicate quality standards on the production line and in toolbox meetings
• Clearly communicate quality concerns immediately to managers, supervisors, process techs, and operators
• Document quality issues through shift notes and hand off meetings
• Commitment to health and safety (both in the office, laboratory, and in the plant)

Knowledge, Skill and Ability Requirements:

• Possess a mechanical aptitude with the ability to reason through problems and suggest workable solutions
• Must be detail oriented, with the ability to pay very close attention to specifications
• Ability to perform basic mathematical calculations and basic statistics
• Proficient knowledge of PC software including Word, Excel, and Power Point
• Working knowledge of pertinent manufacturing assembly techniques
• Working knowledge of inspection techniques, metrology methods, and print tolerances
• Working proficiency in the use of inspection equipment such as micrometers, gauges, fixtures, etc.
• Possess both verbal and written communication skills to effectively present data and information to management
• Ability to guide supervision in making proper decisions relative to product and process control issues
• Self-motivated with the ability to learn and lead by example, utilizing a good work ethic and a positive attitude
• Excellent organizational, time management, communication, and follow-up skills
• Ability to perform duties independently, consulting supervisor for only occasional exceptions
• Ability to be flexible and able to manage diverse and/or changing priorities and assignments
• Ability to lead, work with, and instruct others in related job functions
• Willingness to work extended hours and weekends, per schedule and as needed

Education and Experience Requirements:

• High School diploma or GED required
• Associate degree or equivalent post high school combination of experience and relevant technical training
• Three or more years of experience with complex assembly operations in a manufacturing setting

Preferred Certifications:

• ASQ – Certified Quality Auditor, Quality Inspector, or Quality Technician is desired
• LSS Green Belt Certification desired

Preferred Qualifications:

• Associate’s or bachelor’s degree in manufacturing, engineering, science, or related field
• Demonstrated history of problem-solving skills and root cause analysis
• Ability to conduct mathematical calculations of moderate complexity
• Ability to organize data, perform statistical process analyses, and draw meaningful conclusions
• Ability to read and understand GD&T (Geometric Dimensioning and Tolerancing)
• Strong computer skills including knowledge of software such as Power BI and Power Apps
• Knowledge of manufacturing execution systems such as PINpoint or Rockwell Automation
• Knowledge of S.P.C. techniques
• Knowledge of quality tools including Process Mapping, PFMEA, Validation Studies, MSA, and Control Plans
• Experience in Lean Manufacturing and 5S
• Bilingual - ability to speak both English and Spanish

Next is Now!  
We value growth and development, recognizing that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and inspiration. Therefore, we encourage people from all backgrounds to apply to our positions. Please let us know if you require accommodations during the interview process. 

Equal Opportunity Employer: Minorities/Women/Protected Veterans/Disabled

EEO is The Law - click here for more information

Brunswick and Workday Privacy Policies

Brunswick does not accept applications, inquiries or solicitations from unapproved staffing agencies or vendors. For help, please contact our support team at: hrsharedservices@brunswick.com or 866-278-6942.

All job offers will come to you via the candidate portal you create when applying through a posted position through https:///www.brunswick.com/careers.  If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at 866-278-6942 or HRSharedServices@brunswick.com.

Relocation Assistance Eligible:

Referral Payout Eligible:

Continue growing with our family. 

Our team members make it happen. If you want to continue to grow in a new role internally and see a position that looks right for you, we encourage you to apply!

Thanks for your commitment to Tyson Foods. 

Management Level:

Please be sure to submit a resume in a Word or .pdf format.

SUMMARY: This position is responsible for the daily management of all activities of the FSQA department to include food safety programs specification adherence and product quality for products within their assigned facility. In addition, the FSQA Manager will oversee all special projects as assigned, departmental budgets, turnover and safety. 

Essential Duties & Responsibilities Include:

• Daily oversight of production practices including raw material receiving requirements; pre-operational and operational sanitation; finished product quality and Food Safety Systems; ensuring all Tyson FSQA policies and procedures are followed
• Monitoring verification and documentation associated with adherence to government regulations
• Developing, implementing and maintaining the HACCP, PCQI, SOP, GMP and SSOP based programs
• Ensuring finished product conforms to customer product and label specifications
• Report product issues and audit results to plant and corporate FSQA, plant management, corporate sales and/or operations
• Interacting with customers and their agents for product showings, plant tours and audits; visits to customer facilities
• Initial product runs and investigation response to quality related customer complaints
• Monitoring microbiological results; conducting bacterial swabs and generating shelf-life environmental graphs
• Performing research and development activities
• Responsible for implementing and maintaining food safety and quality programs and for the selecting, training and managing of FSQA Supervisors and FSQA Technicians
• Facilitating both the Food Safety and Foreign Material teams at the plant
• Completing required internal, regulatory, and customer audits
• Managing Hold Release inventories at plant level in SAP.

REQUIREMENTS:

Education: Bachelor’s degree or higher in food safety, animal science, natural science, or a related technical field, or equivalent job experience essential to the role.

Experience: 5+ years of industry experience, with 8+ years preferred. Experience with USDA regulated products is preferred, and SAP experience is a plus.

Computer Skills: Proficient in standard computer skills, including spreadsheet generation and template development for effective communication with plant management, corporate FSQA, sales, and operations.

Communication Skills: Exceptional written and verbal communication skills, demonstrating the ability to correspond effectively with team members at all levels, from the production line to corporate management.

Special Skills: Strong problem identification and problem-solving skills. Ability to work independently while effectively collaborating with various facets within the organization and serving as the plant liaison to USDA. HACCP Certified, GFSI Certified, and PCQI Certified are preferred.

Supervisory Skills: 2+ years of direct supervisory experience, with 5+ years preferred.

Travel: Occasional travel, approximately 2-5 trips per year.

Position Specific Requirements:

• Internal applicants should either upload a resume to their application in Workday OR complete their application fully showing current and past work experience OR make sure their Career Profile in Workday is up to date and complete.
• Must reside in the United States to be considered.
• Sponsorship is not available for this position.

Internal disqualifiers are the following:

• No more than 4 attendance points for locations on an 8 point policy
• No written warnings in the past six (6) months
• No suspensions on record for the last 12 months

Work Shift:

Tyson is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will be considered without regard to race, national origin, color, religion, age, genetics, sex, sexual orientation, gender identity, disability or veteran status.

We provide our team members and their families with paid time off; 401(k) plans; affordable health, life, dental, vision and prescription drug benefits; and more.

This role combines the Design Quality Assurance and the Product Center Manager role. In your role as Design Quality Assurance Expert (m/f/d) you will be working as a part of product development team on new product development or on design changes to ensure product quality and reliability, minimize risk to users and patients. In addition, the Product Center Manager's responsibilities are added to this position, which includes post-market surveillance tasks and ensuring regulatory compliance. This ensures that the entire life cycle of the product can be managed and controlled.

Your assignments

Design Control

• Ensure that all design control deliverables comply with applicable regulatory requirements and design control processes
• Guide engineering and other teams and ensure that design control requirements are being met in an effective manner to achieve quality by design, including those for design verification, validation, specification and procedure development, risk management, and design review
• Provide input to design and manufacturing engineering project DHF deliverables including material specifications, drawings, inspection procedures, and manufacturing procedures, to ensure that the resulting products can be adequately manufactured and tested. Review DHF files for accuracy and completeness and provide guidance on FDA compliance and procedures
• Work independently on high visibility new product development projects; including projects involving multiple technologies and design sites
• Create processes and process improvements to ensure consistent implementation of internal requirements and external regulations and standards

Product Conformity

• Main contact for medical devices marked with the CE-mark with a focus on non-active medical devices for Peritoneal Dialysis
• Ensure that Technical Files are complete and up to date and that essential requirements are met

Post Market Surveillance

• Analyze PMS data and if needed initiate required activities

NC/CAPA

• Acts as a Quality Approver for design control related topics and as a Quality Assignee for system related topics

Your profile

• Bachelor or master’s degree in engineering or a similar technical field required, such as medical technology or a technical apprenticeship with further training to be a technician, along with relevant professional experience
• Several years related experience or an advanced degree without experience
• Advanced knowledge of Design Control and Risk Management standards (e.g, ISO13485, IEC 60601 and ISO 14971)
• Advanced knowledge of medical device regulations (e.g. MDR 745/2017, 21CFR820.30, NMPA-Regulation)
• Experience with product or design and development or quality engineering of sterile disposables utilizing various plastic processes such as injection molding and extruding
• Deep understanding of Design Controls and solid engineering expertise that enables them to guide engineering teams
• Experienced with development of design input and traceability through verification and validation V&V activities
• Excellent presentation and communication skills, high engagement on achieving targets and ability to communicate technical information to non-technical audiences
• Willingness to travel national and international
• Fluent in written and spoken English and German

Classification:

Shift:

Job Description:

Are you looking for a new challenge? Passionate about innovation? Want to work for a company that values integrity, teamwork and loyalty?

At LATICRETE International we are driven to be a top ten construction chemical company that still values family, diversity, collaboration and invention. We’ve been in business for over 65 years, family-owned/operated for three generations and are available in 100 countries. In 2017, The Hartford Business Journal named us one of Connecticut’s Top Family-Owned Companies!

We don't just make innovative, industry-leading products. We strive to connect with, engage with and improve the lives of our employees, our customers, our partners, and the global communities in which we operate.

We are seeking passionate and ambitious employees who want to make a difference not just within our organization, but within their communities and the world. If that sounds like you, then what are you waiting for? Join the family and expand your horizons!

Just some of our benefits:

• Medical
• Dental
• Vision
• 401k
• Tuition reimbursement
• 12 paid holidays in addition to paid vacation and sick time
• Flexible spending
• Life Insurance, AD&D and Supplemental Insurance

Covid-19 Precautions:

At all of our facilities we are taking additional precautions with temperature checks, deep cleaning, testing, and work from home opportunities.

POSITION SUMMARY

The position is responsible for ensuring that all products manufactured meet or exceed quality standards as well as all safety, environmental and ISO requirements. Implement continuous improvement initiatives in the manufacturing and QC environment.

ESSENTIAL DUTIES AND RESPONSIBILITIES -

Additional duties and responsibilities may be assigned as necessary. 

1.   QC Lab and Process Management (80%):

• Knowledge of work instructions, procedures, and calibration of QC instrumentation referenced in the LATICRETE Quality Control Manual.
• Ensures all lab testing results are filed all the Quality Control test data and enter pertinent information (CofAs) into the computer database (JDE).
• Ensure QC testing samples are obtained according to the Quality Requirements testing Level (Work Instruction 9.1.36) and maintain a storage system for retained samples. 
• Monitors the execution of (G)ood (L)aboratory (P)ractices.
• Responsible for the entry of test results in the QC tracking system and the crosscheck of records.
• Has basic knowledge of 5S and can assist in training  new employees
• Orders supplies for the QC lab and ensures the QC data-up system is maintained and updated daily. 
• Assists in communications with production personnel to provide a smooth, efficient production flow of quality products, as needed.
• Ensures all QC instruments meet calibration requirements listed in the calibration work instructions.
• Works with team members to identify improved methods of QC analysis and/or new QC lab equipment to improve lab efficiencies.
• Ensure that all CoA's, MSDS, Calibration/Verification, meet ISO 9001 traceability.
• Complete and distribute all forms in accordance with the work instructions in the Q.C. Manual.
• Write a daily report of all QC testing performed on products received in the QC lab using the appropriate communication database or electronic format.
• Supports the root cause analysis investigation of nonconforming product
• Test and report on all Field Test complaints filed by technical services.
• Has the ability to provide improvements for QC lab workflow, testing, and other QC related activities
•  Compare all C of A’s against the Master C of A to determine acceptance or rejection and enter all pertinent data into the computer system

 Data Collection and Data Analysis (20%): 

• Demonstrates problem solver abilities, while communicating with superiors with appropriate solutions in a timely and efficient manner.
• Computer Skills: Strong knowledge of Microsoft Office (Word, Excel) and Outlook; and ability to present technical data to QC team, business leaders and others as needed.
• Team Cooperation – lead the LATICRETE core values by maintaining a positive, cooperative, and professional attitude with all LATICRETE Employees and all customers.
• Provide and ensure batch adjustments are meeting expectations; based on QC lab batches performed.
• Has a strong technical knowledge of chemistry in the following area(s): cementitious chemistry, epoxy liquids, latex, and/or any LATICRETE product lines.
• Provide data to Quality Control Champion and Regional QC Managers for monthly KPI reports

Quality Control Ways Of Working – QC WOW (Daily):

• Prioritize and allocate work:  Delegate and allocate tasks to lab personnel to support company priorities and drive results. Set clear priorities for team and individuals, including appropriate allocation of resources (time, money and people).
• Build Team Culture:  Consistently hold lab personnel accountable for upholding the organizations values.  Properly and timely escalation of unhealthy conflict among peers and lab personnel.  Foster an open environment where peers feel able to provide constructive feedback and suggestions for improvement. 
• Communicate and Motivate:  Communicate regular business updates.   Convey information in a clear and timely manner.  Listen carefully to the views and opinions of peers, lab personnel, and internal customers.    

REQUIRED SKILLS & QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education and Experience:

• Associates Degree in science or engineering or 3-5 years of QC laboratory experience

Specialized Skills and Experience:

• Computer Skills: Strong knowledge of Microsoft Office (Word, Excel) and Outlook; and ability to present technical data to QC team, business leaders and others as needed.
• Excellent organization skills, ability to manage multiple projects with competing priorities.
• Good verbal, written, and math skills.
• Strong analytical and problem solving skill.
• Organized and meticulous.
• Possess the ability to roll-up the sleeves and execute daily QC responsibilities as required.  
• May have strong technical knowledge or ability to leverage knowledge of chemistry in the following area(s): cementitious chemistry, epoxy liquids, latex, and/or any LATICRETE product lines.
• Demonstrated ability to provide improvements for QC lab workflow, testing, and other QC related activities – provide evidence of projects led
• Compare all C of A’s against the Master C of A to determine acceptance or rejection and enter all pertinent data into the computer system. 
• Ensures all QA requirements are met by the QC lab.    

Travel Requirement: 

•  Must be able to travel 0-5%.  

Physical Requirements:

• Must pass pre-employment physical. 
• Lift:   Must be able to lift and/or carry a minimum of 50 pounds. 
• Push/Pull:  Must be able to push/pull __50__ pounds.  
• Stand:  Must be able to stand __75__% of the day.
• Sitting:  Must be able to sit __25__% of the day.
• Twisting/Bending:  Must be able to twist/bend _25__% of the day. 
• Squatting, Climbing and/or Crawling:  Must be able to squat/climb/crawl __25_% of the day. 

#LI-DS1

品質管理エクセレンス課は、品質管理グループにおいて、ファイザーが出荷する製品の品質試験/評価が適切に実施されることを様々な側面から支援する役割を担っています。

既存システム/機器の最適化やメンテナンス、新規システム/設備/機器の導入による品質管理業務のDigitalization、安定性試験業務の管理、規格及び試験方法や試験記録などの文書管理、逸脱対応や変更管理、教育プログラムの管理、社内外の査察対応、品質管理業務全般の見直しなど種々の業務において、あなたの持つ専門知識や経験を通して、効率的かつ確実な品質管理基準の維持・改善に貢献頂ける方を募集します。

職務内容

１．主な職務における成果責任/ Description of Primary Role & Responsibility

品質管理エクセレンス課に属し、品質管理グループとして行うべき品質管理業務を的確に遂行する。或いは品質管理グループ全体のシステムや手順の改善を伴うロジェクト等を担当、管理する。

• 分析機器、ラボ施設、設備、ユーティリティーの校正や予防保全等の適正な維持管理
• Cycle Time削減・業務効率化につながるDigitalシステム/設備の導入や変更
• LIMS（ Laboratory Information Management System）及びラボ関連システムとデータの維持管理
• 安定性試験（新製品、既存製品、工程変更、逸脱対応）の管理全般
• 社内の規格及び試験方法の維持・管理・変更
• 製品品質照査の対応
• トラブル（工程異常、輸送時の逸脱、試験結果不適）逸脱事象への対応及び品質評価
• 依頼分析や検討試験に対する文書作成
• 教育カリキュラムやトレーニング、教育資料の管理及び整備
• 社内外の査察対応（準備、当日対応、指摘の是正処置や予防措置）を通じたコンプライアンスの向上
• 最新の薬機法、GMP及びData integrity要件を理解し、品質管理業務や手順に反映させる
• Pfizer社内基準など種々の要求事項に沿った手順の見直し・管理
• 継続的な業務カイゼン
• 安全衛生活動
• 特命事項への対応

２．応募資格/ Qualifications

【資格・能力要件/ Desired Behavioral and Technical Skills】

• 一般社員又は管理職
• 薬学、化学、化学工学など理系の大学程度の知識がある又は3年以上の製造関連業務或いは研究関連業務の経験があること
• GMPや日本薬局方、品質に関する規制要件やガイドラインについての十分な知識がある又は習得に意欲のある方
• 課員、社内外の関係者とのコミュニケーションを円滑に行える方
• 工場全体や所属部署の業務改善のための変化に対応できる又は意欲のある方
• 業務を行う上で十分な英語能力を有し、海外サイトと英語で適切にコミュニケーションができる、又は英語の規格及び試験方法などを読解し、海外とメールで情報共有する英語力があることが望ましい（TOEIC：730点以上又は600点以上）

【職務経験/Background requirement】

• 品質部門又は製造部門での十分な業務経験、或いは同等の知識や経験

以下経験があると望ましい/Nice to have

• 分析機器（HPLC,GC,UV,IRなど）や製造設備、Digitalシステムの導入に関わる業務経験
• 医薬品の分析若しくはそのデータレビューなど品質管理の業務経験、あるいは同等の知識・経験

【勤務地】　Japan - Nagoya Plant

Worker Type: Regular

Flex time: フレックス (日本)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

El Ingeniero de Calidad evalúa las operaciones, el proceso, y el producto para asegurar el cumplimiento de los estándares de calidad en el piso de producción, almacenes de materia prima, producto terminado y centros de distribución de la Organización. Determina en conjunto con el Ingeniero de Manufactura los criterios de calidad para la aceptación y rechazo del producto, atiende y resuelve problemas y tareas complejas mediante la interacción con los Supervisores, Líderes, Operadores de producción y otros miembros del equipo a través del uso de herramientas de Six Sigma, Lean Manufacturing, o de Solución de Problemas. Entre los métricos de interés para el ingeniero están los pizarrones de producción (indicadores), el seguimiento a las tareas de mejora continua, seguridad, calidad, costo, flujo del proceso y entrega a tiempo.

PRINCIALES RESPONSABILIDADES:

1. Optimización de los procesos de manufactura para la reducción de los PPMs internos.

2. Mejora sistemática de la habilidad de los procesos.

3. Cálculo de la capacidad del proceso (Cpk).

4. Liberación de los procesos productivos asignados tanto para producción regular como arranque de líneas y transferencias.

5. Liberación de productos y materias primas en SAP.

6. Contención y resguardo de materia prima, producto en proceso y producto terminado sospechoso y/o rechazado, en el área productiva y diferentes almacenes de la cadena de suministro al Cliente.

REQUISITOS:

1.-Licenciatura en Ingeniero Industrial, Mecánica, o afín.

2.-años como Ingeniero de Calidad.

3.-Toma de decisiones basado en datos, creatividad para la solución de problemas (Core Tools), estadística básica (gráficos XR, gage R&R, paretos, etc)., metrología básica, manejo de personal y proveedores, con sentido de urgencia.

4. Inglés 80%.  

5. Metodología para la solución de problemas.

6. Experiencia en Normas ISO 9001, 14000, OSHA 18000, IATF 16949.

7. Conocimientos generales en procesos de inyección y maquinados.

8. Conocimiento de herramientas Lean Manufacturing y Six Sigma.

9. Excelentes habilidades de comunicación oral, escrita, y manejo de la inteligencia emocional.

About Regal Rexnord

Regal Rexnord Corporation (“Regal Rexnord”) is a leading manufacturer of electric motors, electrical motion controls, power generation and mechanical power transmission products and sub-systems, serving customers around the world in the general industrial, consumer, commercial construction, food & beverage, and alternative energy end markets, among others. Regal Rexnord sells its products and solutions to OEMs, through distributors, and directly to end-users. Regal Rexnord is a $7.2B company with 36,000 associates globally.

You may not know it, but Regal Rexnord impacts your life every day. The company’s products enable the fans in HVAC systems that keep us comfortable; the power source that keeps smart buildings running; the agricultural and food service equipment that keeps us fed; and the conveyer systems that keep e-commerce flowing, to name a few of the applications where our products are used.

Regal Rexnord’s business purpose is to create a better tomorrow by energy-efficiently converting power into motion. This means creating innovative solutions while focusing on both customer needs and the company’s commitment to sustainability.  The company’s industrial powertrain and automation solutions offerings are an important part of the company's growth strategy. The company’s strategy includes leveraging 80/20 to prioritize all activities, including product excellence, operational excellence and commercial excellence (i) driving organic sales growth through the introduction of innovative new products, with a particular focus on improving energy efficiency, (ii) establishing and maintaining new customers, as well as developing new opportunities with existing customers, (iii) participating in higher growth end markets and geographies, and (iv) identifying and consummating strategic, value creating acquisitions.

Why Patients Need You

私たちの日々の業務はすべて、製品品質と患者さんへの安全で効果的な製品の提供に対する揺るぎないコミットメントに則したものです。私たちの科学的でリスクに基づく品質文化は、柔軟性があり、革新的で、顧客志向なものです。研究開発に関わっているかに関係なく、品質文化に対するあなたの貢献が患者さんに直接影響を与えることができます。

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

ファイザーの献身的で効果的な品質保証チームの一員として、ファイザーから出荷する製品の評価およびレビューを実施し、製品が適切に製造され、試験されていることを確認します。あなたの有する専門知識は、製品製造における基準からの逸脱を特定するのに役立ち、品質ポリシーへの準拠を確実なものにするために、逸脱や変更管理の承認を実施します。

あなたの持つ原則、考え、理論、問題解決スキルに関する包括的な知識を通じて、ファイザーは新しいマイルストーンを達成し、世界中の患者を支援する準備を整えることができます。

You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies.

Through your comprehensive knowledge of principles, concepts, theories of the discipline and problem-solving skills, you will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

名古屋工場で製造、検査、包装、試験される製剤について品質保証業務を行う。

• 国内外ならびにファイザーのガイドラインに沿った製造活動を管理・支援する。
• 国内外の行政ならびにファイザー社内の査察の準備ならびに対応を主導する。
• GMP文書、教育ならびにData Integrity強化活動を推進およびサポートを行う。
• 行政登録に必要な薬事対応や輸出関連の書類作成を行う。
• 品質問題、CAPA、ロット処置の決定に対して効果的な管理を主導する。品質、技術面で複雑な案件を含む。
• その他、工場内のGMP活動（逸脱処置、変更管理、業者管理、バリデーション）全般のサポート

Perform Quality Assurance tasks for drug products manufactured, inspected, packaged and / or tested and supplied from the Pfizer Global Supply Nagoya site including but not limited to:

• Managing and supporting manufacturing activities in line with domestic and international and Pfizer guidelines.
• Leading preparation and taking actions for domestic and international government and Pfizer internal inspections.
• Promoting and supporting GMP Documentation Control, Training, Change Management and Data Integrity enhancement activities.
• Creating pharmaceutical regulatory affair documents necessary for administrative registration to domestic and exported countries.
• Driving effective management of quality issues and Corrective Action Plan (CAPAs) and make decisions that may involve complex quality and technical issues.
• Support for all other GMP activities (Deviation Management, Change Control, Vendor Management, Validation).

Qualifications

Must-Have

• 学士号
• 3年以上の製薬業（製造部門または品質部門）での就業経験
• 品質保証業務を行うために必要なGMPに関する知識を有すること
• 業務に対する積極的な姿勢とクリティカルシンキングスキルを有すること
• 組織の一員として、部門メンバーと協力して業務を行える協調性があること
• 十分な文章力、コミュニケーション力があること
• 日本語及び英語でのコミュニケーション（メール、テレカン等）が取れること
• Bachelor's Degree
• 3+ years' experience in pharmaceutical manufacturing/Quality experience
• Current Good Manufacturing Practices experience with compliance issues resulting from cGMP deviations or product defects, regulations as related to vendor management programs and other industry quality systems and processes
• Proactive approach and strong critical thinking skills
• Strong collaboration, relationship management, and interpersonal skills
• Excellent written and verbal communication
• Communication in English/Japanese (E-mail, Teleconference, etc.)

Nice-to-Have

• 修士号
• Master's degree

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Are you ready for what’s next?  

Come explore opportunities within Brunswick, a global marine leader committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond.  Brunswick believes “Next Never Rests™,” and we offer a variety of exciting careers and growth opportunities within united teams defining the future of marine recreation. 

The Supplier Quality Supervisor – Non-Metallic will drive process and product improvements, support new product development, and lead APQP processes. This role will serve as the subject matter expert who will collaborate and guide engineering development, ensure appropriate GD&T, develop inspection setups with suppliers, and lead design for manufacturing activities.

This role involves all supply management and manufacturing aspects, including supplier grade development, supplier quality program development, and oversight. The candidate should have proven analytical, project management, personnel management, and interpersonal skills.

Job responsibilities are highlighted below.

• SME for non-metallic processes, with a focus on injection molding and SMC, familiar with mold design, GD&T and application for inspection setup and tolerancing of molded components or assemblies.
• Oversee the entire life cycle of suppliers' non-metallic projects, from conception to production (including AAR of Class-A surfaces).
• Use statistical tools (DOE, MSA/Gage R&R, Process capability, and Statistical Process Control) to drive process and product improvements.
• Make/suggest improvement ideas to suppliers' molding processes to reduce cycle time and eliminate waste and scrap without sacrificing part quality.
• Act as the primary point of contact between Mercury suppliers, tool makers, procurement, engineering and manufacturing operations to investigate and resolve supplier quality issues
• Lead cross-functional teams, facilitate and improve the Advanced Product Quality Planning (APQP) process with suppliers, including tool/fixture makers and from initial design stage through PPAP submission and the start of production.
• Serve as a technical resource for new business quoting activities, providing valuable insights and expertise into tooling and gages, create project schedules and monitor associated supplier progress to program deliverables.
• Perform supplier audits and site inspections; develop process improvement plans and drive implementation; drive long-term preventative actions.
• Lead supplier DFMEA activities, design reviews, PFMEA and process development as part of early supplier engagement to ensure manufacturing needs are considered in the design phase and proper quality expectations are defined.
• Lead and develop a team of quality engineers

Required qualifications:

• Minimum of 7+ years of hands-on experience in plastic injection molding, SMC molding, or mold-making processes ideally in a Supplier Quality, Quality Engineering or Manufacturing Engineering role
• Good understanding and strong knowledge of GD&T, tolerance analysis, stress analysis, mold flow analysis, DFM, etc.
• Strong analytical abilities, technical writing abilities and comprehensive understanding of quality tools (IATF 16949, statistical methods, MSA, FMEA, DOE, etc).
• Ability to read and interpret schematics/drawings and an in-depth knowledge of the application of quality standards and specifications.
• Experience with cosmetic classifications and understanding of process parameters that affect cosmetic defects (Appearance/AAR, Class-A surfaces)
• Detail-oriented with a focus on delivering high-quality results.
• Demonstrated leadership in driving successful project outcomes.
• Ability to work collaboratively in a fast-paced, dynamic team environment.
• The ability to provide solutions that reflect an understanding of business objectives and cost implications.

Preferred Qualifications:

• Strong understanding of polymer rheology and test methods such as DSC, TGA, and physical testing
• Experience with failure analysis using advanced techniques.
• Recognized as a technical expert in Plastics Engineering
• The ability to provide solutions that reflect an understanding of business objectives and cost implications.
• Direct experience or advanced training applicable to the processing of thermoplastics and/or extruded materials in a production environment
• Experience in supporting product and process development through the product lifecycle and associated assets.
• Experience with supply chain/Procurement, APQP/PPAP
• Certification through ASQ, LSS, PMI, or other applicable recognized organizations

Education Requirements:

• Bachelor of Science Degree in Engineering-
  • Plastics/Polymer Processing is preferred
• Supply Chain/procurement management experience is a plus
• APQP/PPAP knowledge is a plus

Business Travel Expectations

Potential to travel 25-45% on a short- or long-term basis depending on project phase and level of supplier support required

Next is Now!  
We value growth and development, recognizing that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and inspiration. Therefore, we encourage people from all backgrounds to apply to our positions. Please let us know if you require accommodations during the interview process. 

Equal Opportunity Employer: Minorities/Women/Protected Veterans/Disabled

EEO is The Law - click here for more information

Brunswick and Workday Privacy Policies

Brunswick does not accept applications, inquiries or solicitations from unapproved staffing agencies or vendors. For help, please contact our support team at: hrsharedservices@brunswick.com or 866-278-6942.

All job offers will come to you via the candidate portal you create when applying through a posted position through https:///www.brunswick.com/careers.  If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at 866-278-6942 or HRSharedServices@brunswick.com.

Company: Nissan Motor (Thailand) Co., Ltd.

Working Location: Nissan Manufacturing Plant 2, Bangna-Trad KM.22, Samut Prakarn, Thailand.

Hiring Condition: Permanent

Job Description

• Investigate and take countermeasure in part of vehicle quality.
• 4M change validation on process and product vehicle confirmation.
• Cooperate with shop floor and related function by cross-functional for solving the concern, find out root

• cause and take robust countermeasure.

• Specification checks on vehicle and validate in system.
• Facility and machine problem analysis and validate process.
• Support TQM and GEMBA management  

Qualifications

• Male/Female, 25-30 years old, Bachelor's/Master's Degree Mechanical/ Industrial Engineer.
• Experience 3-5 years in automotive QA or related fields (Automotive factory).
• Good skills in communication and interpersonal
• English language (TOEIC 500 up).
• Engineer thinking logical, good learner, open mild and good mindset
• Computer : Space vision, Auto CAD, DWG, Microsoft office
• Good interpersonal relations, positive thinking, punctual, responsible and ability to work under high pressure

If you are interested in this job role, please prepare your updated resume or LinkedIn profile for the application process through the Nissan Job Portal.

“Only shortlisted candidate will be contacted for an interview”

For more information about Nissan's products, services, and commitment to sustainable mobility, visit nissan-global.com. You can also follow us on Facebook, Instagram, Twitter and LinkedIn and see all our latest videos on YouTube.

Why Nissan?
You will definitely get the right answers why you should join us through watching the video on YouTube.

Are you ready for what’s next?  

Come explore opportunities within Brunswick, a global marine leader committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond.  Brunswick believes “Next Never Rests™,” and we offer a variety of exciting careers and growth opportunities within united teams defining the future of marine recreation. 

The Sr. Supplier Quality Engineer provides strategic and tactical support to Manufacturing by executing quality activities; such as:  advanced quality planning to support High Performance Product Development (HPPD) process, Supplier development activities, Corrective Actions, and reporting to maintain and improve customer satisfaction, eliminate errors and improve efficiency.  As a result, the Procurement Team depends on the Sr. Supplier Quality Engineer to be fully engaged with the global supply base to ensure that all direct purchased materials meet all performance specification requirements and do so over time to eliminate line downs, recalls, or other quality failures resulting in customer dissatisfaction.

Tactical Supplier Quality:  15%

Independently, and in collaboration with assigned suppliers within the global supply base, process and execute quality activities.  Maintain effective business communications/relationships with suppliers and internal customers to understand any quality impacts to production to proactively disseminate relevant information to all stakeholders and meet customer expectations and business requirements.  

Factory Support:  20%

Independently, and or in collaboration with others, exercise functional knowledge to effectively and efficiently execute business processes that ensure the support of ongoing production and supplier communications.  Passionately lead fellow employees by communicating the vision, engaging employees and empowering them to become change agents who are prepared and able to successfully lead the organization forward to embrace the future.

Supplier Development: 50%

As assigned and in collaboration with others, initiate projects, communicate project updates, identify barriers to project success and implement project plans to provide support to the organization’s objectives and supplier development goals.  

Process Management:  10%

Independently, and or in collaboration with others, exercise functional knowledge to effectively and efficiently execute business processes that ensure the absolute accuracy of system information and supplier communications. 

Continuous Process Improvement: 5%

Independently and/or in collaboration with internal and external working partners, define, measure, analyze, improve and control processes, programs and supplier performance to effectively, efficiently and proactively achieve strategic business initiatives and/or key performance indicators.

Experience / Professional Credentials:

• 7 + years of experience in manufacturing, operations, quality engineering
• Embedded control module design and validation
• Wiring harness and connector design and validation
• Preferred experiences with:
  • Electronic visual displays
  • Low Voltage and High Voltage wiring harnesses
  • PCBA’s (Printed Circuit Board Assemblies)
  • Battery Management Systems (BMS)
  • Power Distribution Units (PDU)
  • Electric motors: high and low  voltage, brushed and brushless
  • Alternators
  • Sensors
  • Ignition coils
  • Solenoids
  • ECM/ECU’s (Engine Control Modules/Units)
  • Knowledge of microprocessors, embedded electronics and prior experience in working on systems with multiple microprocessors and associated software complexity.
  • Electronics manufacturing process - SMT process, Through hole process Manufacturing Inspections AOI and 3D Xray.
  • Familiarity with software tools like ASPICE and AUTOSAR a plus
• ASQ certified Quality Manager, Engineer, or Auditor is preferred
• Lean six sigma Green or Black Belt certification with project experience is preferred

Education Requirements:

• BS/BA in Electrical/Electronic Engineering/Computer Science or a related technical field is required

Business Travel Expectations

• This position will require occasional day and/or overnight travel by auto or airplane, up to 30%.

Next is Now!  
We value growth and development, recognizing that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and inspiration. Therefore, we encourage people from all backgrounds to apply to our positions. Please let us know if you require accommodations during the interview process. 

Equal Opportunity Employer: Minorities/Women/Protected Veterans/Disabled

EEO is The Law - click here for more information

Brunswick and Workday Privacy Policies

Brunswick does not accept applications, inquiries or solicitations from unapproved staffing agencies or vendors. For help, please contact our support team at: hrsharedservices@brunswick.com or 866-278-6942.

All job offers will come to you via the candidate portal you create when applying through a posted position through https:///www.brunswick.com/careers.  If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at 866-278-6942 or HRSharedServices@brunswick.com.

Come Join Innovate Motion with Us!

Johnson Electric is excited to announce we are now recruiting for a Sr. Quality Engineer at our Zacatecas, Mexico facility.  This position will develop processes and systems to monitor and improve our production performance, with a goal of zero defects and the achievement of world-class supplier status.

Your responsibilities will be:

• Develop, control, and maintain the Control Plan.

• Review of Inspection Instructions.

• Follow-up to SPC of production line.

• MSA compliance of production line.

• Creating and revalidating PPAPs.

• Participation in the development and monitoring of APQPs.

• Perform risk analysis on the released product.

• Know and comply with customer requirements (CSR) and those applicable to ISO 9001, IATF 16949 and ISO14001.

Our requirements:

• Bachelor’s degree in engineering (electrical, mechanical, industrial, or equivalent).

• Advanced English communication skills.

• Data analysis skills, such as trending, confidence intervals, SPC, basic statistical analysis.

• Knowledge of Core Tools, GD&T, CSR, and special processes (applicable CQI)

• Knowledge of IATF 16949

• 7+ years’ experience in value-added automotive assembly.

• 7+ years’ experience supporting new product development in automotive manufacturing setting.

• Experience with Ford (Tier 1)

• Relocate to Zacatecas

What we offer:

• Attractive salary & benefits plan

• Relocation bonus (if applicable)

• International work environment

• Opportunities to be trained in China.

Come join our global, inclusive & diverse team

Our purpose is to improve the quality of life of everyone we touch through our innovative motion systems. We are a truly global team bound together by our shared values. Our culture is built on the diversity, knowledge, skills, creativity, and talents that each employee brings to the company. Our people are our company’s most valuable asset. We are committed to providing an inclusive, diverse and equitable workplace where employees of different backgrounds feel valued and respected, regardless of their age, gender, race, ethnicity or religious background. We are committed to inspiring our employees to grow, act with ownership and find fulfilment and meaning in the work they do.

Company: Nissan Motor (Thailand) Co., Ltd.

Working Location: Nissan Manufacturing Plant 1, Bangna-Trad KM.21, Samut Prakarn, Thailand

Hiring Condition: Permanent

Job Description

•  Investigate incident concern, root cause (4M) and create effective C/M of concern.
• Cooperate with related function for implement effective C/M and monitor result.
•  Support approval new methodology 4M / 4M change evaluation & confirmation
• Summary report Part Quality Assurance engineering activity and progress result to CE, MGR,AGM,GM
• Communicate & negotiate by English

Qualifications

• Bachelor's/Master's Degree Mechanical/Industrial Engineer.
• Experience 3-5 years in automotive QA or related fields (Automotive factory).
• Technical knowledge ex. Stamping of Metal sheet, welding, Automotive body part would be advantage
• Good skills in communication and interpersonal, English language (TOEIC 500 up).
• Engineer thinking logical, open mild and challenge to learn new things.
• Computer : Space vision, Auto CAD, DWG, Microsoft office
• Good interpersonal relations, positive thinking, punctual, responsible and ability to work under high pressure

If you are interested in this job role, please prepare your updated resume or LinkedIn profile for the application process through the Nissan Job Portal.

“Only shortlisted candidate will be contacted for an interview”

For more information about Nissan's products, services, and commitment to sustainable mobility, visit nissan-global.com. You can also follow us on Facebook, Instagram, Twitter and LinkedIn and see all our latest videos on YouTube.

Why Nissan?
You will definitely get the right answers why you should join us through watching the video on YouTube.